Mortality and cardiovascular events in diabetes mellitus patients at dialysis initiation treated with glucagon-like peptide-1 receptor agonists.

IF 8.5 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS Cardiovascular Diabetology Pub Date : 2024-07-29 DOI:10.1186/s12933-024-02364-2
Hsuan-Wen Lai, Chun Yin See, Jui-Yi Chen, Vin-Cent Wu
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Abstract

Background: Glucagon-like Peptide-1 Receptor Agonists (GLP-1RAs) have demonstrated efficacy in improving mortality and cardiovascular (CV) outcomes. However, the impact of GLP-1RAs therapy on cardiorenal outcomes of diabetic patients at the commencement of dialysis remains unexplored.

Purpose: This study aimed to investigate the long-term benefits of GLP-1RAs in type 2 diabetic patients at dialysis commencement.

Methods: A cohort of type 2 diabetic patients initializing dialysis was identified from the TriNetX global database. Patients treated with GLP-1RAs and those treated with long-acting insulin (LAI) were matched by propensity score. We focused on all-cause mortality, four-point major adverse cardiovascular events (4p-MACE), and major adverse kidney events (MAKE).

Results: Among 82,041 type 2 diabetic patients initializing dialysis, 2.1% (n = 1685) patients were GLP-1RAs users (mean ages 59.3 years; 55.4% male). 1682 patients were included in the propensity-matched group, treated either with GLP-1RAs or LAI. The main causes of acute dialysis in this study were ischemic heart disease (17.2%), followed by heart failure (13.6%) and sepsis (6.5%). Following a median follow-up of 1.4 years, GLP-1RAs uses at dialysis commencement was associated with a reduced risk of mortality (hazard ratio [HR] = 0.63, p < 0.001), 4p-MACE (HR = 0.65, p < 0.001), and MAKE (HR = 0.75, p < 0.001). This association was particularly notable in long-acting GLP-1RAs users, with higher BMI, lower HbA1c, and those with eGFR > 15 ml/min/1.73m2. GLP-1RAs' new use at dialysis commencement was significantly associated with a lower risk of MACE (p = 0.047) and MAKE (p = 0.004). Additionally, GLP-1RAs use among those who could discontinue from acute dialysis or long-term RAs users was associated with a lower risk of mortality, 4p-MACE, and MAKE.

Conclusion: Given to the limitations of this observational study, use of GLP-1RAs at the onset of dialysis was associated with a decreased risk of MACE, MAKE, and all-cause mortality. These findings show the lack of harm associated with the use of GLP-1RAs in diabetic patients at the initiation of acute dialysis.

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开始透析时接受胰高血糖素样肽-1 受体激动剂治疗的糖尿病患者的死亡率和心血管事件。
背景:胰高血糖素样肽-1受体激动剂(GLP-1RAs)在改善死亡率和心血管(CV)预后方面具有疗效。目的:本研究旨在调查 GLP-1RAs 对开始透析的 2 型糖尿病患者的长期益处:方法:从 TriNetX 全球数据库中确定了一批开始透析的 2 型糖尿病患者。接受 GLP-1RAs 治疗的患者与接受长效胰岛素 (LAI) 治疗的患者通过倾向评分进行匹配。我们重点研究了全因死亡率、四点主要不良心血管事件(4p-MACE)和主要不良肾脏事件(MAKE):在 82041 名开始透析的 2 型糖尿病患者中,2.1%(n = 1685)的患者使用 GLP-1RAs(平均年龄 59.3 岁;55.4% 为男性)。1682名患者被纳入倾向匹配组,接受GLP-1RAs或LAI治疗。在这项研究中,急性透析的主要原因是缺血性心脏病(17.2%),其次是心力衰竭(13.6%)和败血症(6.5%)。中位随访 1.4 年后,开始透析时使用 GLP-1RAs 与死亡风险降低有关(危险比 [HR] = 0.63,p 15 ml/min/1.73m2)。透析开始时新使用 GLP-1RAs 与 MACE(p = 0.047)和 MAKE(p = 0.004)风险降低有显著相关性。此外,可以停止急性透析或长期使用 RAs 的患者使用 GLP-1RAs 与较低的死亡率、4p-MACE 和 MAKE 风险相关:鉴于这项观察性研究的局限性,在开始透析时使用 GLP-1RAs 与 MACE、MAKE 和全因死亡风险降低有关。这些研究结果表明,糖尿病患者在急性透析开始时使用 GLP-1RAs 不会造成危害。
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来源期刊
Cardiovascular Diabetology
Cardiovascular Diabetology 医学-内分泌学与代谢
CiteScore
12.30
自引率
15.10%
发文量
240
审稿时长
1 months
期刊介绍: Cardiovascular Diabetology is a journal that welcomes manuscripts exploring various aspects of the relationship between diabetes, cardiovascular health, and the metabolic syndrome. We invite submissions related to clinical studies, genetic investigations, experimental research, pharmacological studies, epidemiological analyses, and molecular biology research in this field.
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