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High blood pressure signs : The worrying symptom in your eyes that could signal your risk – Express

February 14th, 2020 4:48 am

High blood pressure relates to ones force of blood against the arteries. The force is a result of the blood pumping out of the heart and into the arteries as well as the force created as the heart rests between heartbeats. When the blood moves through the body at a higher pressure, the tissue that makes up the arteries will begin to stretch and will eventually become damaged. This leads to many problems over time with the condition then affecting the eyes.

High blood pressure can occur after the blood pressure has been consistently high over a prolonged period of time.

A persons blood pressure levels can be affected by a lack of physical activity, being overweight, having a diet with too much salt or leading a stressful lifestyle.

If left untreated, a blood pressure of 180/120 or higher results in 80 percent chance of death within one year, with an average survival rate of ten months.

Prolonged, untreated high blood pressure can also lead to heart attack, stroke, blindness and kidney disease.

READ MORE: How to live longer: The best diet proven to increase life expectancy and ward off cancer

Spotting the early warning signs of the dangerous condition is crucial and developing this symptom in your eyes could mean youre at risk of developing high blood pressure.

If a person has high blood pressure left untreated it may cause a hypertensive crisis.

A hypertensive crisis is divided into two categories: urgent and emergency.

In an urgent hypertensive crisis, the good pressure is extremely high, but the doctors dont suspect there has been any damage to the organs.

In an emergency hypertensive crisis, the blood pressure is extremely high and has caused damage to the organs.

Signs of a hypertensive crisis may include severe chest pain, severe headache and nausea.

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What is hypertensive retinopathy?

The retina is the tissue layer located in the back of the eye.

This layer transforms light into nerve signals that are then sent to the brain for interpretation.

When blood pressure is too high, the retinas blood vessel walls may thicken. This may cause the blood vessels to become narrow, which then restricts blood from reaching the retina.

In some cases, the retina becomes swollen.

Over time, high blood pressure can cause damage to the retinas blood vessels, limit the retinas function and put pressure on the optic nerve, causing vision problems and potentially leading to blindness.

This condition is called hypertensive retinopathy.

Symptoms include reduced vision, eye swelling, bursting of a blood vessel or experiencing double vison accompnaied by headaches.

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Eye doctor leads the way to children’s clearer vision across the Caribbean – University of Miami

February 14th, 2020 4:48 am

A University of Miami ophthalmologist is spearheading an effort to improve pediatric vision screenings in the Caribbean Basin.

A few years ago, Dr. Alana Grajewski was having dinner with an ophthalmologist visiting the University of Miamis Bascom Palmer Eye Institute to train with her in pediatric glaucoma surgery, when he admitted a realization he had in the operating room earlier that day.

The physician from the South American coastal nation of Suriname was unsure he would even get a chance to perform the techniques Grajewski had taught him because some children show up to his office in such poor condition that it is too late to repair their vision. If left untreated, glaucoma can cause blindness in children.

Although the message was disheartening, after the doctors confession, Grajewski began researching the problem more. She learned that vision impairment and blindness is four times higher in the Caribbeanalthough in South America, Suriname culturally is considered to be a Caribbean nationthan it is in the United States, and she saw an opportunity to help.

In the Caribbean, there is very little that has been done in the way of identifying childrens eye disease early, and if you dont identify these problems, it becomes a more expensive and more damaging problem down the road, said Grajewski, who has been treating children as an ophthalmologist for 30 years and who directs the Samuel and Ethel Balkan International Pediatric Glaucoma Center at the Bascom Palmer Eye Institute. But if you are able to catch something and fix it, youre improving their ability to function in school and in the world.

Starting with Suriname, Grajewski is now leading an effort called the Pediatric Preventable Blindness (PPB) initiative to help eradicate vision loss in children. Currently, there is no formal vision screening in Suriname until children reach the age of 5. Yet by working with her colleagues at Bascom Palmer, other U.S. experts in the fields of ophthalmology and public health, as well as the University of Suriname, Grajewski came up with a strategy to screen childrens vision earlierby doing it when they get their vaccines. If it is implemented fully, this model would allow Suriname doctors to mitigate vision problems before they worsen, she said.

The Caribbean loves this concept, Grajewski added. When we presented our model at a recent ophthalmology conference at the University of West Indies, ophthalmologists throughout the Caribbean were thrilled.

With early detection and treatment, more children who need glasses at an early age will be able to get them, and children with more severe vision impairments like pediatric glaucoma can be referred to an ophthalmologist, said Matthew Javitt, research fellow. With surgery, pediatric glaucoma has an 80 percent to 90 percent chance of restoring a childs vision. And with the vision screening model Grajewskis team designed, it will only add four minutes to a familys vaccination appointment.

The PPB initiative began with a trip to Suriname last May when Dr. Christina Dowell, a resident at the University of Miami Miller School of Medicine, visited several clinics and trained health care workers in how to use vision screening equipment. For children younger than six months, an arc light is used, which is a device that can be attached to a mobile phone to take a photo of the eye and detect any abnormalities. For children older than six months, a device called a spot vision screener is used to detect any impairments. While she was there, Dowell visited clinics near the countrys capital of Paramaribo with Dr. Denise Doelwijt, a University of Suriname ophthalmologist, and trained health care workers on how to conduct vision screenings. In July, another team from Bascom Palmer visited four clinics in Suriname. At the end of this month, Doelwijt, along with Bascom Palmer researchers Dr. Eleonore Savatovsky and medical student Adriana Grossman, are planning to expand their reach to visit 17 clinics across the country.

We were looking to put a screening in as part of the existing infrastructure, which was why we chose the vaccination process where there is 95 percent participation from parents in Suriname, said Javitt, who helped develop the initiative.

As Surinames only current pediatric eye surgeon, Doelwijt is often inundated with young patients who have not even gotten an eye screening when they arrive in her office. In December, she had a six-month wait to see new patients, she reported.

This will make the wait time a little shorter because children will have already been screened elsewhere, she said.

Doelwijt is a surgeon at the Suriname Eye Centre, which is part of the academic hospital for the University of Suriname. She has gathered a team of medical students and is collaborating with Grajewski to implement the initiative at an expanding number of clinics across the nation of more than 500,000 people. Doelwijts students also will help University researchers collect data that can evaluate if the initiative is improving the diagnosis process. However, Doelwijt is confident the model will help Surinames physicians.

If this can help us operate earlier on the kids who need it, patients would get a better visual end result, she said.

Since vision develops in the brain from what a child can physically see, Doelwijt and Grajewski said that the faster vision problems are corrected, the best chance a child has to either improve his or her vision or avoid blindness. Children grow into their vision, so if they are seen later, or not evaluated properly, they can still develop poor vision even if they have a beautiful eye, Doelwijt said.

After a model is working in Suriname, Grajewski wants to implement a similar PPB program in Trinidad, Jamaica, and Barbados through the Universitys new partnership with the University of the West Indies.

In December, Bascom Palmer hosted a conference for physicians from across the hemisphere to learn about the initiative and discuss ways to implement a similar model in other countries that need a better way to conduct vision screenings. Ophthalmology experts from several universities in the region attended to learn about the initiative.

Once its in place, this effort will be self-sustainable and will be part of the policy in these countries, said Grajewski.

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Barton Foundation gives over $360000 to community health improvements – South Tahoe Now

February 14th, 2020 4:48 am

Jenna Palacio, Barton Health

SOUTH LAKE TAHOE, Calif. The Barton Foundation provided more than $360,000 in funding during 2019, delivering a profound community impact made possible by philanthropy and donor generosity over the year. Medical equipment, new technology, care provider education, and support, expanding access to mental and behavioral health services, and funding for local organizations were all aspects of the Barton Foundations scope of giving last year, as part of its commitment to community well-being through Barton Health.

More than one-third of the Barton Foundation investments in 2019 went to purchasing medical equipment, bringing in new technology, and offering training and education opportunities for care providers. Some of the new equipment and technology upgrades include an additional infant warmer in the Barton Family Birthing Center; a specialized camera to detect retinopathy the leading cause of blindness in the United States; ventilators to support patients with chronic respiratory conditions at home; and medical technology to allow for sharper images guiding wrist and hand orthopedic surgeries.

