Sattar Naveed, Neeland Ian J, Dahlqvist Leinhard Olof, Fernández Landó Laura, Bray Ross, Linge Jennifer, Rodriguez Angel
School of Cardiovascular and Metabolic Health, British Heart Foundation Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.
Harrington Heart and Vascular Institute, University Hospitals Cleveland Medical Center and Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.
Lancet Diabetes Endocrinol. 2025 Jun;13(6):482-493. doi: 10.1016/S2213-8587(25)00027-0. Epub 2025 Apr 30.
Substantial weight reduction is often associated with loss of muscle mass. Tirzepatide has been associated with significant reductions in body weight in type 2 diabetes trials and a beneficial effect on body fat distribution in the SURPASS-3 MRI substudy. This post-hoc exploratory analysis studied the association of tirzepatide treatment with changes in thigh muscle volume, muscle volume Z score, and muscle fat infiltration, and aimed to contextualise the results using longitudinal MRI data from UK Biobank participants.
SURPASS-3 was a randomised, open-label, parallel-group, phase 3 trial. The multicentre (45 sites) and multinational (eight countries) MRI substudy of SURPASS-3 enrolled insulin-naive adults (aged ≥18 years) with type 2 diabetes who were on treatment with metformin with or without a sodium-glucose co-transporter-2 (SGLT-2) inhibitor, had an HbA of 7·0-10·5% (53-91 mmol/mol), a BMI of at least 25 kg/m, and a fatty liver index of at least 60. Participants were randomly assigned (1:1:1:1) to receive subcutaneous injection once per week of tirzepatide (5, 10, or 15 mg), or subcutaneous injection once per day of titrated insulin degludec. Thigh muscle fat infiltration, muscle volume, and muscle volume Z score (invariant to sex, height, weight, and BMI) were quantified by MRI at baseline and week 52. In this post-hoc analysis, we assessed the differences between mean baseline and week 52 muscle composition values in the tirzepatide groups (pooled 5 mg, 10 mg, and 15 mg group, and per dose group) and insulin degludec group using paired t tests, and the differences in muscle composition changes with pooled tirzepatide versus insulin degludec via adjusted ANCOVA models. Observed changes in muscle fat infiltration, muscle volume, and muscle volume Z scores were compared using paired t tests to population-based estimates calculated from multiple linear regression models fitted to UK Biobank data (n=2942), capturing associations with change in body weight. Analyses were done by modified intention to treat, in the participants enrolled in the MRI substudy with a valid MRI scan at week 52. The SURPASS-3 clinical trial is registered with ClinicalTrials.gov, NCT03882970, and is complete.
Participants were assessed for eligibility and recruited from April 1, 2019, to Nov 15, 2019. Among 502 participants assessed for eligibility to participate in the MRI substudy, 296 were enrolled, and 246 had a valid week 52 MRI scan and were included in the post-hoc analyses (tirzepatide 5 mg, n=63; tirzepatide 10 mg, n=60; tirzepatide 15 mg, n=67; insulin degludec, n=56; 147 [59·8%] male participants and 99 [40·2%] female participants). At baseline, overall mean age was 56·0 years (SD 9·9), median duration of type 2 diabetes was 6·7 years (IQR 3·7 to 10·7), mean HbA was 8·3% (SD 0·9), mean BMI was 33·4 kg/m (SD 4·8), and 76 (30·9%) were on an SGLT-2 inhibitor. Mean baseline muscle fat infiltration, muscle volume, and muscle volume Z scores were similar between the pooled tirzepatide group and insulin degludec group. For the pooled and individual tirzepatide dose groups, significant reductions were observed from baseline to week 52 in muscle fat infiltration (for pooled tirzepatide, mean change -0·36 percentage points [95% CI -0·48 to -0·25], p<0·0001), muscle volume (-0·64 L [95% CI -0·74 to -0·54], p<0·0001), and muscle volume Z score (-0·22 [95% CI -0·29 to -0·15], p<0·0001), which occurred in the context of significant weight reduction. Insulin degludec was associated with a modest and significant increase in bodyweight and muscle volume, but no significant change in the other variables. The changes in all three muscle composition variables with pooled tirzepatide were significantly different compared to those with insulin degludec. In tirzepatide-treated participants, observed muscle volume changes across all tirzepatide doses were similar to population-based estimated changes (for pooled tirzepatide, mean difference vs population-based estimate, -0·04 L [95% CI -0·11 to 0·03], p=0·22); whereas, observed reductions in muscle fat infiltration across all doses were significantly greater than population-based estimates (for pooled tirzepatide, mean difference -0·42 percentage points [95% CI -0·54 to -0·31], p<0·0001), and the observed reduction in muscle volume Z score with tirzepatide 15 mg was significantly greater than the population-based estimate (mean difference -0·18 [95% CI -0·29 to -0·07], p=0·0016).
In the SURPASS-3 MRI substudy, in the context of significant improvements in bodyweight and fat distribution, tirzepatide treatment was associated with potentially favourable changes in muscle fat infiltration and reductions in muscle volume broadly in accordance with the general association between changes in muscle volume and bodyweight. The present findings provide additional information on the potential effect of tirzepatide on muscle health that might help health-care providers when deciding among treatment options for individual patients.
