Keywords :
Anti-Obesity Agents; Glucagon-Like Peptide 1; IY9XDZ35W2 (Glucose); Glucagon-Like Peptide-1 Receptor; Hypoglycemic Agents; Humans; Anti-Obesity Agents/pharmacology/therapeutic use; Diabetes Mellitus, Type 2/drug therapy; Glucagon-Like Peptide 1/pharmacology/therapeutic use; Obesity/drug therapy; Glucose/therapeutic use; Glucagon-Like Peptide-1 Receptor/agonists; Hypoglycemic Agents/therapeutic use; Anorectic drugs; Gastrointestinal peptides; Glucagon-like peptide-1; Obesity; Pharmacotherapy; Safety
Abstract :
[en] Both physicians and patients dream of an efficacious and safe pharmacological approach to treat obesity. Unfortunately, most anti-obesity drugs prescribed since the fifties were associated with an unfavourable risk profile that led to numerous withdrawals. Medications issued from pharmaco-chemistry that mainly target brain amines to reduce appetite have been abandoned because of potential cardiovascular and neuropsychiatric toxicities. More recently, biological medications emerged, especially GLP-1 (Glucagon-Like Peptide-1) receptor agonists, well-known to manage type 2 diabetes and now recommended at higher doses for the treatment of obesity (liraglutide, semaglutide). A dual agonist that targets both GLP-1 and GIP (Glucose-dependent Insulinotropic Polypeptide) receptors (tirzepatide) appears to be even more potent as glucose-lowering agent and is currently tested as an anti-obesity agent. Many other pharmacological approaches are currently investigated but they should not mask the importance of life-style measurements.
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