Bartons 2018 Community Health Needs Assessment identified mental and behavioral health as the most pressing health issue of the area. The Barton Foundation dedicated sizable funding in 2019 to community organizations working to address this issue. Additional support provided by the Foundation last year went to improving access to mental and behavioral health services, and renovating two Emergency Department rooms at the hospital for patients in crisis.

As part of the Barton Foundations vision to positively impact the health of the community by providing financial resources, funding was given to an array of local support, education and health improvement efforts. Financial aid was given to cancer patients for access to Bartons Cancer Support Services. The Foundations 2019 grant cycle awarded $50,000 to 15 local care-based organizations. Further training and medical equipment was given to community police, fire, and educators for the Stop the Bleed program, which trains first responders how to care for trauma victims.

The Barton Foundations mission is to inspire philanthropy for the health of the community. Up next in the Barton Foundations annual programming, Pink Heavenly will take over Heavenly Mountain Resorts California Base Lodge on March 21, celebrating fundraising efforts that directly benefit wellness programs through Bartons Cancer Support Services.

For more information, giving, and upcoming events with the Barton Foundation, visit bartonhealth.org/foundation.

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Sophie Wessex to spend Valentines Day APART from Prince Edward – because of the Queen – Express.co.uk

February 14th, 2020 4:48 am

Sophie, who married Prince Edward in 1999, is set to leave the beloved members of her family behind tomorrow, her royal diary shows. According to the official royal schedule, the Countess of Wessex will visit Germany on Valentines Day, representing the Queen.

This means Sophie will have to skip Valentines Day celebrations this year.

Her husband, the Earl of Wessex, is attending an event in Harrogate today, and doesnt look set to have any engagement lined up in Germany over the next few days.

Following her day in Germany, Sophies diary is free of engagements until February 26.

This is likely due to the fact that the Countess children, Lady Louise Windsor and James, Viscount Severn, are on their half-term break and Sophie wants to spend as much time as possible with them.

Upon returning to work, Sophie will attend a reception at St Jamess Palace for the International Agency for the Prevention of Blindness in her role as Global Ambassador.

The prevention of blindness is one of the main areas of interest of Sophies royal work, together with female empowerment.

READ MORE:Sophie, Countess of Wessex: How did she assert self as royal?

While Sophie and Edward dont look set to spend Valentines Day together, the couple will likely delay the celebrations and carry them out during the weekend.

Edward is the Queens youngest child and the only one out of the monarch and Prince Philips four children who didnt get a divorce.

Sophie and Prince Edward met at a tennis match in 1993 and dated for six years before tying the knot at St Georges Chapel, the same church where Meghan Markle, Princess Eugenie and Lady Gabriella Windsor got married between 2018 and 2019.

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The Wessexes nuptials were televised, and as many as 200 million viewers from all over the world tuned in to witness their love.

Ahead of his big day, Prince Edward said: We manage to have a good laugh about things most of the time, and we happen to love each other, which is the most important thing of all.

While Sophie and Edward may be spending tomorrow apart, other royals look set to show their romantic traits to their other halves.

According to royal expert Katie Nicholl, Prince William is a romantic deep down and he will likely use tomorrow as an excuse to spend more time with Kate, Duchess of Cambridge.

Ms Nicholl told OK! magazine: Kate and William are clearly very happy in their marriage and it shows.

Theyre both affectionate and these days theyre not afraid to show that in public.

Theres a very natural chemistry and warmth between them.

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Sophie Wessex to spend Valentines Day APART from Prince Edward - because of the Queen - Express.co.uk

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Doctors team up with students to improve cervical cancer treatment – Baylor College of Medicine News

February 14th, 2020 4:47 am

For women with advanced cases of cervical cancer, radiation therapy is generally the only curative treatment. The treatment of cervical cancer is unique, in that, brachytherapy, a form of radiation treatment where radioactive isotopes are placed within or near tumors, is a necessary component.

Dr. Michelle Ludwig, a radiation oncologist at the Dan L Duncan Comprehensive Cancer Center at Baylor College of Medicine, and Dr. Alexander Hanania, fourth-year resident physician in radiation oncology at Baylor, both see patients at Harris Health Systems Attwell Radiation Therapy Center at Smith Clinic. They are researching a way to make brachytherapy more efficient and less toxic for patients with cervical cancer.

Cervical cancer is a disease more common in medically underserved patients who have less access to screening and vaccination, Ludwig said. We are excited to work to bring access to personalized medicine in the form of a customizable device to the medically underserved patients in Harris County, as we have one of the highest volume centers in the country for this patient population.

Reserved solely for the most technical and challenging of cases, a procedure called interstitial brachytherapy allows doctors to deliver higher doses of radiation internally and directly to the tumor.

Interstitial brachytherapy is generally only needed for patients with large advanced tumors, or when there is another reason such as anatomical challenges or disease recurrence, Hanania said. In certain areas where we treat the uninsured population, more often than not, were seeing locally advanced disease, which often requires interstitial brachytherapy.

Historically, the procedure involves suturing a grid template to the body, then inserting a series of needles through the template holes and into the tissue involved with and surrounding the tumor. Radioactive isotopes are run through the needles to deliver the radiation and kill the tumor.

The procedure is highly effective in controlling and often curing cervical cancer that has not spread to other parts of the body, but it can also be damaging to the tissues and organs surrounding the cervix. According to Hanania, new devices on the market allow for more precise treatment but most are too expensive for most hospitals.

Last fall, Hanania visited Rice University with the hopes of finding an affordable solution. He presented the problem at an engineering design fair where students met with potential collaborators in a variety of industries. He met a group of five undergraduate students seniors Elisa Arango, Susannah Dittmar, Krithika Kumar and Sanika Rane and junior Lauren Payne all interested in addressing a global health issue.

We know that the women affected by cervical cancer have less access to healthcare, Dittmar said. These women shouldnt have to go through this painful, extensive treatment just because of their financial situation. We wanted to find a way to make the procedure better.

The group, which calls themselves Team At Your Cervix, got to work designing a new obturator that could be built with a 3D printer at Rices Oshmann Engineering Design Kitchen. After months of research and collaboration with Ludwig and Hanania, they now have a prototype called the Universally Friendly Obturator, or UFO.

Our goal was to reduce the number of transcutaneous needles, Dittmar said. The way were going to do that is by bringing them into the obturator so theyre going through the vaginal canal and not through the tissue.

The UFO is also wider than a traditional obturator and has a flexible head so the needles can better reach the cervix without disturbing the surrounding tissue.

Our goal was for it to be 3D printed so it can be an open sourced file, Payne said. Because were a global health project, it has to be low cost. The idea is that anyone in the world can access the file and print it.

In the coming months, the group will continue to develop and test new prototypes. They have designed simulations to see how the device would hold up in a real procedure

I think this device could decrease the morbidity of the implant. If its effective, it will not only shorten the amount of time that were in the operating room, it will also decrease the amount of trauma to the body, Hanania said. Every needle you put in increases the risk of trauma to other nearby parts of the body. This device would work with existing technology to make the therapy more targeted, and therefore less toxic.

The group will present their final prototype at the Rice Engineering Design Showcase at Tudor Fieldhouse on Thursday, April 16. After graduation, the team hopes another group of seniors will continue their work.

Dr. Hanania and Dr. Ludwig came to us with an actual problem that they face, said Rane, who will be attending Baylors School of Medicine in the fall. Our prototype can have an immense effect here in Houston and across the globe.

-By Molly Chiu

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Life Sciences Jobs Expected to Grow by 133,000 Over Next 10 Years in the UK – BioSpace

February 14th, 2020 4:47 am

Are you in the United Kingdom and looking for a job in the life sciences? Or, are you planning on having a career in the life sciences? If so, then, youll be happy to know that there are an expected 133,000 jobs to be added to the sector over the next 10 years.

A new report called the Life Sciences 2030 Skills Strategy published in collaboration with theAssociation of the British Pharmaceutical Industry and the U.K.s Office for Life Sciences, forecasts the addition of 133,000 life science jobs by 2030. The jobs will range across the sector and include biopharma, medical devices and other areas of the industry. Specifically, the report predicts the addition of 43,000 jobs in biopharma, about 90,000 jobs in medtech and another 55,000 jobs to replace retirees across the sector.

The forecast does get a little more specific for the types of positions that will be needed in the U.K. over the next 10 years. For example, the report suggests that pharma research and development will require about 19,300 positions, while manufacturing roles in pharma will grow by about 6,400 jobs. While those are strong numbers, the report suggests that the medical device industry will see even greater growth.