Eli Lilly and Company.
显著的体重减轻通常与肌肉量减少有关。在2型糖尿病试验中,替尔泊肽与体重显著降低有关,并且在SURPASS-3 MRI子研究中对体脂分布有有益影响。这项事后探索性分析研究了替尔泊肽治疗与大腿肌肉体积、肌肉体积Z评分和肌肉脂肪浸润变化之间的关联,旨在利用来自英国生物银行参与者的纵向MRI数据对结果进行背景分析。
SURPASS-3是一项随机、开放标签、平行组、3期试验。SURPASS-3的多中心(45个地点)和多国(8个国家)MRI子研究纳入了未使用过胰岛素的2型糖尿病成年患者(年龄≥18岁),这些患者正在接受二甲双胍治疗,使用或未使用钠-葡萄糖协同转运蛋白2(SGLT-2)抑制剂,糖化血红蛋白(HbA)为7.0%-10.5%(53-91 mmol/mol),体重指数(BMI)至少为25 kg/m²,脂肪肝指数至少为60。参与者被随机分配(1:1:1:1),接受每周一次皮下注射替尔泊肽(5、10或15 mg),或每天一次皮下注射滴定剂量的德谷胰岛素。在基线和第52周通过MRI对大腿肌肉脂肪浸润、肌肉体积和肌肉体积Z评分(不受性别、身高、体重和BMI影响)进行量化。在这项事后分析中,我们使用配对t检验评估了替尔泊肽组(5 mg、10 mg和15 mg合并组以及各剂量组)和德谷胰岛素组中基线和第52周肌肉成分平均值之间的差异,并通过调整后的协方差分析模型评估了合并替尔泊肽与德谷胰岛素在肌肉成分变化方面的差异。使用配对t检验将观察到的肌肉脂肪浸润、肌肉体积和肌肉体积Z评分的变化与根据拟合到英国生物银行数据(n = 2942)的多元线性回归模型计算的基于人群的估计值进行比较,以捕捉与体重变化的关联。分析采用改良意向性治疗,纳入在第52周进行有效MRI扫描的MRI子研究参与者。SURPASS-3临床试验已在ClinicalTrials.gov注册,注册号为NCT03882970,且已完成。
参与者于2019年4月1日至2019年11月15日进行资格评估并招募。在502名评估参与MRI子研究资格的参与者中,296名被纳入,246名在第52周有有效的MRI扫描并被纳入事后分析(替尔泊肽5 mg,n = 63;替尔泊肽10 mg,n = 60;替尔泊肽15 mg,n = 67;德谷胰岛素,n = 56;147名[59.8%]男性参与者和99名[40.2%]女性参与者)。基线时,总体平均年龄为(56.0±9.9)岁,2型糖尿病中位病程为6.7年(四分位间距3.7至10.7年),平均HbA为8.3%(标准差0.9),平均BMI为33.4 kg/m²(标准差4.8),76名(30.9%)使用SGLT-2抑制剂。合并替尔泊肽组和德谷胰岛素组之间的平均基线肌肉脂肪浸润、肌肉体积和肌肉体积Z评分相似。对于合并和各替尔泊肽剂量组,从基线到第52周观察到肌肉脂肪浸润(合并替尔泊肽,平均变化-0.36个百分点[95%置信区间-0.48至-0.25],p<0.0001)、肌肉体积(-0.64 L[95%置信区间-0.74至-0.54],p<0.0001)和肌肉体积Z评分(-0.22[95%置信区间-0.29至-0.15],p<0.0001)显著降低,这发生在体重显著减轻的背景下。德谷胰岛素与体重和肌肉体积适度且显著增加相关,但其他变量无显著变化。合并替尔泊肽与德谷胰岛素相比,所有三个肌肉成分变量的变化均有显著差异。在接受替尔泊肽治疗的参与者中,观察到的所有替尔泊肽剂量下的肌肉体积变化与基于人群的估计变化相似(合并替尔泊肽,与基于人群估计的平均差异为-0.04 L[95%置信区间-0.11至0.03],p = 0.22);然而,观察到的所有剂量下肌肉脂肪浸润的减少显著大于基于人群的估计值(合并替尔泊肽,平均差异-0.42个百分点[95%置信区间-0.54至-0.31],p<0.0001),并且替尔泊肽15 mg时观察到的肌肉体积Z评分降低显著大于基于人群的估计值(平均差异-0.18[95%置信区间-0.29至-0.07],p = 0.0016)。
在SURPASS-3 MRI子研究中,在体重和脂肪分布显著改善的背景下,替尔泊肽治疗与肌肉脂肪浸润的潜在有利变化以及肌肉体积的减少相关,这大致符合肌肉体积变化与体重之间的一般关联。本研究结果提供了关于替尔泊肽对肌肉健康潜在影响的额外信息,这可能有助于医疗保健提供者在为个体患者选择治疗方案时做出决策。
礼来公司。