Even in the midst of the COVID-19 pandemic, the medical community made advances throughout 2020. Here are 5 of the years most impactful innovations.
Overall, 2020 has been a tumultuous year. From a health perspective, its been one turned upside down with a deadly global pandemic reorienting how we live our lives and relate to others.
The COVID-19 pandemic has justifiably dominated headlines and attention from media, policymakers, and health officials alike.
While its clearly the defining public health, cultural, economic even political event of the year, the pandemic shouldnt obscure the fact that 2020 was also a time of great medical innovation.
From breakthroughs in oncology, gene therapies, and heart health, to the development of COVID-19 vaccines that are now being administered domestically and around the world, theres a lot that the medical community can be proud of in 2020.
Healthline touched base with leading experts about some of the most impactful medical advances of the year and how they hint at a more hopeful tomorrow.
Almost every expert Healthline interviewed agreed that gene editing was one of the big stories of the year.
In October, Emmanuelle Charpentier and Jennifer A. Doudna were awarded the Nobel Prize in Chemistry for discovering the CRISPR/Cas9 genetic scissors. (Just five other women have won this prize before).
This gene scissor tool is what it sounds like enzymes snip out pieces of DNA to restore them to their normal function, Dr. William Morris, executive medical director of Cleveland Clinic Innovations, told Healthline.
Charpentier and Doudna showed that these genetic tools could be controlled to cut any kind of DNA molecule at a designated location not just distinguish DNA from viruses, as these scissors exist in their natural form.
Essentially, it means we can rewrite the code of life, according to the Nobel Prizes official announcement.
Morris said that this innovation has wide-ranging ramifications for people who have a wide range of genetic conditions.
He cited sickle cell disease, a condition where malformed sickle-shaped red blood cells cause blockages in blood flow, preventing the protein hemoglobin from effectively ferrying needed oxygen through the body.
Morris said these microscopic tools can cut out these genetic errors.
There have only been a handful of drugs to treat these kinds of conditions in the past.
Now, this kind of development allows you to remove the error and replace the [genetic] code, kind of like in your computer or your iPhone if you downloaded a patch for new software to repair an app that always crashes thats what this is, Morris explained.
Its so earth-shatteringly amazing to tell these patients who otherwise faced an entire lifetime of pain and suffering. You can now use the word cure, which is unbelievable to think about, he said.
Olivier Elemento, PhD, director of the Englander Institute for Precision Medicine at Weill Cornell Medicine in New York City, told Healthline that 2020 is the year of the genetic code.
Were really able to use the genetic code in humans and viruses to help humanity in ways we were not equipped to before, in ways we couldnt do before, Elemento said.
He added that gene therapy in general, along with this CRISPR technology, is pretty extraordinary.
This more comprehensive understanding of genetics extends beyond the Nobel Prize.
For instance, Elemento said Weill Cornell Medicine, where he currently works, along with New York-Presbyterian Hospital and Illumina Inc. recently announced an initiative to sequence the genome of thousands of patients.
The more we understand about genetics and gene therapies, the more improved our precision medicine capacity will be opening up the possibilities of creating targeted therapies for all kinds of conditions.
Recently, the American Heart Association released its own list of innovations in medical treatments.
The spotlight includes a new phase 3 study that could change the way hypertrophic cardiomyopathy (when the heart muscle thickens and can stiffen) is treated.
It also highlights new treatments that might change up the first-line treatment for atrial fibrillation (AFib) a new minimally invasive surgery to prevent stroke and a new trial that reveals more treatment might not necessarily mean better treatment for coronary heart disease.
American Heart Association President Dr. Mitchell S.V. Elkind, MS, FAAN, FAHA, wrote in an email to Healthline that all of these advances over the past year reflect connections between seemingly disparate areas of medicine and the fact that we are most successful when we break down the barriers between fields.
In order to tackle an issue as wide ranging as heart disease, for instance, it takes an interdisciplinary, comprehensive approach.