The report projects 8,000 new jobs in medtech research and development and 46,500 jobs in medtech manufacturing.

For the other positions, the report suggests that by 2030, there will be an increase of 52,400 service and supply positions in the industry.

Alex Felthouse, managing director, Eisai Manufacturing and chairman of the Science Industries Partner Futures Group, a participant in the survey, said the strategy guide lays out the recommendations to take skills forward out to 2030 in support of the growing life sciences industry

To meet the demand that we have for the future we need to ensure that our industry is attractive to those who are considering joining the sector. We need to make them aware of all of the fantastic opportunities there are across a diverse and exciting range of activities from research and development through to medicines manufacturing. We also need toensure we have parity of esteem between different educational routes whether it be traditional academic routes, apprenticeships, vocational studies or ongoing continued professional development.

In order to capture some of these positions, the Life Sciences 2030 Skills Strategy outlines some of the key skills that will be needed by applicants. The skill sets include, as could be expected, proficiency in computers, as well as statistical literacy. The skills outlined are broad, but with the increasing reliance on machine learning and artificial intelligence in the pharmaceutical industry, that should provide more direction for potential applicants. The report notes that there is an accelerating convergence between life sciences, computer science, mathematics, statistics, engineering and chemistry in the fields of diagnostics, personalized medicine and data science.

There are also a number of soft skills that will be of benefit for future applicants. According to the survey, those kinds of skills will involve effective communication, leadership skills, sales and marketing abilities, as well as translational commercialization skills.

With the projected growth of jobs over the next 10 years, Nadhim Zahawim, business and industry minister for the U.K., said the government of the United Kingdoms hope is that the country will become a science superpower. By creating cutting-edge jobs in the life sciences industry, that will help the U.K. make progress in areas such as early medical diagnosis and manufacturing, Zahawim said in a statement. By providing a pathway for the growth, Zahawim said this will help level up every part of the UK with new opportunities.

In order to meet the demands, the government made several recommendations, including the implementation of an action plan from key stakeholders to oversee the growth of the industry. This action plan is aimed at encouraging and incentivizing the take-up of apprenticeships programs in all parts of the sector in order to establish parity of esteem with academic routes. Additionally, the action plan calls for supporting the transfer and exchange of a global workforce. The action plans have yet to be finalized, but when they are, the government said it will establish certain as-yet unnamed milestones and targets.

The government also points out that it will need to promote science, technology, engineering and mathematics programs to boost the increase of potential applicants, and also create a positive landscape that will attract and retain globally mobile talent. The strategy also notes that encouraging some academic researchers to shift into industry will also be key.

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AI IN MEDICAL DIAGNOSIS: How top US health systems are reacting to the disruptive force of AI by revolutionizi – Business Insider India

February 14th, 2020 4:47 am

AI is rocking medical diagnosis with its potential to incite drastic improvements to hospital processes. AI can process images and patient health records with more accuracy and expediency than humans are capable of, lessening physician workload, reducing misdiagnosis, and empowering clinical staff to provide more value.

While early moving hospitals are already extracting value from AI in medical diagnosis, most US hospitals are at the very early stage of the AI transformation curve - and they risk falling behind if they don't move now.

In this report, Business Insider Intelligence examines the value of AI applications in three high-value areas of medical diagnosis - imaging, clinical decision support, and personalized medicine - to illustrate how the tech can drastically improve patient outcomes, lower costs, and increase productivity.

We look at US health systems that have effectively applied AI in these use cases to illustrate where and how providers should implement AI. Finally, we examine how a leading US health system validates AI partners and internally organizes its AI strategy to offer provider organizations a template for AI innovation.

The companies mentioned in this report are: Aidoc, Allscripts, Amazon, Arterys, Boston Gene, Cabell Huntington Hospital, Cerner, Cleveland Clinic, Epic, Geisinger Health System, Google, HCA Healthcare, IBM, iCAD, IDx, Intermountain Healthcare, Johns Hopkins, Meditech, Microsoft, Mount Sinai, NorthShore University HealthSystem, Oak Street Health, Stanford University, Tempus, UCI Health System, Unanimous AI, Verily, Viz.ai, and Yale New Haven Hospital.

Here are some of the key takeaways from the report:

In full, the report:

Want to learn more about the fast-moving world of digital health? Here's how to get access:

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North American Prostate Cancer Market scrutinized in the new analysis – WhaTech Technology and Markets News

February 14th, 2020 4:47 am

North American Prostate Cancer Diagnostics and Therapeutics Market Size, Share & Trends Analysis Report by Diagnostic Technique (Prostate-Specific Antigen Test, Digital Rectal Examination, Prostate Biopsy, Imaging Techniques) by Therapeutics (Hormonal Therapy, Chemotherapy, Immunotherapy, Radiation Therapy, Targeted Therapy, Surgery) and Forecast 2019-2025

North American prostate cancer diagnostics and therapeutics market is expected to grow at a CAGR of 10.4% during the forecast period. The major factors for the growth of the market include the high prevalence of prostate cancer in the region which raises the demand for efficient diagnostics and therapies for the treatment of cancer.

As per World Health Organization, in the North America, prostate cancer is the most prevalent cancer among men. Around 234,000 new cases of prostate cancer has been registered in 2018 in the region.

Additionally, in 2018, around 18.5% of the total cases of cancer are related to prostate cancer in the US. Moreover, the adoption of innovative technologies for the diagnosis of prostate cancer such as biomarkers and the adoption of personalized medicine for treatment is expected to fuel the market.

Report: http://www.omrglobal.com/requesttic-market

North American prostate cancer diagnostic market is divided on the basis of diagnostic technique and therapeutics. By diagnostic technique, the market is segmented into prostate-specific antigen test, digital rectal examination, prostate biopsy, imaging techniques.

Prostate biopsy is expected to hold a major market share during the forecast period. By therapeutics, the market is segmented into hormonal therapy, chemotherapy, immunotherapy, radiation therapy, targeted therapy, surgery.

During the forecast period, chemotherapy is expected to have a major market share in the region. Geographically, the market is divided into the US and Canada.

The US is expected to hold the major major market share during the forecast period.

Report: http://www.omrglobal.com/industrtic-market

North American Prostate Cancer Market Segmentation

By Diagnostic Techniques

By Therapeutics

Regional Analysis

Company Profiles

Report: http://www.omrglobal.com/report-tic-market

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CRISPR ‘minigene’ used to prevent genetic liver disease in mice – Drug Target Review

February 13th, 2020 12:49 pm

Researchers have developed a new CRISPR technique, using a minigene, which was inserted into mouse DNA, resulting in improved liver disease symptoms.

In a proof-of-concept study, researchers have successfully used a new CRISPR gene-editing technique in mice to prevent a genetic liver disease known to be driven by hundreds of different mutations and improve clinical symptoms.

According to the scientists, from Penn Medicine, US, the findings suggest a promising CRISPR tool that could potentially treat patients with a rare metabolic urea-cycle disorder caused by a deficiency in the enzyme ornithine transcarbamylase (OTC), as well as other hereditary diseases triggered by different mutations on the same gene.

The CRISPR approach was developed from a previous one created at Penn Medicine which was limited to correcting only one mutation and benefitted new-born mice but not adults. This time, the technique, which employs a novel, dual adeno-associated virus (AAV) to deliver its components, inserted a minigene into the genome to accomplish a sustained expression of OTC in liver cells. No mutations are corrected; instead, a new set of instructions are added to the cells. As a result, researchers observed a clinical benefit in new-born mice that was maintained in adulthood.

Like most genetic diseases that present lethal effects in new-borns, early treatments that are effective for the long term are essential, said Dr James Wilson, a professor of Medicine, and director of the Gene Therapy Program and the Orphan Disease Center at Penn. Here, we moved a CRISPR approach forward to not only sustain expression of OTC in the cells but also broaden the tools abilities.

To develop a broadly applicable genome-editing tool, the team constructed a new, dual AAV vector containing an RNA-guided bacteria protein called Cas9. Known as AAV8, this Penn-developed vector specifically has an affinity for liver cells. The second AAV contained a fully functioning minigene expressing a codon-optimised human OTC, the donor DNA, driven by a liver-specific promoter to ensure it only expresses in liver cells when injected into the blood.

