Association of glycemic control with Long COVID in patients with type 2 diabetes: findings from the National COVID Cohort Collaborative (N3C).

IF 3.7 2区 医学 Q2 ENDOCRINOLOGY & METABOLISM BMJ Open Diabetes Research & Care Pub Date : 2025-02-04 DOI:10.1136/bmjdrc-2024-004536
Samuel Soff, Yun Jae Yoo, Carolyn Bramante, Jane E B Reusch, Jared Davis Huling, Margaret A Hall, Daniel Brannock, Til Sturmer, Zachary Butzin-Dozier, Rachel Wong, Richard Moffitt
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Abstract

Introduction: Elevated glycosylated hemoglobin (HbA1c) in individuals with type 2 diabetes is associated with increased risk of hospitalization and death after acute COVID-19, however the effect of HbA1c on Long COVID is unclear.

Objective: Evaluate the association of glycemic control with the development of Long COVID in patients with type 2 diabetes (T2D).

Research design and methods: We conducted a retrospective cohort study using electronic health record data from the National COVID Cohort Collaborative. Our cohort included individuals with T2D from eight sites with longitudinal natural language processing (NLP) data. The primary outcome was death or new-onset recurrent Long COVID symptoms within 30-180 days after COVID-19. Symptoms were identified as keywords from clinical notes using NLP in respiratory, brain fog, fatigue, loss of smell/taste, cough, cardiovascular and musculoskeletal symptom categories. Logistic regression was used to evaluate the risk of Long COVID by HbA1c range, adjusting for demographics, body mass index, comorbidities, and diabetes medication. A COVID-negative group was used as a control.

Results: Among 7430 COVID-positive patients, 1491 (20.1%) developed symptomatic Long COVID, and 380 (5.1%) died. The primary outcome of death or Long COVID was increased in patients with HbA1c 8% to <10% (OR 1.20, 95% CI 1.02 to 1.41) and ≥10% (OR 1.40, 95% CI 1.14 to 1.72) compared with those with HbA1c 6.5% to <8%. This association was not seen in the COVID-negative group. Higher HbA1c levels were associated with increased risk of Long COVID symptoms, especially respiratory and brain fog. There was no association between HbA1c levels and risk of death within 30-180 days following COVID-19. NLP identified more patients with Long COVID symptoms compared with diagnosis codes.

Conclusion: Poor glycemic control (HbA1c≥8%) in people with T2D was associated with higher risk of Long COVID symptoms 30-180 days following COVID-19. Notably, this risk increased as HbA1c levels rose. However, this association was not observed in patients with T2D without a history of COVID-19. An NLP-based definition of Long COVID identified more patients than diagnosis codes and should be considered in future studies.

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2 型糖尿病患者血糖控制与 Long COVID 的关系:全国 COVID 队列协作组织 (N3C) 的研究结果。
导言:2 型糖尿病患者的糖化血红蛋白(HbA1c)升高与急性 COVID-19 后住院和死亡风险增加有关,但 HbA1c 对长 COVID 的影响尚不清楚:评估血糖控制与 2 型糖尿病(T2D)患者发生长 COVID 的关系:我们利用国家 COVID 队列协作组织的电子健康记录数据开展了一项回顾性队列研究。我们的队列包括来自 8 个地点的 T2D 患者,他们都拥有纵向自然语言处理 (NLP) 数据。主要结果是在 COVID-19 后 30-180 天内死亡或新发复发的 Long COVID 症状。使用 NLP 将临床笔记中的症状识别为呼吸、脑雾、疲劳、嗅觉/味觉丧失、咳嗽、心血管和肌肉骨骼症状类别中的关键词。在调整人口统计学、体重指数、合并症和糖尿病药物的基础上,采用 Logistic 回归评估 HbA1c 范围的长 COVID 风险。COVID阴性组作为对照组:在 7430 名 COVID 阳性患者中,有 1491 人(20.1%)出现症状性长 COVID,380 人(5.1%)死亡。在 HbA1c 为 8%至结论的患者中,死亡或 Long COVID 的主要结果有所增加:血糖控制不佳(HbA1c≥8%)的 T2D 患者在 COVID-19 后 30-180 天内出现 Long COVID 症状的风险较高。值得注意的是,这种风险随着 HbA1c 水平的升高而增加。然而,在没有 COVID-19 病史的 T2D 患者中却没有观察到这种关联。基于 NLP 的长 COVID 定义比诊断代码识别出的患者更多,在未来的研究中应加以考虑。
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来源期刊
BMJ Open Diabetes Research & Care
BMJ Open Diabetes Research & Care Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
9.30
自引率
2.40%
发文量
123
审稿时长
18 weeks
期刊介绍: BMJ Open Diabetes Research & Care is an open access journal committed to publishing high-quality, basic and clinical research articles regarding type 1 and type 2 diabetes, and associated complications. Only original content will be accepted, and submissions are subject to rigorous peer review to ensure the publication of high-quality — and evidence-based — original research articles.
期刊最新文献
Association of glycemic control with Long COVID in patients with type 2 diabetes: findings from the National COVID Cohort Collaborative (N3C). Retraction: Circulating long non-coding RNAs NKILA, NEAT1, MALAT1, and MIAT expression and their association in type 2 diabetes mellitus. Ethnic disparities in HbA1c and hypoglycemia among youth with type 1 diabetes: beyond access to technology, social deprivation and mean blood glucose. Association between use of sodium-glucose co-transporter-2 inhibitor and the risk of incident dementia: a population-based cohort study. Mechanism of TGIF1 on glycolipid metabolism disorders in mice with type 2 diabetes.
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