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Published on: July 14, 2016
Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality
Tomoko Nakanishi1,2,3,4,5, Sara Pigazzini1,6, Frauke Degenhardt7,8
1Institute for Molecular Medicine Finland, Univerisity of Helsinki, Helsinki, Finland.
Insights
A common genetic marker on chromosome 3 increases COVID-19 severity and mortality risk, particularly in individuals under 60. This genetic factor
Area of Science:
- Genetics
- Infectious Diseases
- Epidemiology
Background:
- COVID-19 outcomes show significant variability, potentially influenced by genetic factors.
- A major genetic risk factor for COVID-19 severity is located on chromosome 3.
- The age-dependent effects of this genetic predisposition require detailed characterization.
Conclusions:
- The chromosome 3 COVID-19 risk locus significantly increases morbidity and mortality.
- These risks are amplified in individuals ≤ 60 years, highlighting an age-dependent genetic effect.
- The genetic factor's impact rivals established clinical risk factors, suggesting implications for risk management.
Background:
There is considerable variability in COVID-19 outcomes amongst younger adults-and some of this variation may be due to genetic predisposition. We characterized the clinical implications of the major genetic risk factor for COVID-19 severity, and its age-dependent effect, using individual-level data in a large international multi-centre consortium.
Method:
The major common COVID-19 genetic risk factor is a chromosome 3 locus, tagged by the marker rs10490770. We combined individual level data for 13,424 COVID-19 positive patients (N=6,689 hospitalized) from 17 cohorts in nine countries to assess the association of this genetic marker with mortality, COVID-19-related complications and laboratory values. We next examined if the magnitude of these associations varied by age and were independent from known clinical COVID-19 risk factors.
Findings:
We found that rs10490770 risk allele carriers experienced an increased risk of all-cause mortality (hazard ratio [HR] 1·4, 95% confidence interval [CI] 1·2-1·6) and COVID-19 related mortality (HR 1·5, 95%CI 1·3-1·8). Risk allele carriers had increased odds of several COVID-19 complications: severe respiratory failure (odds ratio [OR] 2·0, 95%CI 1·6-2·6), venous thromboembolism (OR 1·7, 95%CI 1·2-2·4), and hepatic injury (OR 1·6, 95%CI 1·2-2·0). Risk allele carriers ≤ 60 years had higher odds of death or severe respiratory failure (OR 2·6, 95%CI 1·8-3·9) compared to those > 60 years OR 1·5 (95%CI 1·3-1·9, interaction p-value=0·04). Amongst individuals ≤ 60 years who died or experienced severe respiratory COVID-19 outcome, we found that 31·8% (95%CI 27·6-36·2) were risk variant carriers, compared to 13·9% (95%CI 12·6-15·2%) of those not experiencing these outcomes. Prediction of death or severe respiratory failure among those ≤ 60 years improved when including the risk allele (AUC 0·82 vs 0·84, p=0·016) and the prediction ability of rs10490770 risk allele was similar to, or better than, most established clinical risk factors.
Interpretation:
The major common COVID-19 risk locus on chromosome 3 is associated with increased risks of morbidity and mortality-and these are more pronounced amongst individuals ≤ 60 years. The effect on COVID-19 severity was similar to, or larger than most established risk factors, suggesting potential implications for clinical risk management.
Funding:
Funding was obtained by each of the participating cohorts individually.
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