The first step the researchers took was to create a break in the DNA by Cas9 at the targeting site along the gene, which enables the addition of the minigene for homology directed repair (HDR).

Unlike other CRISPR approaches that delete or modify a portion of the normal gene, this technique integrates a new portion, said first author Dr Lili Wang, a research associate professor of Medicine. Were not trying to correct mutations that stop liver cells from producing OTC, were adding this new minigene so the cells can.

we moved a CRISPR approach forward to not only sustain expression of OTC in the cells but also broaden the tools abilities

Mice treated with the targeted vector showed 25 and 35 percent of OTC-expressing cells in the liver at three and eight weeks, respectively. This is four- and three-fold higher than the mice treated with the untargeted vector. At both three and eight weeks, most OTC-positive liver cells were located in clusters scattered throughout all portions of the liver in the targeted mice.

Researchers also observed a 60 percent reduction in ammonia levels in targeted mice compared to untreated mice fed on a high protein diet, a clinical sign that suggests the liver cells are producing OTC.

With these successful animal studies, weve moved closer to a potential broad spectrum gene-editing approach to treat patients with the OTC deficiency, irrespective of mutation and clinical state, Wilson said. The next step, through additional pre-clinical studies, is to find a safe harbour site on the gene in human liver cells and then to test a similar gene-editing approach.

The results were published in Science Advances.

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We’ve Sequenced the Human Genome. So Why Haven’t We Cured More Diseases? – Discover Magazine

February 13th, 2020 12:49 pm

An emergency room physician, initially unable to diagnose a disoriented patient, finds on the patient a wallet-sized card providing access to his genome, or all his DNA. The physician quickly searches the genome, diagnoses the problem and sends the patient off for a gene-therapy cure. Thats what a Pulitzer prize-winningjournalist imagined2020 would look like when she reported on the Human Genome Project back in 1996.

The Human Genome Project was an international scientific collaboration that successfully mapped, sequenced and made publicly available the genetic content of human chromosomes or all human DNA. Taking place between 1990 and 2003, the project caused many to speculate about the future of medicine. In 1996, Walter Gilbert, a Nobel laureate,said, The results of the Human Genome Project will produce a tremendous shift in the way we can do medicine and attack problems of human disease. In 2000, Francis Collins, then head of the HGP at the National Institutes of Health,predicted, Perhaps in another 15 or 20 years, you will see a complete transformation in therapeutic medicine. The same year, President Bill Clintonstatedthe Human Genome Project would revolutionize the diagnosis, prevention and treatment of most, if not all, human diseases.

It is now 2020 and no one carries a genome card. Physicians typically do not examine your DNA to diagnose or treat you. Why not? As I explain in a recentarticle in the Journal of Neurogenetics, the causes of common debilitating diseases are complex, so they typically are not amenable to simple genetic treatments, despite the hope and hype to the contrary.

The idea that a single gene can cause common diseases has been around for several decades. In the late 1980s and early 1990s, high-profile scientific journals, including Nature and JAMA, announced single-gene causation ofbipolar disorder,schizophreniaandalcoholism, among other conditions and behaviors. These articles drewmassive attentionin thepopular media, but weresoonretractedorfailedattemptsatreplication. These reevaluations completely undermined the initial conclusions, which often had relied onmisguided statistical tests. Biologists were generally aware of these developments, though the follow-up studies received little attention in popular media.

There are indeed individual gene mutations that cause devastating disorders, such asHuntingtons disease. But most common debilitating diseases are not caused by a mutation of a single gene. This is because people who have a debilitating genetic disease, on average, do not survive long enough to have numerous healthy children. In other words, there is strong evolutionary pressure against such mutations. Huntingtons disease is an exception that endures because it typically does not produce symptoms until a patient is beyond their reproductive years. Although new mutations for many other disabling conditions occur by chance, they dont become frequent in the population.

Instead, most common debilitating diseases are caused by combinations of mutations in many genes, each having a very small effect. They interact with one another and with environmental factors, modifying the production of proteins from genes. The many kinds of microbes that live within the human body can play a role, too.

A silver bullet genetic fix is still elusive for most diseases. (Credit: drpnncpptak/Shutterstock)

Since common serious diseases are rarely caused by single-gene mutations, they cannot be cured by replacing the mutated gene with a normal copy, the premise for gene therapy.Gene therapyhas gradually progressed in research along a very bumpy path, which has included accidentally causingleukemiaandat least one death, but doctors recently have been successful treatingsome rare diseasesin which a single-gene mutation has had a large effect. Gene therapy for rare single-gene disorders is likely to succeed, but must be tailored to each individual condition. The enormous cost and the relatively small number of patients who can be helped by such a treatment may create insurmountable financial barriers in these cases. For many diseases, gene therapy may never be useful.

The Human Genome Project has had an enormous impact on almost every field of biological research, by spurring technical advances that facilitate fast, precise and relatively inexpensive sequencing and manipulation of DNA. But these advances in research methods have not led to dramatic improvements in treatment of common debilitating diseases.

Although you cannot bring your genome card to your next doctors appointment, perhaps you can bring a more nuanced understanding of the relationship between genes and disease. A more accurate understanding of disease causation may insulate patients against unrealistic stories and false promises.

This article is republished from The Conversation under a Creative Commons license. Read the original article. This opinions expressed in this article belong solely to the author.

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Genetic Testing Market size, leaders, segment analysis and forecast to 2030 interpreted by a new report – WhaTech Technology and Markets News

February 13th, 2020 12:49 pm

Genetic testing market is projected to grow considerably in the coming years by P&S Intelligence. The global genetic testing market size is projected to grow considerably in the coming years.

The global genetic testing market size is projected to grow considerably in the coming years, due to the growing number of test to study multiple genes that may help in managing individual health condition. Additionally, the government initiatives to spread awareness with respect to the advantages of procedure is further expected to drive the growth of the market.

The different technologies used for genetic testing include cytogenetic testing, molecular testing, and biochemical testing. Molecular testing was the most widely utilized technology used for testing and analysis of genes, and held the largest share in the global market, in 2016.

This leading position of the category is mainly attributable to the increasing analysis on the biological markers in the genome and proteome studies.

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Increasing application of the gene testing in oncological research, rising incidences of genetic disorders, technological advancements and rising demand for personalized medicine are the major drivers augmenting the growth of the genetic testing industry.

According to the WHO, sickle cell anemia is one of the genetic disordersparticularly common among people whose ancestors come from Sub-Saharan Africa, South America, Cuba, Central America, Saudi Arabia, India, and Mediterranean countries such as Turkey, Greece, and Italy.However, high cost involves in gene testing, and lack of the experienced professionals are the key factors hampering the growth of the genetic testing market.

Genetic tests in conjugation with other genomic technologies would help predict the risk of an individual to a disease and is also expected to assist clinicians to select suitable therapeutic interventions.

These factors also increase the opportunities for players in pharmaceutical industry to grow, by providing treatment options to their end users. For instance, 23andMe offers direct genetic makeup tests to the consumers and based on the results of tests, the company recommends genetic counsellors to help the consumers about the better testing of genes, and the inherited diseases.

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Astonishing growth in Precision Medicine Software Market is expected to grow at CAGR 12.3% from 2019 to 2027 – Instant Tech News

February 13th, 2020 12:49 pm

Some of the prominent players operating in the precision medicine software market include 2bPrecise, Syapse, Inc., IBM Corporation

Precision medicine is a prototype in healthcare which provides the customization of healthcare with medical decisions, practices, treatments, and products for patients in person. It states about right therapeutic approach for the right patient at the right time. The use of precision medicine is to identify which treatment approach is effective for patients on the basis of genetic, environment, and lifestyle factors. Precision medicine software allows the healthcare professionals (HCPs) to provide personalized treatment plans to patients based on their genetic content. It gives a wide range of applications in both the clinical and diagnostic areas and it combines genetic and clinical data to cater targeted patient care, which is increasing the demand of precision medicine software market.

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The global precision medicine software market is experiencing lucrative growth owing to the increase in the number of patients suffering from chronic diseases such as cancer, heart diseases, and diabetes. For instance, as per the data presented by International Agency for Research on Cancer (IARC), in 2018, the cancer burden was 18.1 million new cases and 9.6 million deaths across the world. One in five men and one in six women around the globe develop cancer during their lifetime, and one in eight men and one in 11 women die from the disease.

