Chai Shang-Yu, Zhang Ru-Ya, Ning Zhi-Yuan, Zheng Yi-Man, Swapnil Rajpathak, Ji Li-Nong
Value and Implementation Global Medical and Scientific Affairs, MSD China, Shanghai 200030, China.
Value and Implementation Outcomes Research, MRL, Merck and Co., Inc., Rahway, NJ 19454, United States.
World J Diabetes. 2025 Jul 15;16(7):107335. doi: 10.4239/wjd.v16.i7.107335.
Sodium-glucose cotransporter 2 (SGLT2) inhibitors are widely used for the treatment of type 2 diabetes (T2D).
To evaluate the influence of SGLT2 inhibitors on homeostasis model assessment of insulin resistance (HOMA-IR) and β-cell function (HOMA-β) in patients with T2D in a meta-analysis.
Randomized controlled trials (RCTs) comparing SGLT2 inhibitors to placebo in T2D patients, with a minimum treatment duration of 12 weeks, were searched using the PubMed, EMBASE, and Cochrane Library databases. Risk of bias was assessed using the Cochrane Risk of Bias Tool, and the certainty of evidence was evaluated using the Grading of Recommendations, Assessment, Development and Evaluation (GRADE) system. Changes in HOMA-IR and HOMA-β were the outcomes analyzed. Meta-analyses were performed using a random-effects model by incorporating the potential influences of heterogeneity.
Of 1388 articles identified, 24 RCTs met the inclusion criteria. 23 of the included studies were double-blind RCTs with low risk of bias. Pooled results including 2272 patients showed that SGLT2 inhibitors significantly reduced HOMA-IR compared to placebo [mean difference (MD) = -0.81, 95% confidence interval (CI): -1.11 to -0.52, < 0.001; = 82%], indicating reduced insulin resistance. Additionally, meta-analysis with 2845 patients suggested that SGLT2 inhibitors significantly increased HOMA-β (MD = 7.90, 95%CI: 5.44-10.37, < 0.001; = 74%) compared to placebo in patients with T2D, indicating improved β-cell function. Based on GRADE assessment, the certainty of evidence was rated moderate for both outcomes due to heterogeneity. Subgroup analyses showed that HOMA-β increased more substantially in non-Asian studies than in Asian studies ( for subgroup difference < 0.01). Subgroup analyses according to the individual medications of SGLT2 inhibitors all showed significant improvement of HOMA-IR and HOMA-β ( all < 0.05). No significant publication bias was detected ( for Egger's test all > 0.05).
SGLT2 inhibitors are associated with improvements in insulin resistance and β-cell function in patients with T2D, although the certainty of evidence is moderate due to heterogeneity.
钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂被广泛用于治疗2型糖尿病(T2D)。
通过一项荟萃分析评估SGLT2抑制剂对T2D患者胰岛素抵抗稳态模型评估(HOMA-IR)和β细胞功能(HOMA-β)的影响。
使用PubMed、EMBASE和Cochrane图书馆数据库检索比较SGLT2抑制剂与安慰剂治疗T2D患者且最短治疗持续时间为12周的随机对照试验(RCT)。使用Cochrane偏倚风险工具评估偏倚风险,并使用推荐分级、评估、制定与评价(GRADE)系统评估证据的确定性。分析的结局指标为HOMA-IR和HOMA-β的变化。通过纳入异质性的潜在影响,采用随机效应模型进行荟萃分析。
在检索到的1388篇文章中,24项RCT符合纳入标准。纳入的研究中有23项为双盲RCT,偏倚风险低。纳入2272例患者的汇总结果显示,与安慰剂相比,SGLT2抑制剂显著降低了HOMA-IR[平均差(MD)=-0.81,95%置信区间(CI):-1.11至-0.52,P<0.001;I²=82%],表明胰岛素抵抗降低。此外,纳入2845例患者的荟萃分析表明,与安慰剂相比,SGLT2抑制剂在T2D患者中显著增加了HOMA-β(MD=7.90,95%CI:5.44-10.37,P<0.001;I²=74%),表明β细胞功能改善。基于GRADE评估,由于存在异质性,两个结局指标的证据确定性均被评为中等。亚组分析显示,非亚洲研究中HOMA-β的增加幅度大于亚洲研究(亚组差异P<0.01)。根据SGLT2抑制剂的个体药物进行的亚组分析均显示HOMA-IR和HOMA-β有显著改善(所有P<0.05)。未检测到显著的发表偏倚(Egger检验所有P>0.05)。
SGLT2抑制剂与T2D患者胰岛素抵抗和β细胞功能的改善相关,尽管由于异质性证据确定性为中等。