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Endocrinol Metab (Seoul). 2024;39(2):206-221.

Glucagon-Like Peptide-1 Based Therapies: A New Horizon in Obesity Management.

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제1저자 손장원 · 교신저자 임수

PMID 38626909 PMC11066441 DOI 10.3803/EnM.2024.1940 IF 5.1 내분비대사내과
소속 (2)
  1. Department of Internal Medicine, Bucheon St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Bucheon, Korea.
  2. Department of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Korea.

Abstract

Obesity is a significant risk factor for health issues like type 2 diabetes and cardiovascular disease. It often proves resistant to traditional lifestyle interventions, prompting a need for more precise therapeutic strategies. This has led to a focus on signaling pathways and neuroendocrine mechanisms to develop targeted obesity treatments. Recent developments in obesity management have been revolutionized by introducing novel glucagon-like peptide-1 (GLP-1) based drugs, such as semaglutide and tirzepatide. These drugs are part of an emerging class of nutrient-stimulated hormone-based therapeutics, acting as incretin mimetics to target G-protein-coupled receptors like GLP-1, glucose-dependent insulinotropic polypeptide (GIP), and glucagon. These receptors are vital in regulating body fat and energy balance. The development of multiagonists, including GLP-1-glucagon and GIP-GLP-1-glucagon receptor agonists, especially with the potential for glucagon receptor activation, marks a significant advancement in the field. This review covers the development and clinical efficacy of various GLP-1-based therapeutics, exploring the challenges and future directions in obesity management.

Keywords

GlucagonGlucagon-like peptide-1 receptor agonistsGlucose-dependent insulinotropic polypeptideMultiagonistObesity

Figures

Fig. 1.
Fig. 1. Effects of glucagon-like peptide-1 (GLP-1), glucose-dependent insulinotropic polypeptide (GIP), and glucagon on various vital organs and tissues. Modified from Lim et al. [37], with permission from Elsevier. ANP, atrial natriuretic peptide; BMD, bone mineral density.
Fig. 2.
Fig. 2. Structures of formulations of glucagon-like peptide-1 receptor agonists (GLP-1RAs) and glucose-dependent insulinotropic polypeptide/ GLP-1RA. Modified from Tschop et al. [36]. GIP, glucose-dependent insulinotropic polypeptide.
Fig. 3.
Fig. 3. Comparison of bodyweight (A) and abdominal visceral fat (B) from baseline to week 68 for semaglutide 2.4 mg, semaglutide 1.7 mg, and placebo in Janpanese and Korean people with obesity. Adapted from Kadowaki et al. [49], with permission from Elsevier. VFA, visceral fat area.

그림 출처: PubMed Central 공개 논문 (PMC11066441)

Conflict of interest statement

CONFLICTS OF INTEREST . No potential conflict of interest relevant to this article was reported.

그 밖의 정보
출판 형태
Journal Article, Review, Research Support, Non-U.S. Gov't
저널
Endocrinology and metabolism (Seoul, Korea) · eISSN 2093-5978
전자 출판
2024-04-16
MeSH
Humans · Obesity* / drug therapy · Glucagon-Like Peptide 1* / therapeutic use / metabolism · Glucagon-Like Peptides / therapeutic use · Obesity Management / methods · Animals · Anti-Obesity Agents / therapeutic use · Glucagon-Like Peptide-1 Receptor Agonists · Semaglutide
Substances
Glucagon-Like Peptide 1 · Glucagon-Like Peptides · Anti-Obesity Agents · Glucagon-Like Peptide-1 Receptor Agonists · Semaglutide
참고문헌
114편