Koninklijke Philips N.V. (Philips Healthcare), a multinational electronics company focusing on healthcare, offers precision medicine platform, namely, IntelliSpace. It enables end-to-end oncology care or cancer management. The platform unifies and streamlines oncology care throughout the patient journey from molecular diagnostics to therapy recommendations. IntelliSpace, a precision medicine oncology solution integrates information over different clinical domains such as pathology, electronic health record (EHR) systems, radiology, and genomics. It consolidates all key patient and medical data in one location to represent a clear, comprehensible view of patient status in its disease and enable data driven clinical decision support, which in turn is propelling the precision medicine software market.

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Precision medicine with the integration of artificial intelligence (AI) will go to the next level with more accuracy and prediction of outcome for patients. Its major benefit for precision medicine is that it predicts outcomes as well as enables healthcare professionals to predict patients probability of having diseases in the future, thus driving the demand of precision medicine software market. Oracle, an American multinational computer technology corporation offers precision medicine software that enables researchers, clinicians, and molecular pathologists to work together. The software addresses data aggregation, normalization and workflow issues, knowledge exchange which restricts timely creation of patient molecular profiles and it also enables spectrum testing from gene panels through whole genome sequencing, and integration with electronic health record systems for seamless clinical workflow.

The detailed research study provides qualitative and quantitative analysis of the global precision medicine software market. The precision medicine software market has been analyzed from demand as well as supply side. The demand side analysis covers market revenue across regions and further across all the major countries. The supply side analysis covers the major market players and their regional and global presence and strategies. The geographical analysis done emphasizes on each of the major countries across North America, Europe, Asia Pacific, Middle East & Africa and Latin America.

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The Right Not to Know and the Obligation to Know – Practical Ethics

February 13th, 2020 12:49 pm

By Ben Davies

Most people accept that patients have a strong claim (perhaps with some exceptions) to be told information that is relevant to their health and medical care. Patients have a Right to Know. More controversial is the claim that this control goes the other way, too. Some people claim, and others deny, that patients also have a Right Not to Know.

A number of considerations (harm to the patient; autonomy; privacy) have been marshalled on either side of this debate over the past few decades (e.g. Laurie 2004; Robertson and Savulescu 2001; Herring and Foster 2012; Takala 2019). In this post, I focus on a distinct argument and its apparently unassailable logic. This is the view that a comprehensive Right Not to Know cannot be justified because in many cases a patients ignorance will likely lead harm to third parties (Council of Europe 1997; Rhodes 1998; Harris and Keywood 2001).

The logic of this argument is best put by Rhodes, who focuses on our rights and obligations with respect to genetic knowledge (though the priniple applies more widely). As she presents it, the lack of a Right Not to Know follows from the logic of a right, since To have a right is to have a freedom to do or not do, while to have a duty is to have no moral freedom. If you have an obligation to acquire certain medical information about yourself (as you do if your ignorance would harm others), you thus lack the moral freedom not to acquire that information. And that is, in Rhodess thinking, logically equivalent to lacking a right not to have that information.

This argument, superficially persuasive though it might be, faces two problems. Firstly, it is not true that the philosophers understanding of rights and duties as Rhodes puts it is as she suggests. Although she acknowledges as much in a footnote, her central argument ignores a further category of rights that exist in the canonical analysis by Hohfeld (1919). As well as understanding rights as liberties (i.e. absences of duties), Hohfeld suggests that we can understand them in several other ways, including as claims. Briefly, if A holds a claim-right against B, that means that B has a duty to A to do or not do something nothing is said about As duties (Wenar 2015).

The second issue is that in introducing this distinction, we can locate rights at different levels. Assume it is true that in some situations, a patient has an obligation to learn as much as possible about his health because of the potential impact on others. In this case it is true that he has a duty and hence no freedom at what we might call the moral level. Yet we might think that even in such cases, it is important that patients retain strong institutional protections against medical professionals, including a control over access to information about themselves. This would be a claim that patients have against medical professionals, justified at the institutional level of health care.

There is no paradox here. A patient can have a claim against, say, his doctor that she not give him information even if he has a duty (held towards separate individuals, such as relatives) to seek out that information. The compatibility of these two claims, and thus the failure of the argument from a duty to others, is obscured by ambiguity in the phrase, a Right Not to Know.

References

Council of Europe. 1997. Convention for the protection of human rights and dignity of the human being with regard to the application of biology and medicine: Convention on human rights and biomedicine. European Treaty Series 164

J. Harris and K. Keywood. 2001. Ignorance, information and autonomy. Theoretical Medicine 22: 415-36.

J. Herring and C. Foster. 2012. Please dont tell me: The right not to know. Cambridge Quarterly of Healthcare Ethics 21: 20-29

W. Hohfeld. 1919.Fundamental Legal Conceptions, W. Cook (ed.). New Haven: Yale University Press.

G. Laurie. 2004. Recognizing the right not to know: Conceptual, professional, and legal implications. Journal of Law, Medicine and Ethics 42: 53-63.

R. Rhodes. 1998. Genetic links, family ties, and social bonds: Rights and responsibilities in the face of genetic knowledge. Journal of Medicine and Philosophy 23: 10-30.

S. Robertson and J. Savulescu. 2001. Is there a case in favour of predictive genetic testing in young children? Bioethics 15: 26-49

T. Takala. 2019. Genetic moralism and health. Cambridge Quarterly of Healthcare Ethics 28: 225-235

L. Wenar. Rights.The Stanford Encyclopedia of Philosophy

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Five faculty members recognized with UBC Faculty Research Awards – UBC Faculty of Medicine – UBC Faculty of Medicine

February 13th, 2020 12:49 pm

Five members from the UBC Faculty of Medicine have been recognized with 2019 UBC faculty research awards for demonstrating excellence in research. Recipients include:

UBC Killam Research Fellowships

The fellowship enables faculty to pursue full-time research during a recognized study leave.

Nick Bansback, School of Population and Public Health

Dr. Bansback will be working on a digital health project based at the University of Manchester, UK where patients have been daily reporting their pain intensity in a large smartphone study. He will seek to help understand how this data can help patients make decisions about their daily activities using individualized predictions of future pain trajectories.

Miriam Spering, Department of Ophthalmology and Visual Sciences

Dr. Sperings research will focus on how people form memory representations since human memory is an important cognitive function that allows us to perceive, recognize, and keep track of objects and events around us. She will be using human eye movements as a window into sensory and cognitive processing with the ultimate aim to develop novel screening tools for sensory and cognitive dysfunction.

Lara Boyd, Department of Physical Therapy

Dr. Boyd will spend her study leave at the Florey Institute in Melbourne, Australia to gain advanced knowledge in the use of machine learning. This will enable her to apply algorithms to the datasets being generated in her lab in order to decipher new relationships among biomarkers and outcomes after stroke.

UBC Killam Research Prize

This research prize recognizes faculty for their outstanding research and scholarly contributions.

Andrew Krahn, Division of Cardiology, Department of Medicine

Dr. Krahn has published 416 papers in peer-reviewed journals such as Circulation, JAMA, Journal of the American College of Cardiology, the New England Journal of Medicine, and the European Heart Journal. His current research interests include investigation of genetic causes of arrhythmias, sudden cardiac arrest, syncope, and implantable arrhythmia devices. He has research funded by the Canadian Institute of Health Research through to 2027.

Presidents Award for Public Education Through Media

This award recognizes a faculty member who has demonstrated outstanding service to the University and the community by sharing research expertise via the news media.

Lori Brotto, Department of Obstetrics & Gynaecology

Dr. Brotto is a world-leading expert on sexual desire and arousal disorder. She has worked with Canadian and international news media to disseminate sexual health research and clinical advice.

Her achievements in actively and creatively sharing her research expertise through the media are exceptional examples of knowledge translation. Dr. Brottos media engagements include national network documentaries (Discovery Channels The Science of Lust and the CBCs The Truth About Female Desire), The New York Times Magazine, Women Who Want to Want, and as a guest columnist for the Globe and Mails health Advisor column.

Dr. Brottos engagement with the media has helped to break down the taboos surrounding female sexuality through the sharing of her own and others scholarly research and clinical experience. She has immensely contributed to public awareness of an important, yet neglected, topic. Her knowledge translation, extending far beyond individuals in her clinical practice, has helped untold numbers of women and their partners discover fulfillment in their relationships and inner lives.

