Impaired glucose metabolism in patients with diabetes, prediabetes, and obesity is associated with severe COVID-19.


Journal

Journal of medical virology
ISSN: 1096-9071
Titre abrégé: J Med Virol
Pays: United States
ID NLM: 7705876

Informations de publication

Date de publication:
01 2021
Historique:
received: 14 06 2020
revised: 22 06 2020
accepted: 23 06 2020
pubmed: 27 6 2020
medline: 10 3 2021
entrez: 27 6 2020
Statut: ppublish

Résumé

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.

Sections du résumé

BACKGROUND
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.

Identifiants

pubmed: 32589756
doi: 10.1002/jmv.26227
pmc: PMC7361926
doi:

Substances chimiques

Blood Glucose 0
Glycated Hemoglobin A 0
Glucose IY9XDZ35W2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

409-415

Informations de copyright

© 2020 The Authors. Journal of Medical Virology published by Wiley Periodicals LLC.

Références

N Engl J Med. 2020 May 7;382(19):1787-1799
pubmed: 32187464
JAMA. 2020 Mar 17;323(11):1061-1069
pubmed: 32031570
Lancet. 2020 Mar 28;395(10229):1054-1062
pubmed: 32171076
Diabetes Metab Syndr. 2020 May - Jun;14(3):211-212
pubmed: 32172175
J Med Virol. 2021 Jan;93(1):409-415
pubmed: 32589756
J Med Virol. 2020 Jul;92(7):770-775
pubmed: 32293710
Diabet Med. 2006 Jun;23(6):623-8
pubmed: 16759303
JAMA. 2020 Jun 23;323(24):2493-2502
pubmed: 32392282
Diabetes Care. 2009 May;32(5):828-33
pubmed: 19196895
N Engl J Med. 2020 Jun 18;382(25):2411-2418
pubmed: 32379955
Lancet. 2020 May 16;395(10236):1544-1545
pubmed: 32380044
N Engl J Med. 2020 May 21;382(21):2012-2022
pubmed: 32227758
Acta Diabetol. 2010 Sep;47(3):193-9
pubmed: 19333547
Int J Mol Sci. 2017 Mar 05;18(3):
pubmed: 28273875
JAMA. 2020 Apr 28;323(16):1574-1581
pubmed: 32250385
Diabet Med. 2020 May;37(5):723-725
pubmed: 32242990
N Engl J Med. 2020 Apr 30;382(18):1708-1720
pubmed: 32109013
Cell Metab. 2020 Jun 2;31(6):1068-1077.e3
pubmed: 32369736
Diabetes Care. 2010 Jan;33 Suppl 1:S62-9
pubmed: 20042775
J Diabetes. 2020 Apr;12(4):347-348
pubmed: 32162476

Auteurs

Stephen M Smith (SM)

The Smith Center for Infectious Diseases and Urban Health, East Orange, New Jersey.

Avinash Boppana (A)

The Smith Center for Infectious Diseases and Urban Health, East Orange, New Jersey.

Julie A Traupman (JA)

The Smith Center for Infectious Diseases and Urban Health, East Orange, New Jersey.

Enrique Unson (E)

The Smith Center for Infectious Diseases and Urban Health, East Orange, New Jersey.

Daniel A Maddock (DA)

The Smith Center for Infectious Diseases and Urban Health, East Orange, New Jersey.

Kathy Chao (K)

The Smith Center for Infectious Diseases and Urban Health, East Orange, New Jersey.

David P Dobesh (DP)

Saint Barnabas Medical Center, RWJBarnabas Health, Livingston, New Jersey.

Adam Brufsky (A)

UPMC Hillman Cancer Center, Magee-Women's Hospital, University of Pittsburgh, Pittsburgh, Pennsylvania.

Ruth I Connor (RI)

Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH