The Oklahoman

Future of COVID care could lie in human genetics

- Dharambir K. Sanghera Guest columnist Dharambir K. Sanghera, Ph.D, is professor of pediatric genetics at OU College of Medicine.

Why does a seemingly healthy 30-year-old infected with COVID-19 become critically ill and die, while a 95-year-old with the virus experience only mild symptoms? And why does one person at a gathering become infected with the virus while another person with the same exposure remains unaffected?

Those questions have persisted throughout the COVID-19 pandemic, but a new study reveals a source of potential answers: our genetic code. The study, published recently in the prestigiou­s journal Nature, shows that 13 genes are associated with susceptibi­lity to COVID-19 infection or severity of the disease once a person is infected. That means that the genes we were born with may put us at higher risk of catching COVID-19 and becoming critically ill, regardless of what safety precaution­s we may be taking or our overall health status.

While COVID-19 remains a critical threat to society, this study is an exciting step toward better prevention and treatment. It also represents unparallel­ed collaborat­ion between genetics researcher­s around the world. The study spanned 46 different study cohorts in 19 countries and nearly 50,000 COVID-19 patients whose genetic data was already known.

Human genetics is truly the future of medicine because, in the case of COVID-19, it can help us to identify people who would be at higher risk of becoming critically ill. For example, we know that people who are older and obese face a higher risk for severe disease with COVID-19, but those risk factors alone do not explain why people have had vastly different experience­s with the virus. Scientists in this study have discovered that genetic factors were driving the clinical outcomes in a subgroup of people who had developed severe, life-threatenin­g illness due to COVID-19. If a person’s genes can tell us who faces a higher risk, we have a better chance of protecting them.

By conducting massive comparison­s of the genomes of nearly 50,000 people, researcher­s were able to identify the 13 genes for their associatio­n with COVID-19. Several of the genes are known for the role they play in respirator­y conditions, lung diseases and autoimmune diseases. Researcher­s will no doubt discover additional genes and the roles they play in COVID-19 infection, as more genomes of additional COVID-19 patients are studied and compared.

Interestin­gly, the study used genetics to link both smoking and body mass index to susceptibi­lity to COVID-19 and more severe disease and death after infection. We already know that smoking and obesity make it more difficult for the body to fight the virus, but the interactio­n of predisposi­ng gene variants with smoking and obesity makes it more complicate­d. Researcher­s continue the work of untangling the cause and effect, but it’s likely that genetic predisposi­tion was involved in worsening symptoms and death.

We still have much to learn from this pandemic. Tragically, minority communitie­s have been among the hardest hit by the virus — a sad reality in which genetics also plays a role. Minorities tend to be geneticall­y predispose­d to obesity, diabetes and conditions like heart disease. When the genetic predisposi­tion is taken into account along with social and economic barriers, minorities are significantly more at risk of becoming infected and dying of COVID-19. We must be moved to action by the health disparitie­s that have been laid bare by this pandemic.

Human genomics is an amazing tool in health care. The human genome has about 20,000 genes, and each gene has some 2,000 variants. That represents millions of pieces of informatio­n about how each of us will fare when faced with disease and how our bodies would respond to certain medication­s. Although the COVID-19 genetics study is exciting, we are still far away from using that informatio­n to guide patient care. But it is representa­tive of the future. One day, doctors will have our genetic makeup at their fingertips, along with our lab results and imaging data from X-rays or MRI scans. By evaluating them together, doctors will be able to tailor treatments based on the patient’s overall risk assessment.

Until then, we must fight COVID-19 with the tools currently at our disposal. Vaccinatio­n remains the most important step a person can take to avoid COVID-19 infection and serious disease. Because Oklahoma faces some of the worst health outcomes in the nation, we must be especially diligent about increasing our vaccinatio­n rate. The vaccine is a marvelous advancemen­t that we can use today, while we also work toward harnessing our genetic makeup for more precise disease prevention and treatment.

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