Recipients were selected by UBCs Faculty Research Awards Committee, which includes arts and humanities, business, applied science, science, and medicine.

Each spring, the Office of the Vice-President Research & Innovation hosts an awards reception to recognize outstanding UBC researchers. This year the reception will be held on April 15, 2020 at the Jack Poole Hall of the Robert H. Lee Alumni Centre.

For a list of all Faculty Research Award recipients, visit UBC Research + Innovation.

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The genomic jigsaw of cancer – Pursuit

February 13th, 2020 12:49 pm

Imagine ten jigsaw puzzles, each with 150 million pieces, jumbled together in a huge box.

The jigsaws are all double-sided, with a different picture on each side. The images on them are bland and one in 100 pieces has the wrong picture.

Despite all of this, you have just two days to complete the puzzles.

Tricky enough for you?

This is essentially what scientists face figuratively speaking each time they sequence a human genome. When they do solve the puzzle, just four of the pieces hold the key information they need.

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It is an incredibly difficult and precise science, but mapping the human genome is revolutionising medicine, and researchers hope that it will help them to turn cancer into a manageable chronic disease like diabetes.

Until relatively recently, this sort of thing was a pipe dream.

The game changed significantly, however, when scientists announced that they had mapped the human genome in 2003. Since then, many others around the world have explored ways to use this ground-breaking information.

The potential for using an individuals genetic information to personalise their medical treatment is enormous. But what exactly is the human genome and how do you sequence it?

The genome is an organisms entire chemical blueprint. It is held as DNA in all cells with a nucleus and scientists are increasingly focusing on sequencing, or reading, genomes to understand the genetic functioning and causes of disease.

The human genome contains about three billion base chemical pairs, making it extremely difficult to read accurately. But that hasnt stopped University of Melbourne researchers from using the technology to help cancer patients and those at risk of developing it.

The information is already being used to better understand why a person is at risk or to pinpoint how each patient should be treated. Well-targeted treatments increase the chances of success and reduce the chances of failure and/or debilitating side effects.

Professor Sean Grimmond, the Bertalli Chair in Cancer Medicine at the University of Melbournes Centre for Cancer Research (UMCCR), is focusing on rare and challenging cancers, such as pancreatic cancer.

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People with pancreatic cancer have a five-year survival rate of less than 10 per cent.

The UMCCR is focusing on cancers of unmet need. These are the most challenging to treat cases, including rare or aggressive tumours, those resistant to standard therapies, or those that are traditionally difficult to diagnose.

When Professor Grimmonds team sequenced the genome of its first Australian cancer patient nine years ago, it took more than six months and cost about $A1 million.

Using new NovaSeq 6000 machines and the latest computer technology, it now costs the same as an MRI scan.

The science is cutting edge, but if youre picturing space-age shiny metals, rows of glowing buttons or laser lights then think again.

The Illumina NovaSeq machines that could save many lives resemble large, sleek photocopiers, with cartridges of reagents instead of ink to facilitate the sequencing process.

They live in the Victorian Comprehensive Cancer Centre, a building bringing together those at the forefront of world cancer research and treatment. Operated by the UMCCR, each machine has the capacity to sequence 50 human genomes in less than two days.

So, how do they do it?

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Sequencing a cancer patients genome essentially produces a genetic blueprint of their tumour. Initially, scientists take a tiny sample of the cancer, extract the DNA and process it before compressing it onto a slide.

The slide is fed into the sequencing machine, which produces terabytes of data that can only be decoded in pieces that are up to 150 bits long.

Scientists take those pieces and smash them into random bits to create a complex map that can be decoded. Hence, the jigsaw analogy.

Before you start, you draw lines between the pieces and come back to use those clues, Professor Grimmond explains. Its computationally very difficult. We can think of those bits as a computer hard drive your DNA is like a three-gig hard drive.

As well as mapping individual genomes, Professor Grimmond wants to build up enough combined data to establish patterns that will further advance treatment. Drug trials could also be personalised by pinpointing which trial drug a patient is better suited to.

Over the next three years, more than 1,000 Victorians with rare and challenging cancers are set to benefit from genomic testing through an initiative led by Professor Grimmond.

The Cancer of Unmet Need Initiative is piloting real-time testing of our most challenging cancer cases, integrating patients genomic data into routine clinical decision-making for a truly personalised approach to treatment and care, Professor Grimmond says.

The $A6 million initiative is the first flagship project of a partnership announced in 2019 by University of Melbourne and Illumina, one of the worlds leading biotech companies.

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While the overall outlook for people with cancer has almost doubled in recent decades, this initiative is targets those classes of cancers that have not seen these improved outcomes.

Its providing these patients with rapid diagnositics and a gateway to better cancer care and targeted clinical trials.

Professor Grimmond and his team are already sequencing patients as part of the Victorian Comprehensive Cancer Centres (VCCC) Precision Oncology program.

The ultimate goal is for precision oncology to turn cancer into a manageable chronic disease, as well as minimising treatment failure and side effects.

For example, if a drug has an 80 per cent success rate but sequencing suggested you were one of the 20 per cent of patients that it would not work on, your doctor could direct you to another more suitable treatment.

We want to take the guesswork out of therapy, Professor Grimmond says.

Ultimately, we want to help those at the forgotten fringes of cancer care on an individual level, to improve equity of patient outcomes.

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Lutein mkt projected to be valued at $454.8 mn by ’26, growing at 6.4% | FNB News – fnbnews.com

February 13th, 2020 12:48 pm

The global lutein market was calculated to be worth $274.6 million in the year 2018, and is projected to be valued at $454.8 million by the year 2026, delivering a CAGR of 6.4 per cent in that duration.

The rising incidences of cataract and age-related macular degeneration (AMD) have influenced the demand for lutein.

The fact that lutein is beneficial for the eyes and can protect and maintain healthy cells in the eyes, especially with our ever-increasing exposure to blue light, has led to the increased adoption of lutein supplements, and will subsequently bring to light more growth opportunities.

Lutein, an antioxidant carotenoid, is one of the two essential carotenoids that act as colour pigments in the human eye, and also gives the yellow colour to fruits and vegetables. In the eye, it acts as a light filter and prevents the eye tissues against damages caused by sunlight.

This article has been designed to encompass all vital aspects of the lutein industry that influence the growth of the sector. The companies functioning in the sector are undertaking strategic initiatives to gain a competitive advantage against all rival companies.

The major companies operating in the industry are Allied Biotech, BASF, Chr. Hansen, Dhler, DDW The Color House, E I D Parry, Fenchem, Lycored, PIVEG, and Zhejiang Medicine.

Back in 2015, DSM and Kemin had extended their partnership, launching FloraGlo Lutein, an eye health solution suitable for effective eye health ingredients.

In September 2019, the US-based company EyePromise debuted Screen Shield Pro as the latest addition to its eye vitamin range.

The product has been created with lutein and naturally-derived zeaxanthin to help prevent the eyes from damage caused by screens.

Based on form, lutein is mainly available in the forms of powder and crystalline, oil suspension, beadlet, and emulsion, whereas based on source, lutein is derived from natural as well as synthetic sources, and have major applications in the food and beverages sector.

Based on source, natural lutein is estimated to achieve a sizable growth due to the health benefits it offers.

However, synthetic lutein will dominate the market as it is easy to manufacture and are cost comparatively less than natural lutein.

The integration of lutein into dietary supplements will account for 27.4 per cent of the global market share.

Lutein has found extensive usage in eye care supplements and can also effectively prevent breast cancer, colon cancer, type 2 diabetes, and heart diseases.

The market extends to five major regions across the globe, viz., North America, Europe, Asia Pacific, Latin America, and the Middle-East and Africa.

Reports and Data estimates that the lutein market in the North American region will control the biggest portion of the global industry, and the Asia Pacific market will register the highest growth rate of 8.2 per cent in the forecast duration between 2020 and 2026.

The rising incidences of cataract and AMD in the region will drive the demand for the product in the region.

Data from the American Academy of Opthalmology indicates that nearly 24.4 million Americans aged 40 and older are affected by cataract, while almost 2.1 million Americans over 50 have late AMD, which leads to severe vision impairment.

