Liraglutide Reduces Liver Steatosis and Improves Metabolic Indices in Obese Patients Without Diabetes: A 3-Month Prospective Study.
Int J Mol Sci · 2025
Last updated 2026-05-28In a 3-month study of 28 obese adults without diabetes, daily liraglutide injections reduced liver fat as measured by FibroScan (from 305 to 268 dB/m) and improved some liver and insulin resistance markers. Weight loss occurred, but traditional insulin resistance measures did not change, while two other insulin resistance scores did improve.
AI summary of the abstract below.
| Journal | Int J Mol Sci, 2025 |
|---|---|
| Citations | 5 |
| Relative citation ratio | 1.92 |
| Molecules | liraglutide |
| Conditions studied | Obesity, Mash |
Abstract
Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) is a leading cause of liver cirrhosis, with its global prevalence rising due to obesity, insulin resistance, and type 2 diabetes mellitus. While bariatric surgery remains effective for weight loss, Glucagon-Like Peptide-1 analogs such as liraglutide are emerging as promising pharmacological treatments. This study aimed to evaluate the effects of a 3-month liraglutide treatment on liver steatosis, subclinical markers, and insulin resistance in non-diabetic, obese patients with MASLD. Twenty-eight obese adults (BMI ≥ 30 kg/m) were treated with daily subcutaneous liraglutide injections for three months. Liver steatosis was assessed using FibroScan (CAP score) and non-invasive indices (Hepatic Steatosis Index-HSI, and NAFLD Liver Fat Score-NLFS). Insulin resistance was measured with conventional markers (HOMA-IR, QUICKI) and triglyceride-based indices (METS-IR, TyG). Liraglutide significantly reduced liver steatosis (CAP score: 305 to 268 dB/m, < 0.05) and improved HSI, while NLFS remained unchanged. Despite significant weight loss, traditional insulin resistance markers remained unchanged, while METS-IR and TyG improved. Liraglutide therapy improved liver steatosis and triglyceride-based insulin resistance markers in non-diabetic obese patients with MASLD. These findings support the use of liraglutide, highlighting the value of personalized approaches and alternative insulin resistance assessments in MASLD management.
Verbatim abstract via PubMed 40565353 ↗
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