2型糖尿病患者基线血糖状态与新抗糖尿病药物治疗前后芬尼酮的心血管结局

Endocrinology and metabolism (Seoul, Korea) Pub Date : 2022-02-01 Epub Date: 2022-02-09 DOI:10.3803/EnM.2021.1296
Dimitrios Patoulias, Christodoulos Papadopoulos, Asterios Karagiannis, Vassilios Vassilikos, Michael Doumas
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引用次数: 2

摘要

2型糖尿病(T2DM)与心血管疾病密切相关。我们试图根据先前使用新的抗糖尿病药物和血糖状态来确定芬烯酮的心脏保护作用。我们检索了PubMed和Cochrane图书馆从成立到2021年10月1日的随机对照试验(rct),以评估芬尼酮对T2DM患者主要不良心血管结局的影响。我们将主要终点定为主要心血管不良事件(MACE),定义为心血管原因死亡、非致死性心肌梗死、非致死性中风或因心力衰竭住院的综合死亡。我们最终在定量综合中纳入了两项随机对照试验。与安慰剂相比,芬尼酮诱导复合心血管终点风险降低23%,无论先前的血糖水平如何。我们还发现,与安慰剂相比,芬尼酮对肥胖T2DM患者的心血管有显著益处,尽管这种益处在体重指数低于30 kg/m2的受试者中有所减弱。最后,细芬烯酮与钠-葡萄糖共转运蛋白-2抑制剂或胰高血糖素样肽-1受体激动剂联合使用并没有显著降低MACE的风险。我们得出结论,细芬烯酮对2型糖尿病患者的心血管有显著的益处,尤其是对那些肥胖的患者,而血糖水平或在基线时使用较新的抗糖尿病药物治疗并不影响观察到的心脏保护作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cardiovascular Outcomes with Finerenone According to Glycemic Status at Baseline and Prior Treatment with Newer Antidiabetics among Patients with Type 2 Diabetes Mellitus.

Cardiovascular Outcomes with Finerenone According to Glycemic Status at Baseline and Prior Treatment with Newer Antidiabetics among Patients with Type 2 Diabetes Mellitus.

Type 2 diabetes mellitus (T2DM) and cardiovascular disease are closely interconnected. We sought to determine the cardioprotective action of finerenone according to prior treatment with newer antidiabetics and glycemic status. We searched PubMed and Cochrane Library from inception to October 1, 2021 for randomized controlled trials (RCTs) assessing the effect of finerenone on major adverse cardiovascular outcomes in patients with T2DM. We set the primary endpoint as major adverse cardiovascular events (MACE), defined as the composite of death from cardiovascular causes, nonfatal myocardial infarction, nonfatal stroke, or hospitalization for heart failure. We finally included two RCTs in our quantitative synthesis. Compared to placebo, finerenone induced a 23% risk reduction for the composite cardiovascular endpoint, regardless of prior glycemia. We also showed that finerenone provided significant cardiovascular benefit for obese patients with T2DM compared to placebo, although this benefit was diminished for subjects with a body mass index lower than 30 kg/m2. Finally, the combination of finerenone with sodium-glucose co-transporter-2 inhibitors or glucagon-like peptide-1 receptor agonists did not produce a significant risk reduction for MACE. We conclude that finerenone provides significant cardiovascular benefits for patients with T2DM, especially for those who are obese, while glycemic status or treatment with newer antidiabetics at baseline does not affect the observed cardioprotective action.

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