钠-葡萄糖协同转运蛋白2抑制剂对2型糖尿病患者慢性阻塞性肺疾病急性加重的影响:一项荟萃分析和贝叶斯敏感性分析。

Effect of SGLT-2 inhibitors on COPD exacerbations in individuals with type 2 diabetes: A meta-analysis and Bayesian sensitivity analysis.

作者信息

Shabil Muhammed, Patil Jayaraj, Satapathy Prakasini, Gaidhane Abhay M, Chennakesavulu Kattela, Vadia Nasir, Menon Soumya V, Panigrahi Rajashree, Bushi Ganesh, Singh Mahendra, Sah Sanjit, Turkar Awakash, Goh Khang Wen, Rao S Govinda, Mawejje Edward

机构信息

Department of Pharmacy Practice, Faculty of Pharmacy, MS Ramaiah University of Applied Sciences, Bangalore, India.

Department of Pharmacy Practice, National Institute of Pharmaceutical Education and Research, Guwahati, India.

出版信息

J Diabetes Investig. 2025 Sep;16(9):1670-1682. doi: 10.1111/jdi.70111. Epub 2025 Jul 2.

Abstract

BACKGROUND

Chronic obstructive pulmonary disease (COPD) and Type 2 diabetes mellitus (T2DM) frequently coexist, amplifying morbidity, mortality, and healthcare costs. COPD exacerbations are more frequent and severe in T2DM patients, necessitating therapies addressing both conditions. This systematic review and meta-analysis evaluates the impact of sodium-glucose cotransporter-2 inhibitors (SGLT-2i) on COPD exacerbations in T2DM patients.

METHODS

Following PRISMA guidelines, we searched PubMed, Embase, and Web of Science until March 2025 for studies assessing SGLT-2i effects on COPD exacerbations in T2DM. Eligible studies included adults with T2DM-COPD overlap, reporting exacerbation outcomes. A random-effects meta-analysis and Bayesian hierarchical models were employed, with sensitivity and subgroup analyses.

RESULTS

Seven studies (449,530 participants) were included. SGLT-2i use reduced COPD exacerbation risk by 39% (pooled HR: 0.609, 95% CI: 0.431-0.858), with Bayesian analysis supporting a 31% reduction (HR: 0.64, 95% CrI: 0.40-0.88). Subgroup analyses showed superior efficacy vs DPP-4 inhibitors (HR: 0.618, 95% CI: 0.462-0.827) and sulfonylureas (HR: 0.620, 95% CI: 0.526-0.731), and modest benefit over GLP-1RAs (HR: 0.940, 95% CI: 0.890-0.992). Severe exacerbation reduction was non-significant (HR: 0.676, 95% CI: 0.340-1.344). Heterogeneity was high (I ≥ 97.9%), but sensitivity analyses confirmed robustness.

CONCLUSIONS

SGLT-2 inhibitors significantly reduce COPD exacerbations in T2DM patients, offering dual cardiometabolic and respiratory benefits. Their superiority over other antidiabetic agents supports prioritization in high-risk T2DM-COPD populations. Further trials are needed to validate effects on severe exacerbations and elucidate mechanisms.

摘要

背景

慢性阻塞性肺疾病(COPD)与2型糖尿病(T2DM)常并存,增加了发病率、死亡率和医疗成本。T2DM患者的COPD急性加重更为频繁和严重,因此需要针对这两种疾病的治疗方法。本系统评价和荟萃分析评估了钠-葡萄糖协同转运蛋白2抑制剂(SGLT-2i)对T2DM患者COPD急性加重的影响。

方法

按照PRISMA指南,我们检索了PubMed、Embase和Web of Science,直至2025年3月,以查找评估SGLT-2i对T2DM患者COPD急性加重影响的研究。符合条件的研究包括患有T2DM-COPD重叠的成年人,并报告了急性加重的结果。采用随机效应荟萃分析和贝叶斯分层模型,并进行敏感性和亚组分析。

结果

纳入了7项研究(449,530名参与者)。使用SGLT-2i可使COPD急性加重风险降低39%(合并HR:0.609,95%CI:0.431-0.858),贝叶斯分析支持降低31%(HR:0.64,95%CrI:0.40-0.88)。亚组分析显示,与二肽基肽酶4抑制剂(HR:0.618,95%CI:0.462-0.827)和磺脲类药物(HR:0.620,95%CI:0.526-0.731)相比,SGLT-2i疗效更佳,且比胰高血糖素样肽1受体激动剂(GLP-1RAs)有适度益处(HR:0.940,95%CI:0.890-0.992)。严重急性加重的减少无统计学意义(HR:0.676,95%CI:

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a061/12400361/9b49dc1bd5ee/JDI-16-1670-g005.jpg

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