Journal of Medical Virology, volume 93, issue 1, pages 409-415
Impaired glucose metabolism in patients with diabetes, prediabetes, and obesity is associated with severe COVID‐19
Stephen M Smith
1
,
Avinash Boppana
1
,
Julie A Traupman
1
,
Enrique Unson
1
,
Daniel A Maddock
1
,
Kathy Chao
1
,
David P Dobesh
2
,
Adam Brufsky
3
,
Ruth I. Connor
4
1
The Smith Center for Infectious Diseases and Urban Health East Orange New Jersey
|
2
Saint Barnabas Medical Center RWJBarnabas Health Livingston New Jersey
|
3
Publication type: Journal Article
Publication date: 2020-07-17
Journal:
Journal of Medical Virology
scimago Q1
SJR: 1.560
CiteScore: 23.2
Impact factor: 6.8
ISSN: 01466615, 10969071
PubMed ID:
32589756
Infectious Diseases
Virology
Abstract
Identification of risk factors of severe coronavirus disease 2019 (COVID-19) is critical for improving therapies and understanding severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pathogenesis. We analyzed 184 patients hospitalized for COVID-19 in Livingston, New Jersey for clinical characteristics associated with severe disease. The majority of patients with COVID-19 had diabetes mellitus (DM) (62.0%), Pre-DM (23.9%) with elevated fasting blood glucose (FBG), or a body mass index >30 with normal hemoglobin A1c (HbA1C) (4.3%). SARS-CoV-2 infection was associated with new and persistent hyperglycemia in 29 patients, including several with normal HbA1C levels. Forty-four patients required intubation, which occurred significantly more often in patients with DM as compared with non-diabetics. Severe COVID-19 occurs in the presence of impaired glucose metabolism in patients, including those with DM, preDM, and obesity. COVID-19 is associated with elevated FBG and several patients presented with new onset DM or in DKA. The association of dysregulated glucose metabolism and severe COVID-19 suggests that SARS-CoV-2 pathogenesis involves a novel interplay with glucose metabolism. Exploration of pathways by which SARS-CoV-2 interacts glucose metabolism is critical for understanding disease pathogenesis and developing therapies.
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