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二肽基肽酶4抑制剂对2型糖尿病肾病患者心血管事件的影响:一项系统评价和荟萃分析

Effect of Dipeptidyl Peptidase 4 Inhibitors on Cardiovascular Events in Type-2 Diabetes Patients with Renal Impairment: A Systematic Review and Meta-analysis.

作者信息

Khalse Maneesha, Ganapathy B

机构信息

Department of Medical Affairs, Lupin limited, Mumbai, Maharashtra, India.

Department Of Endocrinology, St. John's Medical College and Hospital, Bangalore, Karnataka, India.

出版信息

Indian J Endocrinol Metab. 2020 Mar-Apr;24(2):143-149. doi: 10.4103/ijem.IJEM_568_19. Epub 2020 Apr 30.

DOI:10.4103/ijem.IJEM_568_19
PMID:32699780
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7333763/
Abstract

BACKGROUND

Recent studies suggested that the increased risk of heart failure by DPP-4 inhibitors may have an interconnection with patients' baseline eGFR. We decided to investigate the effect of DPP-4 inhibitors and the degree of renal function on cardiovascular (CV) safety in type 2 diabetes (T2D) patients.

MATERIALS AND METHODS

Systemic search of literature that examined the DPP-4 inhibitors and reported cardiovascular outcomes in diabetes patients with renal impairment were performed. Studies were examined for inclusion criteria: Randomized controlled trials with reduced renal function taking DPP-4 inhibitors alone or in combination with other anti-diabetes agents reporting evaluable CV events for at least 24 weeks.

RESULT

Analysis of four CV outcome studies (11,789 patients with eGFR ≤60 ml/min/1.73m) did not find any increase in primary composite endpoints with DPP-4 inhibitors in patients stratified by baseline renal function. Rate of hospitalization due to heart failure (hHF) is found to be non-inferior to placebo group in patients with renal insufficiency (RR 1.07; 95% CI, 0.96-1.20 = 0.26). In moderate renal dysfunction, there is a significant increase in heart failure risk compared to placebo. (RR 1.27; 95% CI, 1.033 -1.5 8; = 0.024).

CONCLUSION

Treatment with DPP-4 inhibitors did not affect the risk of cardiovascular events regardless of baseline renal function, however, an increase in the risk of hHF in moderate renal function in T2D patients with high CV risk merits careful consideration. Further research would be necessitated to reach definitive conclusion to understand the effect of declining renal function on CV safety of DPP-4 inhibitors.

摘要

背景

近期研究表明,二肽基肽酶-4(DPP-4)抑制剂导致心力衰竭风险增加可能与患者的基线估算肾小球滤过率(eGFR)有关。我们决定研究DPP-4抑制剂的作用以及肾功能程度对2型糖尿病(T2D)患者心血管(CV)安全性的影响。

材料与方法

对研究DPP-4抑制剂并报告糖尿病肾功能损害患者心血管结局的文献进行系统检索。审查研究的纳入标准:肾功能降低的随机对照试验,单独使用DPP-4抑制剂或与其他抗糖尿病药物联合使用,报告至少24周的可评估CV事件。

结果

对四项CV结局研究(11789例eGFR≤60 ml/min/1.73m²的患者)进行分析,发现在按基线肾功能分层的患者中,DPP-4抑制剂并未使主要复合终点增加。在肾功能不全的患者中,因心力衰竭住院率(hHF)不劣于安慰剂组(风险比[RR] 1.07;95%置信区间[CI],0.96 - 1.20;P = 0.26)。与安慰剂相比,中度肾功能不全时心力衰竭风险显著增加(RR 1.27;95% CI,1.033 - 1.58;P = 0.024)。

结论

无论基线肾功能如何,使用DPP-4抑制剂治疗均不影响心血管事件风险,然而,高CV风险的T2D患者中度肾功能不全时hHF风险增加值得仔细考虑。需要进一步研究以得出明确结论,了解肾功能下降对DPP-4抑制剂CV安全性的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8216/7333763/f249c478e31f/IJEM-24-143-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8216/7333763/eef8d054b287/IJEM-24-143-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8216/7333763/2cd28996adc6/IJEM-24-143-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8216/7333763/3ca761fc9f05/IJEM-24-143-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8216/7333763/f249c478e31f/IJEM-24-143-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8216/7333763/eef8d054b287/IJEM-24-143-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8216/7333763/2cd28996adc6/IJEM-24-143-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8216/7333763/3ca761fc9f05/IJEM-24-143-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8216/7333763/f249c478e31f/IJEM-24-143-g004.jpg

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Linagliptin Effects on Heart Failure and Related Outcomes in Individuals With Type 2 Diabetes Mellitus at High Cardiovascular and Renal Risk in CARMELINA.卡格列净对伴有高心血管和肾脏风险的 2 型糖尿病患者的心力衰竭和相关结局的影响:CARMELINA 研究。
Circulation. 2019 Jan 15;139(3):351-361. doi: 10.1161/CIRCULATIONAHA.118.038352.
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Effect of Linagliptin vs Placebo on Major Cardiovascular Events in Adults With Type 2 Diabetes and High Cardiovascular and Renal Risk: The CARMELINA Randomized Clinical Trial.
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Dipeptidyl peptidase-4 independent cardiac dysfunction links saxagliptin to heart failure.二肽基肽酶-4非依赖性心脏功能障碍将沙格列汀与心力衰竭联系起来。
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