SGLT-2抑制剂与COPD患者COPD恶化和死亡率的风险

Fu-Shun Yen, James Cheng-Chung Wei, Yu-Han Huang, Tzu-Ju Hsu, Sing-Ting Wang, Chii-Min Hwu, Chih-Cheng Hsu
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引用次数: 0

摘要

理由:慢性阻塞性肺疾病(COPD)患者易发生急性加重、心血管疾病和过早死亡。目的:比较2型糖尿病(T2DM)和COPD患者使用和不使用钠-葡萄糖共转运蛋白-2 (SGLT-2)抑制剂之间COPD加重、心血管疾病和死亡率的风险。方法:本研究纳入2009年1月1日至2020年12月31日国家健康保险研究数据库中诊断为T2DM和COPD的299168例患者。使用Cox比例风险模型来检查SGLT-2抑制剂使用者和非使用者之间的主要不良心血管事件、COPD住院、无创正压通气(NIPPV)、有创机械通气、肺癌和死亡率的相对风险。我们使用倾向评分匹配选择1288对SGLT-2抑制剂使用者和非使用者。测量结果和主要结果:在匹配的队列中,使用SGLT-2抑制剂与未使用SGLT-2抑制剂相比,死亡率(aHR 0.64, 95% CI 0.43-0.95)、NIPPV (aHR 0.48, 95% CI 0.27-0.87)和COPD住院(aHR 0.82, 95% CI 0.69-0.98)的风险显著降低。亚组和剂量反应分析显示,SGLT-2抑制剂的使用与死亡率、NIPPV和COPD住院的风险显著降低相关(结论:这项基于人群的队列研究表明,在T2DM和COPD患者中,SGLT-2抑制剂的使用与COPD加重、呼吸机支持和死亡率的风险较低相关。SGLT-2抑制剂可能在治疗慢性阻塞性肺病和糖尿病患者中发挥作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
SGLT-2 Inhibitors and the Risk of Chronic Obstructive Pulmonary Disease Exacerbations and Mortality in Chronic Obstructive Pulmonary Disease Patients.

Rationale: Patients with chronic obstructive pulmonary disease (COPD) are susceptible to acute exacerbations, cardiovascular disease, and premature death. Objectives: To compare the risk of COPD exacerbation, cardiovascular diseases, and mortality between SGLT-2 (sodium-glucose cotransporter-2) inhibitor use and nonuse in patients with type 2 diabetes mellitus (T2DM) and COPD. Methods: The study included 299,168 patients with diagnoses of T2DM and COPD in the National Health Insurance Research Database from January 1, 2009, to December 31, 2020. Cox proportional hazards models were used to examine the relative hazard of the primary outcome (a composite of hospitalization for COPD, noninvasive positive-pressure ventilation [NIPPV], invasive mechanical ventilation, and all-cause mortality) and secondary outcomes: major adverse cardiovascular events, hospitalization for COPD, NIPPV, invasive mechanical ventilation, lung cancer, and mortality between SGLT-2 inhibitor users and nonusers. We used propensity score matching to select 1,288 pairs of SGLT-2 inhibitor users and nonusers. Results: In the matched cohorts, SGLT-2 inhibitor use was associated with a significantly lower risk of the primary outcome (multivariable-adjusted hazard ratio [aHR], 0.79 [95% confidence interval (CI), 0.67-0.93]), NIPPV (aHR, 0.48 [95% CI, 0.27-0.87]), hospitalization for COPD (aHR, 0.82 [95% CI, 0.69-0.98]), and mortality (aHR, 0.64 [95% CI, 0.43-0.95]), than SGLT-2 inhibitor nonuse. Subgroup and dose-response analyses showed that SGLT-2 inhibitor use was associated with a significantly lower risk of mortality, NIPPV, and hospitalization for COPD (P < 0.05) than nonuse of SGLT-2 inhibitors. Conclusions: This population-based cohort study showed that SGLT-2 inhibitor use was associated with a lower risk of the primary outcome, COPD exacerbations, ventilator support, and mortality than SGLT-2 inhibitor nonuse in patients with T2DM and COPD. SGLT-2 inhibitors may have a role in treating patients with COPD and diabetes.

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