Impacts of COVID-19 on Glycemia and Risk of Diabetic Ketoacidosis

被引:5
|
作者
Sharma, Anukriti [1 ]
Misra-Hebert, Anita D. D. [1 ,2 ,3 ]
Mariam, Arshiya [1 ]
Milinovich, Alex [1 ]
Onuzuruike, Anthony [4 ]
Koomson, Wilhemina [4 ]
Kattan, Michael W. W. [1 ]
Pantalone, Kevin M. M. [5 ]
Rotroff, Daniel M. M. [1 ,4 ,5 ]
机构
[1] Cleveland Clin, Lerner Res Inst, Dept Quantitat Hlth Sci, Cleveland Hts, OH 44118 USA
[2] Cleveland Clin, Dept Internal Med, Cleveland Clin Community Care, Cleveland Hts, OH USA
[3] Cleveland Clin, Healthcare Delivery & Implementat Sci Ctr, Cleveland Hts, OH USA
[4] Case Western Reserve Univ, Cleveland Clin Lerner Coll Med, Cleveland Hts, OH 44106 USA
[5] Cleveland Clin, Endocrinol & Metab Inst, Cleveland Hts, OH 44118 USA
关键词
CELLS;
D O I
10.2337/db22-0264
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Reports indicate that coronavirus disease 2019 (COVID-19) may impact pancreatic function and increase type 2 diabetes (T2D) risk, although real-world COVID-19 impacts on HbA(1c) and T2D are unknown. We tested whether COVID-19 increased HbA(1c), risk of T2D, or diabetic ketoacidosis (DKA). We compared pre- and post-COVID-19 HbA(1c) and T2D risk in a large real-world clinical cohort of 8,755 COVID-19(+) patients and 11,998 COVID-19(-) matched control subjects. We investigated whether DKA risk was modified in COVID-19(+) patients with type 1 diabetes (T1D) (N = 701) or T2D (N = 21,830), or by race and sex. We observed a statistically significant, albeit clinically insignificant, HbA(1c) increase post-COVID-19 (all patients Delta HbA(1c) = 0.06%; with T2D Delta HbA(1c) = 0.1%) and no increase among COVID-19(-) patients. COVID-19(+) patients were 40% more likely to be diagnosed with T2D compared with COVID-19(-) patients and 28% more likely for the same HbA(1c) change as COVID-19(-) patients, indicating that COVID-19-attributed T2D risk may be due to increased recognition during COVID-19 management. DKA in COVID-19(+) patients with T1D was not increased. COVID-19(+) Black patients with T2D displayed disproportionately increased DKA risk (hazard ratio 2.46 [95% CI 1.48-6.09], P = 0.004) compared with White patients, suggesting a need for further clinical awareness and investigation.
引用
收藏
页码:627 / 637
页数:11
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