Lee Bohee, Man Kenneth K C, Wong Ernie, Tan Tricia, Sheikh Aziz, Bloom Chloe I
National Heart and Lung Institute, Imperial College London, London, England.
Research Department of Practice and Policy, School of Pharmacy, University College London, London, England.
JAMA Intern Med. 2025 Jan 1;185(1):16-25. doi: 10.1001/jamainternmed.2024.5982.
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.
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.
The primary exposure was metformin; secondary exposures included add-on antidiabetic medications.
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.
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).
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.
在哮喘患者中,体重指数(BMI)升高和2型糖尿病很常见,且与哮喘发作风险增加相关。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)减轻了气道炎症、高反应性和重塑。然而,流行病学证据有限。
评估二甲双胍及附加抗糖尿病药物(GLP-1RA、二肽基肽酶-4抑制剂、磺脲类药物、钠-葡萄糖协同转运蛋白-2抑制剂和胰岛素)与哮喘发作的关联。
设计、背景和参与者:该研究使用了英国临床实践研究数据链(CPRD)Aurum中2004年至2020年的医院入院和死亡率数据。采用了一种三角测量法,应用两种不同方法以增强稳健性:自控病例系列(SCCS)和使用治疗加权逆概率(IPTW)的二甲双胍新用户队列。符合条件的参与者为2型糖尿病二甲双胍新用户。为评估代谢表型(BMI、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。进行了阴性对照分析以评估偏倚。
主要暴露为二甲双胍;次要暴露包括附加抗糖尿病药物。
主要结局为12个月随访期间的首次哮喘加重(短期口服糖皮质激素、非计划的与哮喘相关的医院就诊或死亡)。在SCCS中使用固定效应条件泊松模型估计发病率比(IRR)及95%置信区间,在队列中使用加权Cox比例风险模型估计风险比(HR)。
在超过200万成年哮喘患者中,4278例患者(2617名女性[61.2%];平均[标准差]年龄,52.9[13.6]岁)被纳入SCCS,8424例患者(4690名女性[55.7%];未暴露组:平均[标准差]年龄,61.6[13.2]岁;暴露组:平均[标准差]年龄,59.7[13.7]岁)被纳入IPTW队列。在两种方法中均发现二甲双胍与较少的类似程度哮喘发作相关(SCCS:IRR,0.68;95%置信区间,0.62 - 0.75;IPTW:HR,0.76;95%置信区间,0.67 - 0.85)。阴性对照分析未发现显著偏倚的证据。糖化血红蛋白水平、BMI、血液嗜酸性粒细胞计数和哮喘严重程度并未改变这种关联。唯一具有相加关联的附加抗糖尿病药物是GLP-1RA(SCCS:IRR,0.60;95%置信区间,0.49 - 0.73)。
这项队列研究结果表明,二甲双胍与较低的哮喘发作率相关,联合使用GLP-1RA可进一步降低发作率。这似乎与血糖控制或体重减轻以外的机制相关,且在各种哮喘表型中均有发生。