Antidiabetic Medication and Asthma Attacks.

IF 22.5 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Bohee Lee, Kenneth K C Man, Ernie Wong, Tricia Tan, Aziz Sheikh, Chloe I Bloom
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引用次数: 0

Abstract

Importance: Elevated body mass index (BMI) and type 2 diabetes are prevalent in asthma and are associated with an increase in the risk of asthma attacks. In experimental studies, the diabetes medications metformin and glucagon-like peptide-1 receptor agonists (GLP-1RA) have mitigated airway inflammation, hyperresponsiveness, and remodeling. However, epidemiological evidence is limited.

Objective: To estimate the association of metformin and add-on antidiabetic medications (GLP-1RA, dipeptidyl peptidase-4 inhibitors, sulphonylureas, sodium-glucose cotransporter-2 inhibitors, and insulin) with asthma attacks.

Design, setting, and participants: The study used data from the UK Clinical Practice Research Datalink (CPRD) Aurum linked hospital admissions and mortality data from 2004 to 2020. A triangulation approach was used that applied 2 distinct approaches to enhance robustness: a self-controlled case series (SCCS) and a metformin new user cohort with inverse probability of treatment weighting (IPTW). Eligible participants were new users of metformin with type 2 diabetes. To evaluate the association between metabolic phenotypes (BMI, glycemic control) and asthma phenotypes (type 2 inflammation, asthma severity), interaction analyses were conducted. Negative control analyses were conducted to assess for bias.

Exposure: The primary exposure was metformin; secondary exposures included add-on antidiabetic medications.

Main outcomes: The primary outcome was first asthma exacerbation (short course of oral corticosteroids, unscheduled asthma-related hospital attendance, or death) during 12-month follow-up. Incidence rate ratios (IRRs) with 95% CIs were estimated using fixed-effect conditional Poisson models in the SCCS, and hazard ratios (HRs) were estimated using weighted Cox proportional hazards models in the cohort.

Results: Of more than 2 million adults with asthma, 4278 patients (2617 women [61.2%]; mean [SD] age, 52.9 [13.6] years) were identified for the SCCS and 8424 patients (4690 women [55.7%]; unexposed: mean [SD] age, 61.6 [13.2] years; exposed: mean [SD] age, 59.7 [13.7] years) for the IPTW cohort. Metformin was found to be associated with fewer asthma attacks of similar magnitude in both approaches (SCCS: IRR, 0.68; 95% CI, 0.62-0.75; IPTW: HR, 0.76; 95% CI, 0.67-0.85). Negative control analyses did not find evidence of significant bias. Hemoglobin A1c levels, BMI, blood eosinophil cell counts, and asthma severity did not modify the association. The only add-on antidiabetic medication to have an additive association was GLP-1RA (SCCS: IRR, 0.60; 95% CI, 0.49-0.73).

Conclusions and relevance: The results of this cohort study suggest that metformin was associated with a lower rate of asthma attacks, with further reductions with the use of GLP-1RA. This appeared to be associated with mechanisms other than through glycemic control or weight loss and occurred across asthma phenotypes.

抗糖尿病药物与哮喘发作
重要性:体重指数(BMI)升高和 2 型糖尿病是哮喘的常见病,与哮喘发作风险的增加有关。在实验研究中,糖尿病药物二甲双胍和胰高血糖素样肽-1 受体激动剂(GLP-1RA)可减轻气道炎症、高反应性和重塑。然而,流行病学证据却很有限:目的:评估二甲双胍和附加抗糖尿病药物(GLP-1RA、二肽基肽酶-4 抑制剂、磺脲类药物、钠-葡萄糖共转运体-2 抑制剂和胰岛素)与哮喘发作的关系:研究使用的数据来自英国临床实践研究数据链(CPRD)Aurum 2004 年至 2020 年的入院和死亡链接数据。研究采用三角测量法,应用两种不同的方法来增强稳健性:自控病例系列(SCCS)和二甲双胍新用户队列,并采用反向治疗概率加权法(IPTW)。符合条件的参与者均为二甲双胍新用户,且患有 2 型糖尿病。为评估代谢表型(体重指数、血糖控制)与哮喘表型(2型炎症、哮喘严重程度)之间的关联,进行了交互分析。暴露:主要暴露是二甲双胍;次要暴露包括附加的抗糖尿病药物:主要结果:在12个月的随访期间,首次哮喘加重(短期口服皮质类固醇、与哮喘相关的计划外住院或死亡)为主要结果。在 SCCS 中使用固定效应条件泊松模型估算发病率比(IRRs)及 95% CIs,在队列中使用加权 Cox 比例危险模型估算危险比(HRs):在 200 多万名成人哮喘患者中,SCCS 确定了 4278 名患者(2617 名女性 [61.2%];平均 [SD] 年龄 52.9 [13.6] 岁),IPTW 队列确定了 8424 名患者(4690 名女性 [55.7%];未暴露:平均 [SD] 年龄 61.6 [13.2] 岁;暴露:平均 [SD] 年龄 59.7 [13.7] 岁)。在两种方法中,二甲双胍与哮喘发作次数减少的相关性相似(SCCS:IRR,0.68;95% CI,0.62-0.75;IPTW:HR,0.76;95% CI,0.67-0.85)。阴性对照分析未发现明显偏倚的证据。血红蛋白 A1c 水平、体重指数(BMI)、血液嗜酸性粒细胞计数和哮喘严重程度并未改变相关性。唯一具有附加关联性的附加抗糖尿病药物是 GLP-1RA(SCCS:IRR,0.60;95% CI,0.49-0.73):这项队列研究的结果表明,二甲双胍与较低的哮喘发作率有关,使用 GLP-1RA 会进一步降低哮喘发作率。这似乎与血糖控制或体重减轻以外的机制有关,并且发生在不同的哮喘表型中。
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来源期刊
JAMA Internal Medicine
JAMA Internal Medicine MEDICINE, GENERAL & INTERNAL-
CiteScore
43.50
自引率
1.30%
发文量
371
期刊介绍: JAMA Internal Medicine is an international, peer-reviewed journal committed to advancing the field of internal medicine worldwide. With a focus on four core priorities—clinical relevance, clinical practice change, credibility, and effective communication—the journal aims to provide indispensable and trustworthy peer-reviewed evidence. Catering to academics, clinicians, educators, researchers, and trainees across the entire spectrum of internal medicine, including general internal medicine and subspecialties, JAMA Internal Medicine publishes innovative and clinically relevant research. The journal strives to deliver stimulating articles that educate and inform readers with the latest research findings, driving positive change in healthcare systems and patient care delivery. As a member of the JAMA Network, a consortium of peer-reviewed medical publications, JAMA Internal Medicine plays a pivotal role in shaping the discourse and advancing patient care in internal medicine.
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