Galindo Rodolfo J, Lee Clare J, Allen Sheryl Elaine, Dib Anne, Boye Kristina S, Thieu Vivian Thuyanh, Dong Wenxiu, Sapin Hélène, Wiese Russell J
University of Miami Miller School of Medicine, Miami, Florida, USA.
Eli Lilly and Company, Indianapolis, Indiana, USA.
Diabetes Obes Metab. 2025 Oct;27(10):5694-5705. doi: 10.1111/dom.16620. Epub 2025 Jul 24.
To estimate body mass index (BMI) category changes after treatment with tirzepatide as well as potential associations between shifting BMI category and selected cardiometabolic measures and weight-related patient-reported outcomes (PROs) in type 2 diabetes.
This post-hoc analysis analysed data from the SURPASS-1 to -5 trials for weekly tirzepatide (pooled doses) in adults with type 2 diabetes. Changes in BMI category from baseline to Week 40 or 52 (primary endpoint) were assessed and grouped into 'improved' (shift to ≥1 lower category) and 'not improved' (which included 'not improved: stable' [no change in category] or 'not improved: worsened' [shift to ≥1 higher category]). BMI categories were <25 kg/m, 25 to <30 kg/m, 30 to <35 kg/m, 35 to <40 kg/m, and ≥40 kg/m. Associations of changes in selected cardiometabolic parameters and weight-related PROs by BMI shift category were also determined.
Overall, 58.9% of 3559 participants treated with tirzepatide shifted to an 'improved' BMI category, and 41.1% were in the 'not improved' BMI category. Participants with an 'improved' versus 'not improved' BMI category had numerically larger mean improvements from baseline in the majority of the selected cardiometabolic parameters at endpoint in all five SURPASS trials. Improvements in weight-related PROs were numerically largest for participants whose BMI category 'improved'.
After tirzepatide treatment, approximately 60% of adults with type 2 diabetes shifted to a lower 'improved' BMI category. This shift was generally associated with numerical improvements in selected cardiometabolic measures and weight-related PROs that may reduce cardiometabolic risk.
评估替尔泊肽治疗后体重指数(BMI)类别变化,以及2型糖尿病患者BMI类别变化与选定的心脏代谢指标和体重相关患者报告结局(PROs)之间的潜在关联。
本事后分析分析了SURPASS-1至-5试验中2型糖尿病成年患者使用每周一次替尔泊肽(汇总剂量)的数据。评估从基线到第40周或第52周BMI类别的变化(主要终点),并分为“改善”(转变为低至少1个类别)和“未改善”(包括“未改善:稳定”[类别无变化]或“未改善:恶化”[转变为高至少1个类别])。BMI类别分别为<25kg/m²、25至<30kg/m²、30至<35kg/m²、35至<40kg/m²和≥40kg/m²。还确定了选定的心脏代谢参数变化和体重相关PROs按BMI转变类别之间的关联。
总体而言,3559名接受替尔泊肽治疗的参与者中,58.9%转变为“改善”的BMI类别,41.1%属于“未改善”的BMI类别。在所有五项SURPASS试验中,“改善”与“未改善”BMI类别的参与者在终点时,大多数选定的心脏代谢参数从基线的平均改善数值更大。BMI类别“改善”的参与者体重相关PROs的改善数值最大。
替尔泊肽治疗后,约60%的2型糖尿病成年患者转变为较低的“改善”BMI类别。这种转变通常与选定的心脏代谢指标和体重相关PROs的数值改善相关,这可能会降低心脏代谢风险。