Risks and burdens of incident diabetes in long COVID: a cohort study

被引:332
作者
Xie, Yan [1 ,3 ,4 ]
Al-Aly, Ziyad [1 ,2 ,4 ,5 ,6 ,7 ]
机构
[1] VA St Louis Hlth Care Syst, Clin Epidemiol Ctr, Res & Dev Serv, St Louis, MO USA
[2] VA St Louis Hlth Care Syst, Nephrol Sect, Med Serv, St Louis, MO USA
[3] St Louis Univ, Dept Epidemiol & Biostat, Coll Publ Hlth & Social Justice, St Louis, MO 63103 USA
[4] Vet Res & Educ Fdn St Louis, St Louis, MO USA
[5] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
[6] Washington Univ, Inst Publ Hlth, St Louis, MO 63110 USA
[7] VA St Louis Hlth Care Syst, Dev Serv, Clin Epidemiol Ctr, St Louis, MO 63011 USA
关键词
SARS-COV-2; INFECTION; CELLS;
D O I
10.1016/S2213-8587(22)00044-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background There is growing evidence suggesting that beyond the acute phase of SARS-CoV-2 infection, people with COVID-19 could experience a wide range of post-acute sequelae, including diabetes. However, the risks and burdens of diabetes in the post-acute phase of the disease have not yet been comprehensively characterised. To address this knowledge gap, we aimed to examine the post-acute risk and burden of incident diabetes in people who survived the first 30 days of SARS-CoV-2 infection. Methods In this cohort study, we used the national databases of the US Department of Veterans Affairs to build a cohort of 181 280 participants who had a positive COVID-19 test between March 1, 2020, and Sept 30, 2021, and survived the first 30 days of COVID-19; a contemporary control (n=4 118 441) that enrolled participants between March 1, 2020, and Sept 30, 2021; and a historical control (n=4 286 911) that enrolled participants between March 1, 2018, and Sept 30, 2019. Both control groups had no evidence of SARS-CoV-2 infection. Participants in all three comparison groups were free of diabetes before cohort entry and were followed up for a median of 352 days (IQR 245-406). We used inverse probability weighted survival analyses, including predefined and algorithmically selected high dimensional variables, to estimate post-acute COVID-19 risks of incident diabetes, antihyperglycaemic use, and a composite of the two outcomes. We reported two measures of risk: hazard ratio (HR) and burden per 1000 people at 12 months. Findings In the post-acute phase of the disease, compared with the contemporary control group, people with COVID-19 exhibited an increased risk (HR 1.40, 95% CI 1.36-1.44) and excess burden (13.46, 95% CI 12.11-14.84, per 1000 people at 12 months) of incident diabetes; and an increased risk (1.85, 1.78-1.92) and excess burden (12.35, 11.36-13.38) of incident antihyperglycaemic use. Additionally, analyses to estimate the risk of a composite endpoint of incident diabetes or antihyperglycaemic use yielded a HR of 1.46 (95% CI 1.43-1.50) and an excess burden of 18.03 (95% CI 16.59-19.51) per 1000 people at 12 months. Risks and burdens of post-acute outcomes increased in a graded fashion according to the severity of the acute phase of COVID-19 (whether patients were non-hospitalised, hospitalised, or admitted to intensive care). All the results were consistent in analyses using the historical control as the reference category. Interpretation In the post-acute phase, we report increased risks and 12-month burdens of incident diabetes and antihyperglycaemic use in people with COVID-19 compared with a contemporary control group of people who were enrolled during the same period and had not contracted SARS-CoV-2, and a historical control group from a pre-pandemic era. Post-acute COVID-19 care should involve identification and management of diabetes. Copyright (C) 2022 Elsevier Ltd. All rights reserved.
引用
收藏
页码:311 / 321
页数:11
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