Overall, the global lutein market exhibits tremendous growth potential for this decade, primarily originating from the increasing awareness among the population regarding the numerous health benefits of consuming lutein.

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Stem Cell Treatments Market to Exhibit Impressive Growth of CAGR during the per – News by aeresearch

February 13th, 2020 12:48 pm

Latest Research Report on Stem Cell Treatments Market size | Industry Segment by Applications (Nerve Diseases, Immunological Diseases, Musculoskeletal Disorders, Cardiovascular Diseases, Gastrointestinal Diseases and Other), by Type (Adipose Tissue-Derived Mesenchymal Stem Cells, Bone Marrow-Derived Mesenchymal Stem Cells, Cord Blood/Embryonic Stem Cells and Other Cell Sources), Regional Outlook, Market Demand, Latest Trends, Stem Cell Treatments Industry Growth, Share & Revenue by Manufacturers, Company Profiles, Forecasts 2025.Analyzes current market size and upcoming 5 years growth of this industry.

New research report to its expanding repository. The research report, titled Stem Cell Treatments Market, mainly includes a detailed segmentation of this sector, which is expected to generate massive returns by the end of the forecast period, thus showing an appreciable rate of growth over the coming years on an annual basis. The research study also looks specifically at the need for Stem Cell Treatments Market.

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The study includes the profiles of key players in the Stem Cell Treatments market with a significant global and/or regional presence. The Stem Cell Treatments market competition by Top Manufacturers Covers:

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The report contains the profiles of various prominent players in the Global Stem Cell Treatments Market. Different strategies implemented by these vendors have been analyzed and studied to gain a competitive edge, create unique product portfolios and increase their market share. The study also sheds light on major global industry vendors. Such essential vendors consist of both new and well-known players. Besides, the business report contains important data relating to the launch of new products on the market, specific licenses, domestic scenarios and the strategies of the organization implemented on the market.

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What is liposuction? How the procedure works and how painful it is – Insider – INSIDER

February 13th, 2020 12:46 pm

Getting liposuction from a practitioner who is board-certified in these types of procedures is safest. andriano.cz/Shutterstock

Liposuction is a surgical procedure to remove extra fat from your body. It started in the 1980s and has become one of the most popular plastic surgeries in the US. An estimated 258,000 Americans got it in 2018.

Today, you can expect to pay around $3,500 for liposuction and most health insurance plans won't cover the cost. But if you're willing to pay the price, liposuction is a relatively safe and quick procedure that can help you shed fat that diet and exercise can't.

Here's what you need to know about how liposuction works and why it's not a weight-loss tool.

Liposuction is a 1-to2-hour-long procedure where fat cells are permanently removed from your body, usually for cosmetic reasons. People who get liposuction don't do it to lose large amounts of weight but rather to help sculpt the shape of their body.

Some of the most common places to have fat removed are the belly, thighs, buttocks, arms, back, the upper neck just under the chin, and jawline/jowls.

Depending on where you're getting the procedure, doctors will either provide a local anesthetic to numb the area of operation or they will give you a general anesthetic so you're unconscious during the procedure.

Then, surgeons will often inject into the area of operation a solution containing a mix of saline solution, a numbing medicine, and medicine the decreases bleeding. This is to help the skin and fat separate from important structures like muscles and blood vessels so they aren't damaged during the suctioning process.

After that, the surgeon inserts a long metal instrument called a cannula under your skin. The cannula then vacuums out your fat. During this process, surgeons may also use a smaller microcannula to remove fat in nearby areas to achieve a more natural, smoother contour.

Once the fat is removed through liposuction it can be discarded or it can be injected back into your body to enhance features like breasts, buttocks, or face. Or, more recently, in the last decade or so, liposuction has also been used to retrieve stem cells a type of cell that can form other specialized cells in the body for laboratory research.

After liposuction, your surgeon will likely recommend you wear a temporary band or brace over the area of operation to help the skin heal. The band or brace also helps prevent fluid from building up in the area of operation where the fat was removed, between the skin and deeper structures like muscles and blood vessels.

Whether you are awake or asleep during liposuction, you shouldn't feel any pain during the procedure, says Marco A. Pelosi II, MD, a cosmetic surgeon with experience performing liposuction procedures. The recovery, also, should be a relatively mild process.

After getting liposuction, you will feel soreness similar to a muscle ache. "The level of this soreness is typically a 2 or 3 out of 10 for a few weeks," says Pelosi, adding that you should be able to go back to work in 2 to 3 days.

Ongoing pain near the area where the cannula was inserted is a risk of liposuction, and if the pain grows or pain killers don't help, you should tell your surgeon.

According to the Cleveland Clinic, you should not use liposuction as a weight loss alternative. It recommends that if you want to lose weight, you should first try diet and exercise, then use liposuction to take care of more stubborn areas like the chin or belly fat.

Moreover, research shows that people who keep up other weight loss practices like a healthy diet and exercise will see better results after liposuction and keep fat from returning to a particular area.

This is because while liposuction permanently removes fat cells from your body, there is nothing to stop the remaining fat cells from getting bigger if you gain more weight.

There are some important safety tips to look for when choosing a liposuction provider.

First, look for a facility that meets national safety requirements. You can verify if a facility is accredited on the American Society of Plastic Surgeons' website here.

Pelosi says that doctors should also do blood work testing and medical clearances before a liposuction procedure to ensure your safety. These tests are to make sure you can safely undergo general anesthesia without complication. If, for example, you have an infection or are pregnant, you may not qualify for the surgery.

Last, but not least, is to look for a surgeon who is board-certified in performing these types of procedures and also has extensive experience with liposuction procedures so you know that they are well versed in the technique. To find out more about a practitioner's experience with liposuction, you can check the American Society of Plastic Surgeons' website.

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Penn State receives grant to study bioprinting tissue for facial reconstructions – The Daily Collegian Online

February 13th, 2020 12:46 pm

Penn State researchers have received a $2.8 million grant to investigate 3D bioprinting tissue for facial reconstructions, according to a Penn State news release.

The grant, from the National Institutes of Healths National Institute of Dental and Craniofacial Research, funds five years of research exploring methods for bioprinting face, mouth and skull tissue directly into patients during surgery, with the ultimate goal of developing a bioprinting technology, according to the release.

Craniomaxillofacial reconstruction currently presents challenges for doctors because it requires precisely stacking several different types of tissue. Penn States researchers hope to solve this problem by bioprinting the tissue directly into the subject, according to the release. Researchers will also be investigating the use of stem cells, biomaterials and differentiation factors in this process.

The team of researchers that received the grant includes professors of plastic surgery, biomedical engineering, and orthopedics and rehabilitation.

The researchers plan to investigate printing each type of tissue necessary for craniomaxillofacial reconstruction bone, fat and skin tissue individually, then study composite tissues that include all three of these layers. They hope that this will help them better understand how vascularization occurs in each type of tissue.

Ultimately, researchers hope to learn how different types of tissue interact and how bioprinting tissue directly into subjects will affect the facial reconstruction process.

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Cell-based meat in focus: In conversation with Meatable, Finless Foods, New Age Meats – FoodNavigator-USA.com

February 13th, 2020 12:46 pm

Despite all the hype, most startups in the space are still working in a laboratory (as opposed to a factory), although several have recently raised more substantial sums (Memphis Meats: $161m, Future Meat Technologies: $14m, Wild Type: $12.5m, Aleph Farms: $12m, Meatable: $10m) to support the construction of pilot-scale facilities.

Maastricht-based Mosa Meat which is gearing up for a small scale commercial launch in 2022 assuming it has cleared regulatory hurdles - recently joined forces with Nutreco (which has invested an undisclosed sum in the firm along with Lower Carbon Capital) to work on growth media; San Diego-based BlueNalu has also partnered with Nutreco; while Jerusalem-basedFuture Meat Technologies plans to release hybrid products in 2021 and a second line of 100% cell-based ground meat products suitable for burgers and nuggets at a cost of less than $10 per pound in 2022.

However, the recent $161m investment in Memphis Meats - which says it has a pretty clear path to achieving cost parity with conventional meat has given the whole sector a confidence boost, says Krijn de Nood, CEO at Dutch cell-based meat startup Meatable.

Its a huge positive for the industry, it shows there are very serious investors that have done their due diligence and think this is really going to happen.

