New insights into the treatment of obesity

被引:69
|
作者
Blueher, Matthias [1 ,2 ,3 ,4 ]
Aras, Mohini [5 ]
Aronne, Louis J. [5 ]
Batterham, Rachel L. [6 ,7 ]
Giorgino, Francesco [8 ]
Ji, Linong [9 ]
Pietilainen, Kirsi H. [10 ,11 ,12 ]
Schnell, Oliver [13 ,14 ]
Tonchevska, Elena [14 ]
Wilding, John P. H. [15 ]
机构
[1] Univ Leipzig, Med Dept Endocrinol 3, Med Ctr, Nephrol,Rheumatol, Leipzig, Germany
[2] Helmholtz Zentrum Munchen, Helmholtz Inst Metab Obes & Vasc Res HI MAG, Leipzig, Germany
[3] Univ Leipzig, Leipzig, Germany
[4] Univ Hosp Leipzig, Leipzig, Germany
[5] Weill Cornell Med, Comprehens Weight Control Ctr, Div Endocrinol Diabet & Metab, New York, NY USA
[6] UCL, Ctr Obes Res, Div Med, London, England
[7] UCLH Biomed Res Ctr, Natl Inst Hlth & Care Res, London, England
[8] Univ Bari Aldo Moro, Dept Precis & Regenerat Med & Ionian Area, Sect Internal Med Endocrinol Androl & Metab Dis, Bari, Italy
[9] Peking Univ, Dept Endocrinol & Metab, Peoples Hosp, Beijing, Peoples R China
[10] Univ Helsinki, Fac Med, Res Program Clin & Mol Metab, Obes Res Unit, Helsinki, Finland
[11] Helsinki Univ Cent Hosp, Abdominal Ctr, HealthyWeightHub, Endocrinol, Helsinki, Finland
[12] Univ Helsinki, Helsinki, Finland
[13] Forschergrp Diabet eV, Munich, Germany
[14] Sciarc GmbH, Baierbrunn, Germany
[15] Univ Liverpool, Inst Life Course & Med Sci, Dept Cardiovasc & Metab Med, Liverpool, Merseyside, England
来源
DIABETES OBESITY & METABOLISM | 2023年 / 25卷 / 08期
关键词
antiobesity drug; drug development; GIP; GLP-1; analogue; incretin therapy; obesity therapy; GLP-1 RECEPTOR AGONIST; CONTROLLED-RELEASE PHENTERMINE/TOPIRAMATE; TYPE-2; DIABETES-MELLITUS; SEMAGLUTIDE; 2.4; MG; 10-YEAR FOLLOW-UP; WEIGHT-LOSS; BARIATRIC SURGERY; DOUBLE-BLIND; METABOLIC SYNDROME; ABDOMINAL OBESITY;
D O I
10.1111/dom.15077
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Obesity is a chronic, progressive and relapsing disease with a rising global prevalence associated with increased morbidity and mortality and reduced quality of life. Treatment of obesity requires a comprehensive medical approach that includes behavioural interventions, pharmacotherapy and bariatric surgery. The degree of weight loss with all approaches is highly heterogeneous, and long-term weight maintenance remains challenging. For years, antiobesity medications have been limited in number, often delivering meagre efficacy and raising numerous safety concerns. Therefore, there is a need for the development of highly efficacious and safe new agents. Recent insights into the complex pathophysiology of obesity have increased our understanding of intervenable targets for pharmacotherapies to treat obesity and improve weight-related cardiometabolic complications, namely, type 2 diabetes, hyperlipidaemia and hypertension. As a result, novel potent therapies have emerged, such as semaglutide, a glucagon-like peptide-1 receptor agonist (GLP-1RA) recently approved for the treatment of obesity. Semaglutide 2.4 mg once weekly significantly reduces body weight by approximately 15%, with simultaneous improvement in cardiometabolic risk factors and physical functioning in people with obesity. Tirzepatide, the first dual glucose-dependent insulinotropic polypeptide (GIP)/GLP-1RA, has recently demonstrated that body weight reduction exceeding 20% in people with obesity and coupled with improved cardiometabolic measures is feasible. Thus, these novel agents promise to narrow the gap between the weight-loss effects of behaviour interventions, previous pharmacotherapies, and bariatric surgery. In this narrative review, we highlight established and emerging therapeutic treatments for long-term obesity management and position them in a framework according to their weight loss effects.
引用
收藏
页码:2058 / 2072
页数:15
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