For example, we learned more this year about the unexpected ways in which medicines designed to treat diabetes, the sodium glucose transporter 2 inhibitors, or SGLT2 inhibitors, help patients with heart failure, even those without diabetes, he added.
Elkind also cited our growing understanding of how connections between infectious diseases like the flu and COVID-19 are tied to greater risk for heart disease and stroke.
Often, the most important advances occur when experts from different areas work together in creative ways to solve a difficult problem, he wrote.
When asked if there was one particular heart health innovation that stood out the most to him, Elkind said that what resonated with him was something not tied to fancy medications or groundbreaking research.
An analysis of people from across the U.S. showed that rates of blood pressure control have begun to decline in the U.S., after almost two decades of better control. High blood pressure is one of the most important and easily treated risk factors for stroke and heart disease, and so this backsliding is especially alarming, he added.
He stressed that the study also pointed to the impact that having health insurance has on controlling ones blood pressure.
Those with some form of health insurance had blood pressure control rates of 4354 percent, while for those without insurance, it was only 24 percent, Elkind explained.
Improving access to quality care is one of the best ways we have to improve health, and that is where we at the American Heart Association will be placing our efforts in the coming years, he said.
Benjamin Neel, MD, PhD, director of the Perlmutter Cancer Center at NYU Langone Health, said 2020 has been a year thats seen cancer research push forward on multiple fronts.
He said technologies are in development for early detection of cancer by way of blood tests.
Its been known for quite some time that tumors release DNA into the blood stream, we have technology developing from the standpoint of monitoring tumors, conducting sensitive tests for tumors, for tests for recurrence of cancers and protein-based tests, Neel told Healthline, outlining current research.
He also cited technology that modulates the regulatory DNA sequence patterns which refers to the part of the DNA molecule that can change the way a gene expresses itself in a living thing to pinpoint when methylation patterns might point to the development of cancer.
Among other research highlights over the past year, Neel said researchers have been developing new ways of drugging genetic mutations.
He mentioned work being done in developing a compound to degrade the androgen receptor for prostate cancer cells what allows these cancer cells to grow.
One of the biggest changes this year came in the form of how our new normal work-from-home lifestyle has impacted medicine.
As more and more people stay away from offices and public spaces, theyre turning to telemedicine. The Zoom screen is the new doctors office.
Morris said that, while this isnt a medical discovery per se, its a crucial in some ways life-saving development for how we relate to healthcare in our lives.
Out of this whole pandemic, one of the things weve discovered as clinicians is that we need to see patients where they are and not force them to cross state lines, Morris said. While we had telemedicine, we had some patients over Skype and video visits, there were clear disincentives and policies in place against people easily crossing state lines to seek medical care, of receiving care remotely.
He said the pandemic facilitated a push at the government level and with state and federal regulators to reduce barriers to these tools that are critical lifelines for patients.
Even when healthcare professionals couldnt always see patients in person this year, the embrace of telemedicine has resulted in unprecedented increases in the adoption and use of these tools and seeking care, Morris added.
This pandemic has challenged us to question old perceptions and policies, so that was a very positive thing, he stressed.
Innovation doesnt necessarily have to be an aha moment in a lab or something right in front of us, he said. Its unfortunate we needed a pandemic or a challenge to sometimes see a barrier, and sometimes that barrier is us.
This year, a possible breakthrough in Alzheimers disease research and treatment came in the form of a blood test that can diagnose this progressive form of dementia.
While the news is huge, the test is still in the trial phase.
If ultimately approved, a simple test for the condition would be a game changer.
There are as many as 5 million people living with Alzheimers in the United States, a number that will likely triple by 2060, according to the Centers for Disease Control and Prevention (CDC).
While this test has yet to go through all the proper approvals, a company distributed the first publicly available Alzheimers blood test this fall.
As 2020 comes to a close, experts are looking to a more hopeful new year.
For its part, Cleveland Clinic, which enters its centennial next year, released a list of the predicted top 10 innovations of 2021.
