Long-Term Efficacy and Safety of Anti-Obesity Treatment: Where Do We Stand?
Young Jin TakSang Yeoup LeePublished in: Current obesity reports (2021)
Recent meta-analyses of new anti-obesity drugs and their weight-loss efficacy have shown that the overall placebo-subtracted weight reduction (%) for at least 12 months ranged from 2.9 to 6.8% for the following drugs: phentermine/topiramate (6.8%), liraglutide (5.4%), naltrexone/bupropion (4.0%), orlistat (2.9%), and lorcaserin (3.1%). However, very recently, on February 13, 2020, the US Food and Drug Administration (FDA) ordered the withdrawal of lorcaserin from markets, as a clinical trial to assess drug safety showed an increased risk of cancer. Currently, the anti-obesity medications that have been approved by the FDA for chronic weight management are orlistat, phentermine/topiramate, naltrexone/bupropion, and liraglutide. However, they are costly and may have adverse effects in some individuals. Therefore, drug therapy should be initiated in obese individuals after weighing its benefits and risks. One of the strategies for long-term obesity control is that anti-obesity medications should be tailored for specific patients depending on their chronic conditions, comorbidities, and preferences.
Keyphrases
- weight loss
- bariatric surgery
- weight gain
- metabolic syndrome
- roux en y gastric bypass
- insulin resistance
- gastric bypass
- type diabetes
- clinical trial
- high fat diet induced
- drug administration
- glycemic control
- systematic review
- drug induced
- randomized controlled trial
- body mass index
- end stage renal disease
- meta analyses
- skeletal muscle
- physical activity
- prognostic factors
- stem cells
- open label
- adverse drug
- study protocol
- mesenchymal stem cells
- phase iii
- peritoneal dialysis
- climate change
- papillary thyroid
- decision making