Predictive factors of body weight loss in patients with type 2 diabetes treated with GLP-1 receptor agonists: a 52-week prospective real-life study.
Front Endocrinol (Lausanne) · 2025
Last updated 2026-05-28In a 52-week study of 194 adults with type 2 diabetes starting GLP-1 drugs like semaglutide or dulaglutide, 58% lost at least 5% of their body weight at 6 months, and 49% did so by 12 months. Those who responded better tended to have higher body weight, more fat around the liver, and other specific health factors at the start. Women, younger patients, those with shorter diabetes duration, and those not already taking metformin were more likely to lose weight. Responding early at 6 months was a strong sign of success at 12 months.
AI summary of the abstract below.
| Journal | Front Endocrinol (Lausanne), 2025 |
|---|---|
| Citations | 5 |
| Relative citation ratio | 1.82 |
| Molecules | — |
| Conditions studied | Type 2 Diabetes, Obesity |
Abstract
INTRODUCTION: Glucagon-like peptide-1 receptor agonists (GLP-1RAs) are widely prescribed for their efficacy in glycemic control and weight reduction, but patient response is heterogeneous and predictors of weight loss remain insufficiently defined. This 52-week prospective, observational study aimed to identify predictors of weight reduction (≥5% from baseline) in patients with type 2 diabetes mellitus (T2D) undergoing GLP-1RA therapy (semaglutide or dulaglutide, including oral formulations).
METHODS: A total of 194 adults with T2D initiating GLP-1RA therapy were evaluated at baseline, and after 6, and 12 months of therapy. To identify predictors of weight loss, variables differing between Responders (weight loss ≥5% than baseline) and Non-Responders were evaluated by ROC analysis and tested in univariate and multivariate logistic regression models adjusted for age, gender, GLP-1RA type and dosage.
RESULTS: At 6 and 12 months, 58% and 49% of patients, respectively, achieved the primary outcome. Responders at 12 months exhibited elevated BMI, waist circumference, hepatic steatosis indices, fat mass, and insulin levels at baseline, along with reduced muscle-to-fat and muscle-to-visceral adipose tissue ratios. Moreover, female gender, younger age, shorter disease duration, and non-use of metformin prior to enrollment were significantly associated with response. Notably, early response at 6 months strongly predicted 12-month success.
CONCLUSIONS: Our results highlight a valuable interplay between body composition, liver involvement, and the incretin response, also suggesting a maximal synergistic effect between metformin and GLP-1RAs when treatments are initiated concurrently rather than sequentially. These data provide valuable insights for the development of individualized treatment strategies.
Verbatim abstract via PubMed 41079186 ↗