[Anti-obesity drugs : from previous disappointments to new hopes].
Rev Med Liege · 2023
Last updated 2026-05-28Most older anti-obesity drugs were withdrawn due to serious side effects like heart and brain risks. Newer drugs, such as GLP-1 receptor agonists like liraglutide and semaglutide, originally used for diabetes, are now prescribed at higher doses for weight loss. A newer drug called tirzepatide, which targets both GLP-1 and GIP receptors, is being tested and appears to be more effective for lowering blood sugar and aiding weight loss.
AI summary of the abstract below.
| Journal | Rev Med Liege, 2023 |
|---|---|
| Citations | 3 |
| Relative citation ratio | 0.47 |
| NIH percentile | 27 |
| Molecules | — |
| Conditions studied | Obesity |
Abstract
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.
Verbatim abstract via PubMed 36924152 ↗