Morris said that while many think of this year as fraught and divisive full of tragedy and setbacks looking back at these innovations shows theres always something to be grateful for and look forward to.
Elemento said that he expects a biotech and pharma boom in the next few years.
Citing the breakthroughs in gene therapies and genetic manipulation indicate what will be a continual embrace of this kind of medical technology.
All these technologies, now everyone knows they exist and that they can be used for good, it will be a big boom for these technologies, Elemento added.
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5 Medical Innovations You Probably Didn't Notice Happened in 2020 - Healthline
- Krystal Biotech Inc (KRYS) Reports Strong Q4 and Full Year 2023 Financial Results - Yahoo Finance - February 27th, 2024
- New sickle cell gene therapies are a breakthrough, but solving how to pay their high prices is a struggle - CNBC - February 27th, 2024
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- Former Penn employee sues Gene Therapy Program director, alleging 'unethical and illegal conduct' - The Daily Pennsylvanian - February 27th, 2024
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- Fetal surgery expert Tippi MacKenzie shifts to in-utero gene therapy - STAT - February 27th, 2024
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- Ring Therapeutics, a Flagship gene therapy startup, lays off 20% of staff - STAT - February 27th, 2024
- Ed Silverman on new gene therapies, biosimilars, coffee, and more - STAT - STAT - February 27th, 2024
- Combatting HIV using gene therapy - Drug Target Review - February 27th, 2024
- NCDHHS working with federal government on increasing access to sickle cell disease treatment - WECT - February 27th, 2024
- Cell Therapy Weekly: FDA Approves First Cell Therapy For Solid Tumors - RegMedNet - February 27th, 2024
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- New sickle cell therapy uses gene editing at MUSC | Health | postandcourier.com - The Post and Courier - February 27th, 2024
- Long-term and real-world safety and efficacy of retroviral gene therapy for adenosine deaminase deficiency - Nature.com - February 18th, 2024
- Gene therapy, blood transfusions, stool monitoring: The Sydneysiders trying to escape death - Sydney Morning Herald - February 18th, 2024
- Not too late to repair: gene therapy improves advanced heart failure in animal model - Baylor College of Medicine | BCM - February 18th, 2024
- Direct Administration of CRISPR-Cas9: Tools for Cell and Gene Therapy - Forbes - February 18th, 2024
- Gene therapy's promise seen in its success for AADC deficiency - AADC News - February 18th, 2024
- First Patient Randomized in AskBio Phase II Gene Therapy Trial for Congestive Heart Failure Treatment - Diagnostic and Interventional Cardiology - February 18th, 2024
- FDA to review expanded use of Sarepta Duchenne gene therapy - Yahoo Finance - February 18th, 2024
- How gene therapy can help treat a rare blood disorder - KUTV 2News - February 18th, 2024
- CRISPR gene therapy Casgevy secures approval in Europe - Pharmaceutical Technology - February 18th, 2024
- FDA Updates for the Week of Feb. 12, 2024: New Approvals, an Extended Review and Goal Dates Set - Managed Healthcare Executive - February 18th, 2024
- First Patient Randomized in AskBio Phase II Gene Therapy Trial for Congestive Heart Failure - Business Wire - February 18th, 2024
- Lisa Jarvis: A cure for some kinds of hearing loss? Gene therapies are getting closer - St. Paul Pioneer Press - February 18th, 2024
- Spinal Muscular Atrophy Market: Navigating Therapeutic Advances towards USD 5.6 Billion by 2034, with a CAGR of ... - Yahoo Finance - February 18th, 2024
- Crispr Therapeutics' Gene Therapy Wins EU Approval - TipRanks.com - TipRanks - February 18th, 2024
- Revolutionizing Gene Therapy: A Novel Technique for In Vivo CAR T Cells - Medriva - February 18th, 2024
