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Genetics play role on effects of COVID

Virus affects all of us differentl­y, study finds

- Karen Weintraub

It is among the lingering mysteries of COVID-19: Why do some people catch it while others – sometimes even sleeping in the same bed – escape without symptoms?

Some factors have long been clear: Older adults are more likely to fall seriously ill, particular­ly if they smoke, are obese or have diabetes. People never exposed to the coronaviru­s won’t get sick, and exposure to a high concentrat­ion poses a higher risk for infection. The virus itself matters, too. The delta variant seems to be more contagious than earlier ones.

Even two people who look the same on paper can have a different reaction to COVID-19. Young, previously healthy people have died or been seriously disabled; 90-year-olds in cancer treatment have survived infection. The explanatio­n, a study published Thursday suggests, may lie in their genetics.

“The human genome, and not only the viral genome, matters,” Andrea Ganna, one of the lead authors of the study, said Wednesday at a news conference. “Clearly, there is a role of genetics in COVID severity … it’s one of the many risk factors.”

In younger people, less likely to have health problems that put them at higher risk, genetics may play an even bigger role, said Ganna, a group leader at the Finnish Institute for Molecular Medicine and an instructor at Harvard Medical School and Massachuse­tts General Hospital. The study, led by the COVID-19 Host Genomics Initiative, confirms or newly identifies 13 genes that appear to play a role in susceptibi­lity to infection or that affect the severity of illness. One gene is involved in the response to respirator­y infections. Others have no obvious explanatio­n. Blood type affects 9% to 12% of disease susceptibi­lity, but researcher­s said they could not explain why. Of two people with the same exposure to

the virus, the one with Type O blood will have slightly lower risk of getting infected. Yet blood type appeared to have no effect on severity of disease.

To be teased out is the cause and effect, said Dr. Michael Murray, a professor of genetics and director for Clinical Operations in the Center for Genomic Health at the Yale School of Medicine, who was not involved in the study. High body mass index might be a risk factor for COVID-19 because being severely overweight may make it harder to clear a virus, or the genetics contributi­ng to weight gain may be the same genes contributi­ng to more significan­t illness, he said.

These genetic effects have about as much influence on susceptibi­lity and seriousnes­s of infection as the effect of obesity or diabetes, said Benjamin Neale, a statistica­l geneticist at the Broad Institute of Harvard and MIT.

“DNA isn’t destiny but it can load the dice,” his colleague Hamdi Mbarek, director of the Qatar Genome Program, which participat­ed in the research, said via email. “This study is a big step towards understand­ing how many people may be playing with loaded dice when it comes to getting severely ill – or even having ‘long COVID’ – from the Delta variant, and future variants of the virus.”

The study involved 50,000 patients across 25 countries. “It’s really very important to conduct these studies on a worldwide level, because that increases our chance of making the broadest and most general discoverie­s,” said Mark Daly, another lead author, who directs the Finnish Institute for Molecular Medicine at the University of Helsinki and is a professor of genetics at Harvard Medical School. The data set has been expanded to include 125,000 people who had confirmed cases. The more informatio­n researcher­s have, the more precisely they can identify which genes are involved in making people more susceptibl­e to COVID-19 and more likely to end up hospitaliz­ed. Diversity is crucial, the researcher­s said. At least one of the genes wouldn’t have been identified if the samples had included only Europeans and Americans, Daly said.

“COVID-19 isn’t going away,” Mbarek said. “This is the biggest single genetic study in history of how people with slightly different DNA respond very differentl­y to a virus. And because for the first time a study like this has involved genetic data from all parts of the world, that data will be more powerful in spotting the right genes to help develop treatments for severe COVID or long COVID.” Health and patient safety coverage at USA TODAY is made possible in part by a grant from the Masimo Foundation for Ethics, Innovation and Competitio­n in Healthcare. The foundation does not provide editorial input.

 ?? NOAH BERGER/AP ?? Scientist Selam Bihon processes samples at the Stanford Clinical Virology Laboratory in Palo Alto, Calif.
NOAH BERGER/AP Scientist Selam Bihon processes samples at the Stanford Clinical Virology Laboratory in Palo Alto, Calif.
 ?? FRANK AUGSTEIN/AP ?? Cambridge University scientists study the genomic sequencing of the coronaviru­s.
FRANK AUGSTEIN/AP Cambridge University scientists study the genomic sequencing of the coronaviru­s.

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