Novel pharmacotherapies for weight loss: Understanding the role of incretins to enable weight loss and improved health outcomes DOI
Thomas Först, Christophe De Block, Stefano Del Prato

et al.

Diabetes Obesity and Metabolism, Journal Year: 2025, Volume and Issue: unknown

Published: Feb. 11, 2025

Abstract Obesity and type 2 diabetes mellitus (T2D) are widespread diseases that significantly impact cardiovascular renal morbidity mortality. In the recent years, intensive research has been performed to assess role of adipose tissue body fat distribution in development metabolic non‐metabolic complications individuals with obesity. addition lifestyle modifications, glucagon‐like peptide‐1 receptor agonists (GLP‐1‐RA) have become a meaningful treatment expansion for management both disorders. improving control reducing weight, GLP‐1‐RAs reduces events obesity without diabetes. These important benefits triggered new interest other enteroendocrine enteropancreatic peptides treating its consequences. The first peptide dual‐agonist targeting glucose‐dependent insulinotropic polypeptide (GIP) GLP‐1 receptors approved T2D GIP/GLP‐1 dual‐agonism appear provide better greater weight reduction compared GLP‐1‐R mono‐agonism. Other non‐peptide co‐agonists clinical obesity, T2D, dysfunction‐associated steatotic liver disease (MASLD) This narrative review aims summarize available data on emerging based approaches efficacy measures, side effects, limitations open challenges will also be addressed.

Language: Английский

Glucagon‐like peptide‐1 receptor agonist‐based agents and weight loss composition: Filling the gaps DOI
Robert L. Dubin, Steven B. Heymsfield, Éric Ravussin

et al.

Diabetes Obesity and Metabolism, Journal Year: 2024, Volume and Issue: unknown

Published: Sept. 30, 2024

Abstract Excess adiposity is at the root of type 2 diabetes (T2D). Glucagon‐like peptide‐1 receptor agonists (GLP‐1RAs) have emerged as first‐line treatments for T2D based on significant weight loss results. The composition using most diets consists <25% fat‐free mass (FFM) loss, with remainder from fat stores. Higher amounts (achieved metabolic bariatric surgery) result in greater reductions FFM. Our aim was to assess impact that GLP‐1RA‐based We analysed studies reported changes FFM following agents: exenatide, liraglutide, semaglutide, and dual incretin agonist tirzepatide. performed an analysis various interventions provide a reference expected evaluated dual‐energy X‐ray absorptiometry (DXA) measuring (a crude surrogate skeletal muscle). In evaluating percentage lost (%FFML) equal ΔFFM/total change. %FFML agents between 20% 40%. 28 clinical trials evaluated, proportion highly variable, but majority exceeding 25%. review limited small substudies use DXA, which does not measure muscle directly. Since contains variable amount (approximately 55%), this indirect may explain heterogeneity data. Assessing quantity quality advanced imaging (magnetic resonance imaging) functional testing will help fill gaps our current understanding.

Language: Английский

Citations

5

Novel pharmacotherapies for weight loss: Understanding the role of incretins to enable weight loss and improved health outcomes DOI
Thomas Först, Christophe De Block, Stefano Del Prato

et al.

Diabetes Obesity and Metabolism, Journal Year: 2025, Volume and Issue: unknown

Published: Feb. 11, 2025

Abstract Obesity and type 2 diabetes mellitus (T2D) are widespread diseases that significantly impact cardiovascular renal morbidity mortality. In the recent years, intensive research has been performed to assess role of adipose tissue body fat distribution in development metabolic non‐metabolic complications individuals with obesity. addition lifestyle modifications, glucagon‐like peptide‐1 receptor agonists (GLP‐1‐RA) have become a meaningful treatment expansion for management both disorders. improving control reducing weight, GLP‐1‐RAs reduces events obesity without diabetes. These important benefits triggered new interest other enteroendocrine enteropancreatic peptides treating its consequences. The first peptide dual‐agonist targeting glucose‐dependent insulinotropic polypeptide (GIP) GLP‐1 receptors approved T2D GIP/GLP‐1 dual‐agonism appear provide better greater weight reduction compared GLP‐1‐R mono‐agonism. Other non‐peptide co‐agonists clinical obesity, T2D, dysfunction‐associated steatotic liver disease (MASLD) This narrative review aims summarize available data on emerging based approaches efficacy measures, side effects, limitations open challenges will also be addressed.

Language: Английский

Citations

0