Cardiometabolic risks of SARS-CoV-2 hospitalization using Mendelian Randomization

Sci Rep. 2021 Apr 12;11(1):7848. doi: 10.1038/s41598-021-86757-3.

Abstract

Many cardiometabolic conditions have demonstrated associative evidence with COVID-19 hospitalization risk. However, the observational designs of the studies in which these associations are observed preclude causal inferences of hospitalization risk. Mendelian Randomization (MR) is an alternative risk estimation method more robust to these limitations that allows for causal inferences. We applied four MR methods (MRMix, IMRP, IVW, MREgger) to publicly available GWAS summary statistics from European (COVID-19 GWAS n = 2956) and multi-ethnic populations (COVID-19 GWAS n = 10,908) to better understand extant causal associations between Type II Diabetes (GWAS n = 659,316), BMI (n = 681,275), diastolic and systolic blood pressure, and pulse pressure (n = 757,601 for each) and COVID-19 hospitalization risk across populations. Although no significant causal effect evidence was observed, our data suggested a trend of increasing hospitalization risk for Type II diabetes (IMRP OR, 95% CI 1.67, 0.96-2.92) and pulse pressure (OR, 95% CI 1.27, 0.97-1.66) in the multi-ethnic sample. Type II diabetes and Pulse pressure demonstrates a potential causal association with COVID-19 hospitalization risk, the proper treatment of which may work to reduce the risk of a severe COVID-19 illness requiring hospitalization. However, GWAS of COVID-19 with large sample size is warranted to confirm the causality.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Alleles
  • Blood Pressure
  • Body Mass Index
  • COVID-19 / genetics*
  • COVID-19 / therapy*
  • Cardiology
  • Cardiovascular Diseases / therapy*
  • Diabetes Mellitus, Type 2 / complications
  • Ethnicity
  • Genome-Wide Association Study
  • Hospitalization
  • Humans
  • Likelihood Functions
  • Mendelian Randomization Analysis*
  • Polymorphism, Single Nucleotide
  • Pulse
  • Risk Factors