Centre for Clinical Epidemiology, Lady Davis Institute, Jewish General Hospital, Montreal, Quebec, Canada Division of Endocrinology, Jewish General Hospital, Montreal, Quebec, Canada.
Centre for Clinical Epidemiology, Lady Davis Institute, Jewish General Hospital, Montreal, Quebec, Canada Department of Epidemiology, Biostatistics, and Occupational Health, McGill University, Montreal, Quebec, Canada Division of Clinical Epidemiology, Department of Medicine, McGill University, Montreal, Quebec, Canada.
Diabetes Care. 2015 Feb;38(2):277-84. doi: 10.2337/dc14-1459. Epub 2014 Sep 9.
To determine whether the use of incretin-based drugs, including GLP-1 analogs and dipeptidyl peptidase-4 inhibitors, is associated with an increased risk of congestive heart failure (CHF) among patients with type 2 diabetes.
The U.K. Clinical Practice Research Datalink, linked to the Hospital Episode Statistics database, was used to conduct a cohort study with a nested case-control analysis among patients newly prescribed antidiabetic drugs between 1 January 2007 and 31 March 2012 and no prior history of CHF. Case subjects were defined as patients hospitalized for a first CHF and matched with up to 20 control subjects on age, duration of treated diabetes, calendar year, and time since cohort entry. Conditional logistic regression was used to estimate odds ratios (ORs) with corresponding 95% CIs of incident CHF comparing current use of incretin-based drugs with current use of two or more oral antidiabetic drugs.
The cohort consisted of 57,737 patients followed for a mean 2.4 years, during which time 1,118 incident cases of hospitalized CHF were identified (incidence rate 8.1/1,000 person-years). Current use of incretin-based drugs was not associated with an increased risk of CHF (adjusted OR 0.85 [95% CI 0.62-1.16]). Secondary analyses revealed no duration-response relationship (P trend = 0.39).
In our population-based study, incretin-based drug use was not associated with an increased risk of CHF among patients with type 2 diabetes. These findings provide some reassurance, but will need to be replicated in other large-scale studies.
确定肠促胰岛素类药物(包括 GLP-1 类似物和二肽基肽酶-4 抑制剂)的使用是否与 2 型糖尿病患者充血性心力衰竭(CHF)风险增加相关。
利用英国临床实践研究数据链接(与医院发病统计数据库相关联),开展了一项队列研究,对 2007 年 1 月 1 日至 2012 年 3 月 31 日期间新处方抗糖尿病药物且无 CHF 既往史的患者进行了嵌套病例对照分析。病例组定义为因首次 CHF 住院的患者,并按年龄、糖尿病治疗时间、日历年份和队列入组时间与最多 20 名对照患者进行匹配。采用条件逻辑回归比较肠促胰岛素类药物的当前使用与两种或更多口服抗糖尿病药物的当前使用,估计 CHF 发生率的比值比(OR)及其相应的 95%置信区间(CI)。
该队列包括 57737 名患者,平均随访 2.4 年,在此期间,确定了 1118 例住院 CHF 事件(发生率为 8.1/1000 人年)。肠促胰岛素类药物的当前使用与 CHF 风险增加无关(调整后 OR 0.85 [95%CI 0.62-1.16])。二次分析显示无持续时间-反应关系(P 趋势=0.39)。
在我们的基于人群的研究中,肠促胰岛素类药物的使用与 2 型糖尿病患者的 CHF 风险增加无关。这些发现提供了一些保证,但需要在其他大规模研究中进行复制。