Strategies for minimizing muscle loss during use of incretin-mimetic drugs for treatment of obesity.
Jeffrey I MechanickW Scott ButschSandra M ChristensenOsama HamdyZhaoping LiCarla M PradoSteven B HeymsfieldPublished in: Obesity reviews : an official journal of the International Association for the Study of Obesity (2024)
The rapid and widespread clinical adoption of highly effective incretin-mimetic drugs (IMDs), particularly semaglutide and tirzepatide, for the treatment of obesity has outpaced the updating of clinical practice guidelines. Consequently, many patients may be at risk for adverse effects and uncertain long-term outcomes related to the use of these drugs. Of emerging concern is the loss of skeletal muscle mass and function that can accompany rapid substantial weight reduction; such losses can lead to reduced functional and metabolic health, weight cycling, compromised quality of life, and other adverse outcomes. Available evidence suggests that clinical trial participants receiving IMDs for the treatment of obesity lost 10% or more of their muscle mass during the 68- to 72-week interventions, approximately equivalent to 20 years of age-related muscle loss. The ability to maintain muscle mass during caloric restriction-induced weight reduction is influenced by two key factors: nutrition and physical exercise. Nutrition therapy should ensure adequate intake and absorption of high-quality protein and micronutrients, which may require the use of oral nutritional supplements. Additionally, concurrent physical activity, especially resistance training, has been shown to effectively minimize loss of muscle mass and function during weight reduction therapy. All patients receiving IMDs for obesity should participate in comprehensive treatment programs emphasizing adequate protein and micronutrient intakes, as well as resistance training, to preserve muscle mass and function, maximize the benefit of IMD therapy, and minimize potential risks.
Keyphrases
- physical activity
- weight loss
- resistance training
- weight gain
- metabolic syndrome
- type diabetes
- body mass index
- clinical trial
- insulin resistance
- public health
- healthcare
- end stage renal disease
- high intensity
- skeletal muscle
- chronic kidney disease
- randomized controlled trial
- high fat diet induced
- radiation therapy
- climate change
- adipose tissue
- body weight
- depressive symptoms
- risk assessment
- mental health
- open label
- human health
- squamous cell carcinoma
- social media
- mesenchymal stem cells
- combination therapy
- double blind
- health information
- patient reported outcomes
- phase iii
- phase ii
- protein protein