A systematic review of sodium-glucose cotransporter 2 inhibitors and renal profiles among Japanese patients with type 2 diabetes mellitus.

IF 1.2 Q4 PHARMACOLOGY & PHARMACY
Junichi Mukai, Nakaba Okamura, Yuki Saito, Rie Kubota
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Abstract

Background: We conducted a systematic review and meta-analysis to summarize the available literature and comprehensively appraise the renal profiles of sodium-glucose cotransporter 2 inhibitors (SGLT2i) in Japanese patients with type 2 diabetes mellitus (T2DM).

Methods: The electronic databases MEDLINE, Ichushi-web, and ClinicalTrials.gov were searched for studies without language restrictions from their inception until 20 July 2023 and CENTRAL until 21 September 2021. Studies were included if they were double-masked randomized controlled trials (RCTs) (1) including Japanese patients with T2DM aged > 18 years who received SGLT2i or a placebo, (2) reporting at least one renal outcome of serum creatinine or the estimated glomerular filtration rate (eGFR), and (3) with a follow-up of > 12 weeks. Cross-over and open label trials were excluded. The risk of bias based on the Cochrane risk-of-bias tool for randomized trials (RoB 2) was appraised. We computed the weighed mean difference with 95%CI for each renal outcome and used a random-effects model (inverse variance method).

Results: We ultimately retrieved 13 RCTs including 2687 individuals in our review. The durations of RCTs ranged between 12 and 104 weeks. Only one trial had a longer duration of more than one year. Ten out of 13 RCTs reported serum creatinine, while nine included eGFR. Serum creatinine and eGFR were slightly worse with SGLT2i than with a placebo [mean difference 0.01 (95%CI 0.00 to 0.02) mg/dL, p = 0.002, mean difference - 1.30 (95%CI -2.23 to -0.37) mL/min/1.73 m2, p = 0.006, respectively]. Merged results revealed insignificant heterogeneity (I2 < 30%).

Conclusion: These results suggest that SGLT2i slightly worsens serum creatinine and eGFR in Japanese patients with T2DM. However, since the durations of most RCTs were short, the effects of eGFR in particular may be transient. Further evidence is needed from rigorous studies that focus on renal outcomes with a longer duration to confirm the present results.

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日本2型糖尿病患者钠-葡萄糖共转运蛋白2抑制剂和肾脏特征的系统综述
背景:我们进行了一项系统回顾和荟萃分析,总结了现有文献,并全面评估了钠-葡萄糖共转运蛋白2抑制剂(SGLT2i)在日本2型糖尿病(T2DM)患者的肾脏状况。方法:检索MEDLINE、Ichushi-web和ClinicalTrials.gov电子数据库,检索从研究开始至2023年7月20日和CENTRAL数据库至2021年9月21日无语言限制的研究。研究纳入双盲随机对照试验(RCTs)(1),包括接受SGLT2i或安慰剂治疗的18岁日本T2DM患者,(2)报告至少一项血清肌酐或估计肾小球滤过率(eGFR)的肾脏结局,(3)随访12周。排除了交叉试验和开放标签试验。采用随机试验Cochrane风险-偏倚工具(RoB 2)评价偏倚风险。我们以95%CI计算每个肾脏结局的加权平均差,并使用随机效应模型(反方差法)。结果:我们最终检索到13项随机对照试验,包括2687名受试者。随机对照试验的持续时间为12至104周。只有一项试验的持续时间超过一年。13项随机对照试验中有10项报告了血清肌酐,9项报告了eGFR。SGLT2i组血清肌酐和eGFR略低于安慰剂组[平均差异为0.01 (95%CI 0.00 ~ 0.02) mg/dL, p = 0.002,平均差异为1.30 (95%CI -2.23 ~ -0.37) mL/min/1.73 m2, p = 0.006]。合并结果显示不明显的异质性(结论:这些结果表明SGLT2i轻微恶化日本T2DM患者的血清肌酐和eGFR。然而,由于大多数随机对照试验的持续时间较短,eGFR的影响尤其可能是短暂的。进一步的证据需要从严格的研究集中在肾脏预后与较长的持续时间来证实目前的结果。
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
CiteScore
1.80
自引率
0.00%
发文量
29
审稿时长
8 weeks
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