Sodium-glucose co-transporter 2 inhibitors (SGLT2i); as a preventive factor of kidney failure in patients with type 2 diabetes; a meta-analysis of randomized controlled trials

IF 0.2 Q4 UROLOGY & NEPHROLOGY Journal of Renal Injury Prevention Pub Date : 2021-09-09 DOI:10.34172/jrip.2021.35
Dorsa Jahangiri, Udit Narayan Padhi, H. Verma, B. Lakkakula, R. Valizadeh, H. Nasri
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引用次数: 2

Abstract

Introduction: Sodium-glucose co-transporter 2 inhibitors (SGLT2i) are a new class of anti-diabetic drugs. SGLT2 inhibitors lower blood glucose levels by decreasing glucose reabsorption in the proximal renal tubule, resulting in increased urinary glucose and sodium excretion. Objective: This study was conducted to investigate the effects of SGLT2i on individual renal outcomes in diabetic patients. Methods: This study was a systematic review and meta-analysis of clinical trials. A comprehensive search of Cochrane Central Register of Controlled Trials was conducted in the Cochrane Library and PubMed, to identify relevant articles focusing on SGLT2i and chronic kidney disease (CKD) in diabetic patients. The most recent article search was conducted on July 12, 2021. Results: Seven randomized controlled trials (RCTs) were included in the meta-analysis. Two trials were comparing dapagliflozin, two comparing empagliflozin, one comparing ertugliflozin, one comparing canagliflozin, and one comparing sotagliflozin. Composite renal outcome and acute kidney injury (AKI) was found in seven and four studies, respectively. Data on end-stage kidney disease (ESKD) and albuminuria or initiation of renal replacement therapy were reported in the two studies. The pooled risk ratio (RR) 95% confidence interval (CI) for the composite renal outcome was 0.54 (0.50–0.59), with 92 % heterogeneity. The pooled RR for AKI was 0.77 (0.66–0.89), with no heterogeneity. A significant lower incidence of albuminuria (RR: 0.69; 95% CI: 0.59–0.81), initiation of renal replacement therapy (RR: 0.71; 95% CI: 0.58–0.87), was observed following the use of SGLT2 inhibitors. Conclusion: Our findings confirm that the SGLT2 inhibitors can reduce the risk of albuminuria, AKI and renal replacement therapy in ESKD patients with T2D (type 2 diabetes). These meta-analyses provide substantial evidence supporting the beneficial effect of SGLT2 inhibitors on reducing CKD events in individuals with T2D.
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钠-葡萄糖共转运蛋白2抑制剂(SGLT2i);作为2型糖尿病患者肾功能衰竭的预防因素;随机对照试验的荟萃分析
钠-葡萄糖共转运蛋白2抑制剂(SGLT2i)是一类新型的抗糖尿病药物。SGLT2抑制剂通过减少近端肾小管的葡萄糖重吸收来降低血糖水平,导致尿糖和钠排泄增加。目的:本研究旨在探讨SGLT2i对糖尿病患者个体肾脏预后的影响。方法:本研究采用临床试验的系统综述和荟萃分析。我们在Cochrane图书馆和PubMed中对Cochrane中央对照试验注册库进行了全面检索,以确定关注糖尿病患者SGLT2i和慢性肾脏疾病(CKD)的相关文章。最近的文章搜索是在2021年7月12日进行的。结果:meta分析纳入了7项随机对照试验(RCTs)。两项试验比较达格列净,两项比较恩格列净,一项比较埃图格列净,一项比较卡格列净,一项比较索他列净。复合肾结局和急性肾损伤(AKI)分别在7项和4项研究中发现。这两项研究报告了终末期肾病(ESKD)和蛋白尿或开始肾脏替代治疗的数据。综合肾脏结局的合并风险比(RR) 95%可信区间(CI)为0.54(0.50-0.59),异质性为92%。AKI的合并RR为0.77(0.66-0.89),无异质性。蛋白尿发生率显著降低(RR: 0.69;95% CI: 0.59-0.81),开始肾脏替代治疗(RR: 0.71;95% CI: 0.58-0.87),在使用SGLT2抑制剂后观察到。结论:我们的研究结果证实,SGLT2抑制剂可以降低ESKD合并T2D(2型糖尿病)患者蛋白尿、AKI和肾脏替代治疗的风险。这些荟萃分析提供了大量证据,支持SGLT2抑制剂对减少T2D患者CKD事件的有益作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Renal Injury Prevention
Journal of Renal Injury Prevention UROLOGY & NEPHROLOGY-
CiteScore
1.60
自引率
0.00%
发文量
36
期刊介绍: The Journal of Renal Injury Prevention (JRIP) is a quarterly peer-reviewed international journal devoted to the promotion of early diagnosis and prevention of renal diseases. It publishes in March, June, September and December of each year. It has pursued this aim through publishing editorials, original research articles, reviews, mini-reviews, commentaries, letters to the editor, hypothesis, case reports, epidemiology and prevention, news and views and renal biopsy teaching point. In this journal, particular emphasis is given to research, both experimental and clinical, aimed at protection/prevention of renal failure and modalities in the treatment of diabetic nephropathy. A further aim of this journal is to emphasize and strengthen the link between renal pathologists/nephropathologists and nephrologists. In addition, JRIP welcomes basic biomedical as well as pharmaceutical scientific research applied to clinical nephrology. Futuristic conceptual hypothesis that integrate various fields of acute kidney injury and renal tubular cell protection are encouraged to be submitted.
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