Obesity is a complex multifactorial condition that is associated with increased risk of various diseases and higher all-cause mortality. It contributes to the development of numerous comorbidities and adverse clinical outcomes, and is reciprocally influenced by certain medical conditions, further complicating effective weight management. Key management strategies include diet, physical activity, and behavioral interventions, with pharmacotherapy and bariatric surgery serving as adjuncts to enhance weight loss and improve long-term maintenance. As of 2024, several anti-obesity medications (AOMs) have been approved in Korea, including orlistat, naltrexone/bupropion, phentermine/topiramate, and nutrient-stimulated hormone (NuSH)-based AOMs such as liraglutide, semaglutide, and tirzepatide. The selection of AOMs requires careful consideration of individual comorbidities to optimize therapeutic outcomes, while minimizing adverse effects. For patients without comorbidities, all AOMs are viable options. NuSH-based AOMs are primarily recommended for patients with type 2 diabetes or prediabetes because of their superior efficacy, though other AOMs may also be considered. For individuals at high risk of cardiovascular disease, NuSH-based AOMs with proven effectiveness in reducing major adverse cardiovascular events are preferred. In patients with psychiatric disorders, all AOMs should be used with caution and under close monitoring. AOMs are contraindicated in patients with severe hepatic or renal impairment and in pregnant or breastfeeding women. Personalized, comorbidity-focused pharmacological strategies are essential to achieve significant and sustainable weight loss. This review examines the role of tailored pharmacotherapy in obesity management, and emphasizes the importance of individualized treatment approaches to address the unique health profiles of individuals with obesity and improve therapeutic outcomes.
Anti-obesity medication, Orlistat, Naltrexone/bupropion, Phentermine/topiramate, Nutrient-stimulated hormone, Glucagon-like peptide-1 receptor agonist
2024.12.30 | ASSIGNED_DOI | |
2024.12.31 | PUBLISHED |