The world’s largest study of the genetics of critical COVID-19, involving more than 57,000 people, has revealed fresh details about some of the biological mechanisms behind the severe form of the disease. Some 16 new genetic variants associated with severe COVID-19 have been identified, including some related to blood clotting, immune response and intensity of inflammation.
Experts say the findings will act as a roadmap for future efforts, opening new fields of research focused on potential new therapies and diagnostics with pinpoint accuracy.
The study was conducted by the GenOMICC consortium – a global collaboration to study genetics in critical illness, led by University of Edinburgh in partnership with Genomics England. It was led in Ireland by Professor Alistair Nichol, Chair of Critical Care Medicine, UCD School of Medicine, Consultant at St Vincent’s University Hospital, and Director of the Irish Critical Care-Clinical Trials Network, based at UCD. It was funded in Ireland by the Health Research Board and endorsed by the Irish Critical Care-Clinical Trials Group.
Researchers made the recent discoveries by sequencing the genomes of 7,491 patients from 224 intensive care units in the UK and Ireland. Their DNA was compared with 48,400 other people who had not had COVID-19, participants in Genomics England's 100,000 Genomes Project and that of a further 1,630 people who had experienced mild covid.
Determining the whole genome sequence for all participants in the study allowed the team to create a precise map and identify genetic variation linked to severity of COVID-19. The team found key differences in 16 genes in the ICU patients when compared with the DNA of the other groups. They also confirmed the involvement of seven other genetic variations already associated with severe COVID-19 discovered in earlier studies from the same team.
The findings included how a single gene variant that disrupts a key messenger molecule in immune system signaling – called interferon alpha-10 – was enough to increase a patient’s risk of severe disease. This highlights the gene’s key role in the immune system and suggests that treating patients with interferon – proteins released by immune cells to defend against viruses – may help manage disease in the early stages.
The study also found that variations in genes that control the levels of a central component of blood clotting – known as Factor 8 – were associated with critical illness in Covid-19. This may explain some of the clotting abnormalities that are seen in severe cases of COVID-19. Factor 8 is the gene underlying the most common type of haemophilia.
Chief investigator and a Consultant in Critical Care Medicine at University of Edinburgh, Professor Kenneth Baillie said: “Our latest findings point to specific molecular targets in critical COVID-19. These results explain why some people develop life-threatening COVID-19, while others get no symptoms at all. But more importantly, this gives us a deep understanding of the process of disease and is a big step forward in finding more effective treatments. It is now true to say that we understand the mechanisms of covid better than the other syndromes we treat in intensive care in normal times – sepsis, flu, and other forms of critical illness. COVID-19 is showing us the way to tackle those problems in the future.”
Co-author on the study, Professor Alistair Nichol said: “This study allows us to identify targets for novel or repurposed therapeutics to improve outcomes in the critically ill covid patient. Trials like REMAP-CAP have already demonstrated that agents aimed at these targets, inflammation and anticoagulation, can improve outcomes. This study gives us trialists a much greater range of targets for the future. Covid will be with us for a long time and we need to continue to increase our range of therapeutics.”
Co-author and former Chief Scientist at Genomics England, from Queen Mary University of London, Professor Sir Mark Caulfield said: “As COVID-19 evolves, we need to focus on reducing the number of people getting seriously ill and being hospitalised. Through our whole genome sequencing research, we’ve discovered novel gene variants that predispose people to severe illness – which now offer a route to new tests and treatments, to help protect the public and the NHS from this virus.”
Chief Medical Officer at Genomics England, Dr Rich Scott said: “Strategically, we’re at a point where genomic science is becoming an integral part of the national infrastructure in routine healthcare. This study illustrates the value of whole genome sequencing to detect rare and common variants that influence critical illness requiring intensive care. It represents a major leap forward in our understanding of how our genetic makeup influences severe illness with COVID-19. All those involved in the study went to great efforts to engage with all communities within the UK – including groups that have historically been under-represented in medical studies. The inclusive element of our work has generated meaningful results for everyone in the country.”
The findings have been published in Nature: https://www.nature.com/articles/s41586-022-04576-6
GenOMICC (Genetics of Susceptibility and Mortality in Critical Care) started in 2015 as an open, global consortium of intensive care clinicians dedicated to understanding genetic factors influencing outcomes in intensive care from diseases such as SARS, flu and sepsis.
The consortium is led by the University of Edinburgh, and since 2020 it has been focused on Covid-19 research in partnership with Genomics England and in collaboration with NHS Lothian, the Intensive Care National Audit and Research Centre (ICNARC), and Queen Mary University of London. The study is led in Ireland by Prof Alistair Nichol, Director of the Irish Critical Care Clinical Trials Network at University College Dublin and funded in Ireland by the Health Research Board and was endorsed by the Irish Critical Care-Clinical Trials Group.