Department of Pharmacy, Tongji Hospital, School of Medicine, Tongji University, Shanghai, China.
Department of Pharmacy, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Front Endocrinol (Lausanne). 2023 Jul 3;14:1203666. doi: 10.3389/fendo.2023.1203666. eCollection 2023.
Sarcopenia has been recognized as the third category of disabling complications in patients with type 2 diabetes mellitus(T2DM), in addition to micro- and macrovascular complications. Sodium-glucose co-transporter 2 (SGLT2) inhibitors are innovative glucose-lowering treatments that have been shown to reduce body weight and enhance cardiovascular and renal outcomes. However, there is vigilance that SGLT2 inhibitors should be taken cautiously because they target skeletal muscle and may raise the risk of sarcopenia. Herein, we conducted a meta-analysis of randomized controlled trials to evaluate the effects of SGLT2 inhibitors on sarcopenia in patients with T2DM.
Relevant studies were obtained from PubMed, Embase, Medicine, Cochrane, and Web of Science databases to determine eligible studies until February 2023, without any language restrictions. A random effects model was utilized irrespective of heterogeneity, and the I statistic was used to evaluate study heterogeneity. The differences in results were measured using the weighted average difference (WMD) of the continuous data, along with a 95% confidence interval (CI).
A total of 25 randomized controlled trials with 2,286 participants were included. SGLT2 inhibitors significantly reduced weight-related changes and fat-related changes, including body weight(BW) (WMD= -2.74, 95% CI: -3.26 to -2.23, P<0.01), body mass index(BMI) (WMD= -0.72, 95% CI: -0.95 to -0.49, P<0.01), waist circumference(WC) (WMD= -1.60, 95% CI: -2.99 to -0.22, P=0.02), fat mass(FM)(WMD= -1.49, 95% CI: -2.18 to -0.80, P<0.01), percentage body fat(PBF) (WMD= -1.28, 95% CI: -1.83 to -0.74, P<0.01), visceral fat area(VFA)(WMD= -19.52, 95% CI: -25.90 to -13.14, P<0.01), subcutaneous fat area(SFA)(WMD= -19.11, 95% CI: -31.18 to -7.03, P=0.002), In terms of muscle-related changes, lean mass(LM)(WMD= -0.80, 95% CI: -1.43 to -0.16, P=0.01), and skeletal muscle mass(SMM) (WMD= -0.38, 95% CI: -0.65 to -0.10, P=0.007), skeletal muscle index(SMI) (WMD= -0.12, 95% CI: -0.22 to -0.02, P=0.02)were also significantly reduced. In addition, body water likewise decreased significantly (WMD=-0.96, 95% CI: -1.68 to -0.23, P=0.009).
As one of the most widely used hypoglycemic, SGLT2 inhibitors have beneficial effects on FM and BW weight loss in T2DM, such as BW, BMI, WC, FM, PBF, VFA, and SFA. However, the negative influence on muscle mass paralleled the reduction in FM and BW, and the consequent increased risk of sarcopenia warrants high attention, especially as patients are already predisposed to physical frailty.
https://www.crd.york.ac.uk/prospero/#myprospero, identifier PROSPERO (No.CRD 42023396278).
肌少症已被认为是 2 型糖尿病(T2DM)患者除微血管和大血管并发症之外的第三类致残性并发症。钠-葡萄糖共转运蛋白 2(SGLT2)抑制剂是一种创新的降糖治疗方法,已被证明可降低体重并改善心血管和肾脏结局。然而,有人担心 SGLT2 抑制剂应该谨慎使用,因为它们针对骨骼肌,并可能增加肌少症的风险。在此,我们进行了一项荟萃分析,以评估 SGLT2 抑制剂对 T2DM 患者肌少症的影响。
从 PubMed、Embase、Medicine、Cochrane 和 Web of Science 数据库中获取相关研究,以确定符合条件的研究,截至 2023 年 2 月,不限制任何语言。无论是否存在异质性,均采用随机效应模型进行分析,使用 I 统计量评估研究异质性。使用连续数据的加权平均差异(WMD)和 95%置信区间(CI)来衡量结果的差异。
共纳入 25 项随机对照试验,涉及 2286 名参与者。SGLT2 抑制剂显著降低了体重相关变化和脂肪相关变化,包括体重(BW)(WMD=-2.74,95%CI:-3.26 至-2.23,P<0.01)、体重指数(BMI)(WMD=-0.72,95%CI:-0.95 至-0.49,P<0.01)、腰围(WC)(WMD=-1.60,95%CI:-2.99 至-0.22,P=0.02)、脂肪量(FM)(WMD=-1.49,95%CI:-2.18 至-0.80,P<0.01)、体脂百分比(PBF)(WMD=-1.28,95%CI:-1.83 至-0.74,P<0.01)、内脏脂肪面积(VFA)(WMD=-19.52,95%CI:-25.90 至-13.14,P<0.01)、皮下脂肪面积(SFA)(WMD=-19.11,95%CI:-31.18 至-7.03,P=0.002)。在肌肉相关变化方面,瘦体重(LM)(WMD=-0.80,95%CI:-1.43 至-0.16,P=0.01)和骨骼肌量(SMM)(WMD=-0.38,95%CI:-0.65 至-0.10,P=0.007)以及骨骼肌指数(SMI)(WMD=-0.12,95%CI:-0.22 至-0.02,P=0.02)也显著降低。此外,身体水分也显著减少(WMD=-0.96,95%CI:-1.68 至-0.23,P=0.009)。
作为最广泛使用的降糖药物之一,SGLT2 抑制剂对 T2DM 患者的 FM 和 BW 体重减轻具有有益作用,例如 BW、BMI、WC、FM、PBF、VFA 和 SFA。然而,肌肉质量的负面影响与 FM 和 BW 的减少相平行,随之增加的肌少症风险需要高度关注,尤其是在患者已经存在身体虚弱的情况下。
https://www.crd.york.ac.uk/prospero/#myprospero,标识符 PROSPERO(无.CRD 42023396278)。