Diabetes, obesity, metabolism, and SARS-CoV-2 infection: the end of the beginning

Cell Metab. 2021 Mar 2;33(3):479-498. doi: 10.1016/j.cmet.2021.01.016. Epub 2021 Jan 21.

Abstract

The increased prevalence of obesity, diabetes, and cardiovascular risk factors in people hospitalized with severe COVID-19 illness has engendered considerable interest in the metabolic aspects of SARS-CoV-2-induced pathophysiology. Here, I update concepts informing how metabolic disorders and their co-morbidities modify the susceptibility to, natural history, and potential treatment of SARS-CoV-2 infection, with a focus on human biology. New data informing genetic predisposition, epidemiology, immune responses, disease severity, and therapy of COVID-19 in people with obesity and diabetes are highlighted. The emerging relationships of metabolic disorders to viral-induced immune responses and viral persistence, and the putative importance of adipose and islet ACE2 expression, glycemic control, cholesterol metabolism, and glucose- and lipid-lowering drugs is reviewed, with attention to controversies and unresolved questions. Rapid progress in these areas informs our growing understanding of SARS-CoV-2 infection in people with diabetes and obesity, while refining the therapeutic strategies and research priorities in this vulnerable population.

Keywords: adipose tissue; glucose; immunity; islet; vaccination; virus.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Angiotensin-Converting Enzyme 2 / metabolism
  • Blood Glucose / analysis
  • COVID-19 / epidemiology
  • COVID-19 / pathology*
  • COVID-19 Drug Treatment
  • Cholesterol / metabolism
  • Comorbidity
  • Diabetes Mellitus / pathology*
  • Genetic Predisposition to Disease / genetics
  • Glucose / metabolism
  • Heart Disease Risk Factors*
  • Humans
  • Hyperglycemia / pathology
  • Metabolic Diseases / pathology*
  • Obesity / pathology*
  • SARS-CoV-2

Substances

  • Blood Glucose
  • Cholesterol
  • ACE2 protein, human
  • Angiotensin-Converting Enzyme 2
  • Glucose