Related Experiment Video
Updated: Jun 6, 2025

Study of In Vivo Glucose Metabolism in High-fat Diet-fed Mice Using Oral Glucose Tolerance Test OGTT and Insulin Tolerance Test ITT
Published on: January 7, 2018
Sodium-Glucose Cotransporter 2 Inhibitors Improve Body Composition by Increasing the Skeletal Muscle Mass/Fat Mass
Sara Volpe1, Alfredo Vozza1, Giuseppe Lisco1
1Interdisciplinary Department of Medicine, School of Medicine, University of Bari "Aldo Moro", Piazza Giulio Cesare 11, 70124 Bari, Italy.
Background:
Sodium-glucose cotransporter 2 inhibitors (SGLT2is) induce body weight loss, but their effect on skeletal muscle mass (SMM) and strength needs to be better elucidated.
Objectives:
This study aimed to evaluate the effects of SGLT2i on SMM in a real-life population setting of patients with type 2 diabetes (T2D). Secondary outcomes included changes in liver steatosis and in anthropometric and glucometabolic parameters.
Methods:
Seventy-one patients were treated with SGLT2is as an add-on to metformin for 52 consecutive weeks. Visits were scheduled at baseline (T0) and after 6 (T6) and 12 months of therapy (T12) and included the checking of laboratory tests, measurement of anthropometric parameters, bioimpedance analysis of body composition, and abdominal ultrasound (US).
Results:
Fat mass (FM) and visceral adipose tissue (VAT) progressively decreased compared to the baseline (FM: -2.9 ± 0.6 kg at T6; -2.8 ± 0.6 kg at T12; VAT: -0.3 ± 0.1 L at T6; -0.4 ± 0.1 L at T12; all p < 0.01). Changes in SMM were less pronounced (-0.4 ± 0.3 kg at T6, ns; -0.7 ± 0.4 kg at T12, p < 0.05), yielding a beneficial increase in the SMM/FM ratio (+0.3 ± 0.05 at T6 and +0.2 ± 0.05 at T12, all p < 0.01). No significant changes in sarcopenia, sarcopenic obesity, fat-free mass, muscle strength, and water compartments were observed at the end of the follow-up period. Anthropometric and glucometabolic parameters, insulin resistance, liver enzymes, and biometric indices and US grading of hepatic steatosis improved throughout this study.
Conclusions:
In a real-life setting, SGLT2i therapy is associated with weight loss attributable to FM rather than SMM loss without any relevant deterioration in muscle strength. In addition, SGLT2is proved to have beneficial effects on steatotic liver disease.
Insights
Sodium-glucose cotransporter 2 inhibitors (SGLT2is) aid weight loss in type 2 diabetes patients by reducing fat mass, not skeletal muscle mass. This therapy also improves liver steatosis without negatively impacting muscle strength.
Area of Science:
- Endocrinology
- Metabolic Diseases
- Pharmacology
Background:
- Sodium-glucose cotransporter 2 inhibitors (SGLT2is) are known to induce weight loss.
- The impact of SGLT2is on skeletal muscle mass (SMM) and strength requires further investigation, particularly in real-world clinical settings.
Purpose of the Study:
- To evaluate the effects of SGLT2 inhibitors on skeletal muscle mass in patients with type 2 diabetes.
- To assess secondary outcomes including changes in liver steatosis, anthropometric, and glucometabolic parameters.
Main Methods:
- A real-world study involving 71 patients with type 2 diabetes treated with SGLT2 inhibitors as add-on therapy to metformin for 52 weeks.
- Data collection included anthropometric measurements, bioimpedance analysis for body composition, and abdominal ultrasound for liver steatosis assessment at baseline, 6 months, and 12 months.
Main Results:
- SGLT2 inhibitor therapy led to significant reductions in fat mass and visceral adipose tissue.
- While skeletal muscle mass showed a slight decrease, the ratio of SMM to fat mass improved significantly.
- Improvements were observed in anthropometric and glucometabolic parameters, insulin resistance, and hepatic steatosis.
Conclusions:
- In a real-world setting, SGLT2 inhibitors promote weight loss primarily through fat mass reduction, without significant loss of skeletal muscle mass or strength.
- SGLT2 inhibitors demonstrate beneficial effects on non-alcoholic fatty liver disease in patients with type 2 diabetes.
More Related Videos
12:59Improving Strength, Power, Muscle Aerobic Capacity, and Glucose Tolerance through Short-term Progressive Strength Training Among Elderly People
Published on: July 5, 2017
08:03Glucose Uptake Measurement and Response to Insulin Stimulation in In Vitro Cultured Human Primary Myotubes
Published on: June 25, 2017
Related Concept Videos
Oral Hypoglycemic Agents: Biguanides and Glitazones
Diabetes Mellitus: Type 2 and Gestational
Glucose Transporters
Facilitated diffusion-glucose transporters (GLUTs) are encoded by the solute-linked carrier (SLC) family 2, subfamily A gene family, or SLC2A. The 14 GLUT protein members are distributed into three classes:
Oral Hypoglycemic Agents: α-Glucosidase Inhibitors
Acarbose and miglitol are...
Carbohydrate Metabolism
Starch accounts for approximately 60% of the carbohydrates consumed by humans. Since amylase enzymes cannot function in the stomach's acidic environment, starch can only be digested in the mouth and small intestine. Simple sugars are found naturally in milk and fruits in...
Oral Hypoglycemic Agents: Glinides