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Association of COVID-19 with diabetes: a systematic review and meta-analysis

Emerging evidence suggests that coronavirus disease-2019 (COVID-19) may lead to a wide range of post-acute sequelae outcomes, including new onset of diabetes. The aim of this meta-analysis was to estimate the incidence of newly diagnosed diabetes in survivors of COVID-19. We searched MEDLINE, Scopus...

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Autores principales: Ssentongo, Paddy, Zhang, Yue, Witmer, Lisa, Chinchilli, Vernon M., Ba, Djibril M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9684130/
https://www.ncbi.nlm.nih.gov/pubmed/36418912
http://dx.doi.org/10.1038/s41598-022-24185-7
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author Ssentongo, Paddy
Zhang, Yue
Witmer, Lisa
Chinchilli, Vernon M.
Ba, Djibril M.
author_facet Ssentongo, Paddy
Zhang, Yue
Witmer, Lisa
Chinchilli, Vernon M.
Ba, Djibril M.
author_sort Ssentongo, Paddy
collection PubMed
description Emerging evidence suggests that coronavirus disease-2019 (COVID-19) may lead to a wide range of post-acute sequelae outcomes, including new onset of diabetes. The aim of this meta-analysis was to estimate the incidence of newly diagnosed diabetes in survivors of COVID-19. We searched MEDLINE, Scopus, Cochrane Central Register of Controlled Trials and the World Health Organization Global Literature on Coronavirus Disease and clinical trial registries for studies reporting the association of COVID-19 and diabetes. Search dates were December 2019–October 16, 2022. Two investigators independently assessed studies for inclusion. Risk of bias was assessed using the Newcastle–Ottawa Scale. We estimated the effect of COVID-19 on incident diabetes by random-effects meta-analyses using the generic inverse variance method. We identified 8 eligible studies consisting of 4,270,747 COVID-19 patients and 43,203,759 controls. Median age was 43 years (interquartile range, IQR 35–49), and 50% were female. COVID-19 was associated with a 66% higher risk of incident diabetes (risk ratio, 1.66; 95% CI 1.38; 2.00). The risk was not modified by age, sex, or study quality. The median risk of bias assessment was 7. In this systematic review and meta-analysis, COVID-19 was associated with higher risk for developing new onset diabetes among survivors. Active monitoring of glucose dysregulation after recovery from severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is warranted.
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spelling pubmed-96841302022-11-25 Association of COVID-19 with diabetes: a systematic review and meta-analysis Ssentongo, Paddy Zhang, Yue Witmer, Lisa Chinchilli, Vernon M. Ba, Djibril M. Sci Rep Article Emerging evidence suggests that coronavirus disease-2019 (COVID-19) may lead to a wide range of post-acute sequelae outcomes, including new onset of diabetes. The aim of this meta-analysis was to estimate the incidence of newly diagnosed diabetes in survivors of COVID-19. We searched MEDLINE, Scopus, Cochrane Central Register of Controlled Trials and the World Health Organization Global Literature on Coronavirus Disease and clinical trial registries for studies reporting the association of COVID-19 and diabetes. Search dates were December 2019–October 16, 2022. Two investigators independently assessed studies for inclusion. Risk of bias was assessed using the Newcastle–Ottawa Scale. We estimated the effect of COVID-19 on incident diabetes by random-effects meta-analyses using the generic inverse variance method. We identified 8 eligible studies consisting of 4,270,747 COVID-19 patients and 43,203,759 controls. Median age was 43 years (interquartile range, IQR 35–49), and 50% were female. COVID-19 was associated with a 66% higher risk of incident diabetes (risk ratio, 1.66; 95% CI 1.38; 2.00). The risk was not modified by age, sex, or study quality. The median risk of bias assessment was 7. In this systematic review and meta-analysis, COVID-19 was associated with higher risk for developing new onset diabetes among survivors. Active monitoring of glucose dysregulation after recovery from severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is warranted. Nature Publishing Group UK 2022-11-23 /pmc/articles/PMC9684130/ /pubmed/36418912 http://dx.doi.org/10.1038/s41598-022-24185-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Ssentongo, Paddy
Zhang, Yue
Witmer, Lisa
Chinchilli, Vernon M.
Ba, Djibril M.
Association of COVID-19 with diabetes: a systematic review and meta-analysis
title Association of COVID-19 with diabetes: a systematic review and meta-analysis
title_full Association of COVID-19 with diabetes: a systematic review and meta-analysis
title_fullStr Association of COVID-19 with diabetes: a systematic review and meta-analysis
title_full_unstemmed Association of COVID-19 with diabetes: a systematic review and meta-analysis
title_short Association of COVID-19 with diabetes: a systematic review and meta-analysis
title_sort association of covid-19 with diabetes: a systematic review and meta-analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9684130/
https://www.ncbi.nlm.nih.gov/pubmed/36418912
http://dx.doi.org/10.1038/s41598-022-24185-7
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