| Literature DB >> 34035524 |
Laura Montefusco1, Moufida Ben Nasr2,3, Francesca D'Addio2, Cristian Loretelli2, Antonio Rossi1, Ida Pastore1, Giuseppe Daniele4, Ahmed Abdelsalam2, Anna Maestroni2, Marco Dell'Acqua2,5, Elio Ippolito2, Emma Assi2, Vera Usuelli2, Andy Joe Seelam2, Roberta Maria Fiorina2, Enrica Chebat1, Paola Morpurgo1, Maria Elena Lunati1, Andrea Mario Bolla1, Giovanna Finzi6, Reza Abdi7, Joseph V Bonventre7, Stefano Rusconi8, Agostino Riva8, Domenico Corradi9, Pierachille Santus10,11, Manuela Nebuloni12,13, Franco Folli14, Gian Vincenzo Zuccotti1,15, Massimo Galli8, Paolo Fiorina16,17,18.
Abstract
Patients with coronavirus disease 2019 (COVID-19) are reported to have a greater prevalence of hyperglycaemia. Cytokine release as a consequence of severe acute respiratory syndrome coronavirus 2 infection may precipitate the onset of metabolic alterations by affecting glucose homeostasis. Here we describe abnormalities in glycometabolic control, insulin resistance and beta cell function in patients with COVID-19 without any pre-existing history or diagnosis of diabetes, and document glycaemic abnormalities in recovered patients 2 months after onset of disease. In a cohort of 551 patients hospitalized for COVID-19 in Italy, we found that 46% of patients were hyperglycaemic, whereas 27% were normoglycaemic. Using clinical assays and continuous glucose monitoring in a subset of patients, we detected altered glycometabolic control, with insulin resistance and an abnormal cytokine profile, even in normoglycaemic patients. Glycaemic abnormalities can be detected for at least 2 months in patients who recovered from COVID-19. Our data demonstrate that COVID-19 is associated with aberrant glycometabolic control, which can persist even after recovery, suggesting that further investigation of metabolic abnormalities in the context of long COVID is warranted.Entities:
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Year: 2021 PMID: 34035524 DOI: 10.1038/s42255-021-00407-6
Source DB: PubMed Journal: Nat Metab ISSN: 2522-5812