New anti-obesity drugs mimicking intestinal hormones like GLP-1 and GIP show promise in reducing body fat and improving cardio-metabolic health.
The Director General of Health Services has imposed prescribing restrictions due to potential misuse and adverse effects.
Semaglutide, a GLP-1 agonist, was added to the WHO's list of essential medicines in 2025 for treating obesity and diabetes.
Cardiovascular diseases and diabetes cause 23-25 million deaths annually worldwide, with a third of all deaths in India.
Detailed Insights:
India's generic drug industry significantly impacted access to affordable medicines, especially during the HIV-AIDS pandemic, after adopting "process patenting" in 1970.
As semaglutide patents expire, Indian manufacturers aim to produce affordable generic versions, potentially costing 25-30% of the current price.
The Doha Declaration (2001) allows countries to relax patent rules for public health threats, relevant to cardiovascular diseases and diabetes.
GLP-1 agonists can help manage high body fat, diabetes, hypertension, and abnormal blood lipids, particularly addressing inflammation in abdominal fat common among Indians.
Potential adverse effects of these drugs include gastrointestinal issues, mental health disturbances, visual problems, bone thinning, and sarcopenia (muscle loss), a concern for Indians with low lean muscle mass.
Discontinuing these drugs may lead to rebound weight gain and loss of cardio-metabolic benefits, necessitating prolonged therapy with associated costs and side effects.
Scientific/Technical Concepts Involved:
GLP-1 (Glucagon-like Peptide): An intestinal hormone that stimulates insulin release and reduces glucagon secretion, lowering blood sugar levels.
GIP (Gastric Inhibitory Peptide): An intestinal hormone that stimulates insulin secretion in response to glucose.
Sarcopenia: The loss of skeletal muscle mass and strength, often associated with aging or certain medical conditions.