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- Gene Therapy: A Ray of Hope for Heart Failure Treatment | Health News - Medriva - February 18th, 2024
- Gene therapy trials restore hearing to children born deaf - The Hill - February 2nd, 2024
- Early Trial Success for Inherited Deafness Gene-Therapy - RegMedNet - February 2nd, 2024
- Sickle cell gene therapy first focus of Medicaid pay model - Modern Healthcare - February 2nd, 2024
- Beyond chemotherapy: Navigating the promise and perils of CAR-T therapy in pediatric cancer - BioPharma-Reporter.com - February 2nd, 2024
- Angiodema: Gene therapy blocks painful hereditary disorder - BBC - February 2nd, 2024
- FDA: Genome editing therapies may use accelerated approval pathway - Regulatory Focus - February 2nd, 2024
- CRISPR tech treats severe hereditary condition successfully - Interesting Engineering - February 2nd, 2024
- Gene Therapy Restores Hearing in Small Trial for Kids With Hereditary Deafness - Technology Networks - February 2nd, 2024
- Gene-based therapy may slow development of life-threatening heart condition - Medical Xpress - February 2nd, 2024
- Jaguar Gene Therapy Announces FDA Clearance of IND to Study JAG201 in a Genetic Form of Autism Spectrum ... - Business Wire - February 2nd, 2024
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- 2 Dutch among 10 "functionally cured" of hereditary swelling disease by new gene therapy - NL Times - February 2nd, 2024
- FDA publishes final industry guidance for CAR-T and gene therapies - PMLiVE - February 2nd, 2024
- Gene therapy cures hereditary deafness in two people - Advanced Science News - February 2nd, 2024
- Hearing Restored in Deaf Children in Gene Therapy Clinical Trial - Securities.io - February 2nd, 2024
- Vivet Therapeutics Receive 4.9 Million to Advance Development of Gene Therapy - European Pharmaceutical Manufacturer - February 2nd, 2024
- Adverum Biotechnologies will Host Webcast to Review LUNA Phase 2 Preliminary Efficacy and Safety Results on ... - GlobeNewswire - February 2nd, 2024
- Allogene parks Notch CARs, leaving one on the road - FierceBiotech - February 2nd, 2024
- Experimental gene therapy allows kids with inherited deafness to hear - The Associated Press - January 25th, 2024
- Gene-therapy breakthrough allows congenitally deaf children to hear Harvard Gazette - Harvard Gazette - January 25th, 2024
- Gene therapies restore hearing in several kids with inherited deafness - Livescience.com - January 25th, 2024
- Boy born deaf can hear for the first time thanks to a gene therapy procedure - NBC 6 South Florida - January 25th, 2024
- Gene therapy restores hearing in children with hereditary deafness - Medical Xpress - January 25th, 2024
- Children's Hospital of Philadelphia Performs First in U.S. Gene Therapy Procedure to Treat Genetic Hearing Loss - PR Newswire - January 25th, 2024
- Children's Hospital of Philadelphia uses gene therapy to help 11-year-old boy hear for 1st time - WPVI-TV - January 25th, 2024
- Breakthrough gene therapy treatment restores hearing in children born deaf - The Independent - January 25th, 2024
- Gene Therapy Administered Via Virus Cures Deafness in 11-Year-Old Boy - Futurism - January 25th, 2024
- 11-Year-Old Boy Hears For First Time Ever Thanks To Gene Therapy Breakthrough - IFLScience - January 25th, 2024
- Gene Therapy Deafness | National | caledonianrecord.com - The Caledonian-Record - January 25th, 2024
- Sickle cell gene therapy to be covered by Blue Cross insurers - Modern Healthcare - January 25th, 2024
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- Gene Therapy Deafness | Nation | The Daily News - Galveston County Daily News - January 25th, 2024
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- Gene therapy helps restore hearing in children with hereditary deafness - Shropshire Star - January 25th, 2024
- Gene therapy breakthrough enables deaf boy to hear for the first time - The Week - January 25th, 2024
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