Meatable - which is working with porcine and bovine induced pluripotent stem cells [iPSCs] recently raised $10m from existing investors and a couple of new angel investors, and a grant from the European Commission, which we are pretty proud of, says de Nood.

While this is dwarfed by Memphis Meats latest round, it was a meaningful vote of confidence in a sector where most startups have not raised more than a couple of million, he says.

Defendibility is definitely important to investors and we have IP around the differentiation of the cells, the hardware we use to grow the meat in, on reducing the costs on a lot of components. We have one patent thats granted, and a couple of others in the making.

Were comfortable that by late summer we can present our first prototype product, a tenderloin. Were aiming to present a product that has a meat-like texture with fat and muscle, with edible scaffolding, although I cannot disclose the materials at this point.

In the beginning of 2022 we should have a small pilot facility online, enabling some consumers to get familiar with our product. By 2025, we hope to have an industry scale facility online when we can become more cost competitive with traditional meat.

He adds:Weve worked on stabilizing the cell lines, culturing them in suspension and optimizing the proliferation speed.

Our cells can grow in an FBS-free [fetal bovine serum-free]medium and weve made good progress on reducing dependency on expensive growth factors.

As for market entry, Meatable is currently building a dossier to make a Novel Food application [to access the EU market], but also exploring the potential of market entry in Singapore, he says.

Cell-based fish co Finless Foods, which has a team of 11 people in Emeryville California, raised $3.5m in 2018, but is now gearing up to raise a series A round, says CEO Mike Selden.

While the startup co-founded by Selden and Brian Wyrwas, molecular biologists who met at theUniversity of Massachusetts, Amherst has experimented with multiple species, they have focused on Bluefin tuna because its under threat (populations today are a fraction of what they were in the 1960s) and because its expensive (reaching price parity with a broiler chicken could take far longer).

Investors are looking for a unique IP angle, as well as well-rounded teams and proof youre doing regulatory the right way and not just moving fast and breaking things, says Selden.

Now were gearing up for a Series A, we think there are some interesting things we can file [patent]and not have stolen from us, but were never going to file our media formulation [which would remain a trade secret].

As to how Finless stacks up vs the competition, he says, I wont pretend to know exactly what all of the others are doing; there are something like 40 cell-based meat companies and six cell-based seafood companies that Im aware have been funded. But I do think were not only competitive but actually I think youll see in the next few months at the forefront, as we release more information about what weve been working on.

Were the tuna people, so it will be very difficult to work on tuna outside of Finless Foods, plus we can take varieties of seafood that Americans have no real access to and localize them to the American market; things that are only eaten in Japan because no ones figured out how to farm, or theyre only available in small quantities in the wild.

Right now, Finless is focused on muscle and fat cells, says Selden. Its easy to have the muscle and fat cells turn into connective tissue, so we dont need a separate culture for fibroblasts.

As for getting the cells to proliferate indefinitely (so you dont keep having to go back to the source), he says, The concept of immortalization isnt super-relevant for seafood; fish cells naturally have an extremely high amount of telomerase [an enzyme which helps prevent the shortening of the telomeres, repetitive DNA sequences at the ends of chromosomes].

Put more simply, every time cells divide, their telomeres shorten, which eventually prompts them to stop dividing and die, he explains. Telomerase prevents this decline in some kinds of cells by lengthening telomeres, which is why people interested in slowing cellular aging are so interested in it.

It basically means we dont have to do genetic engineering to immortalize the cells.

As for the growth medium that feeds the cells, he notes, We currently have multiple cell lines and bluefin populations that are growing out in completely serum-free media, no FBS, no FCS (fetal calf serum). The key ingredients are salts, sugars and proteins. Right now, were getting these proteins from recombinant microbial systems [ie. expressing proteins in microbes such as bacteria, yeasts and other hosts].

There is some research thats happening both inside of Finless Foods and out, on what I consider to be better, more efficient ways of doing that, but I wont pretend that its come to fruition yet at least internally, but I know that others have had success such as [Tokyo-based cell-based meat co]Integriculture, which has been able to use conditioned media [spent cell culture media that includes secreted factors that have accumulated in the medium over time, including growth factors] instead [of recombinant growth factors] to feed their cells.

At Finless Foods, he explained, Our costs have come down massively, but as were working on Bluefin tuna [a very expensive fish]we dont face quite the same challenges [as companies trying to make, say, cell-based chicken, beef or pork].

Asked about bioreactors, he says, Were creating different divisions of the company working on different types of bioreactors to see what scales up the best, but as of right now, weve had more success in single systems, where the proliferation happens in one bioreactor and instead of moving the cells to a different bioreactor for the differentiation phase, you basically just replace the media from growth media to differentiation media and leave the cells in the same tank.

As for different ways to culture cells in the growth/proliferation phase, he says, one division of the company is working on suspension culture, where the infrastructure is already in place; while the other is working on attachment culture [where cells attach to food grade materials], which has never been scaled up, but has the potential for higher efficiencies. In suspension we have some experiments where the cells are attached to beads and others where the cells are just free-floating.

Were also exploring both approaches [suspension and attachment] in the differentiation phase, but there isnt a scenario where the cells are proliferating in a single cell suspension, but then differentiating attached.

When it comes to creating more structured, steak-like products, its potentially easier to recreate the structure/texture of tuna, which is more like a gel, compared with something like beef steak, he notes.

The first wave of cell-based products is going to attract a premium, which makes launching at a small scale in high-end restaurants - a place where consumers may be more willing to try something novel - a good way to test the waters, he says.

We definitely face more regulatory and technical challenges than plant-based meat companies,but brands such as Impossible Foods and Beyond Meat have paved the way for us to some extent by getting consumers - but also chefs - open to the idea of eating meat without slaughtering animals. Theyve also made foodtech cool and sexy, so were really grateful for that.

Asked about terminology, which has proved a bone of contention in the nascent industry, he said:I like the term cell-based because its neutral and accurate. Yes, we know that everything is made of cells[including meat from slaughtered animals], but we think its the best term out there.

I dont really get the term cultivated meat[a term emerging from Mattson/GFI research last year],but if there was a ton of evidence to support it, or if stakeholders in the animal ag industry were all behind it, I could be convinced, as Im not super ideological about this.

But the North American Meat Institute has signed off on cell-based and the government seems pretty OK with using it [editor's note: USDA and FDA have yet to issue any formal declaration on terminology].

At fellow startup New Age Meats,which has just raised $2.7m in a round led by ff Venture Capital to fund its cell-based pork operation, founder Brian Spears says investors are looking for clear evidence that yields are going up, and costs are going down.

While investors understand that cell-based meat is a longer-term bet than plant-based meat, and fits more into the high risk, high reward category given its novelty, the total addressable market for both is clearly enormous provided the products are good and the price is right says Spears, a chemical engineer with a background in industrial automation.

Were very focused on automation, data science and bioprocess, and showing that the cost of making cultivated meat is continuing to decrease. Weve got a high throughput platform that optimizes media, and weve validated different types of bioreactors, one of which was 200 liters, which I think is the biggest bioreactor that has been made specifically for cultivated meat.

While the nascency of the industry has meant most cell-based meat companies are vertically integrated, more third parties are now creating platforms to help cell-based meat startups, he says:

Weve seen a lot of players step in, so 3M has a whole team dedicated to optimizing media for cultivated meat, while Black & Veatch is interested in working with companies on industrial scale manufacturing.

New Age Meats is looking at pork belly, bacon, and sausages, some of which present greater technical challenges than others, says Spears.

In all cases, he says, [animal]fat is crucial, its where the flavor is, the mouthfeel, the smell. Just growing muscle and then adding a plant-based fat gives you a very different experience. Right now the most, straightforward solution if youre making a simple product like a sausage is to grow muscle and fat cells separately, and then combine them at the end, but there are pros and cons to each method.

Asked about more structured products such as pork belly, he said:There are a lot of ways to create a 3D structure; people think you have to make this edible scaffolding or matrix, flow the cells in, they adhere to it and they grow and mature on that, but there are other methods of doing this.

There are some processes New Age Meats could patent, but at this point, given the expense, its not top of the priority list, says Spears, who has adopted the term cultivated meat.

Patents give an easy signal to investors, but some of the patents in this space are absolutely worthless.

Read more here:
Cell-based meat in focus: In conversation with Meatable, Finless Foods, New Age Meats - FoodNavigator-USA.com

Read More...

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