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Weight Loss That Lasts: Reviewing the Long-Term Impact of GLP-1 Receptor Agonists.

Systematic ReviewModerate evidence

This record provides bibliographic details and links to the original research. An editorial study breakdown is not available.

What the researchers found

GLP-1 receptor agonists (semaglutide, liraglutide, tirzepatide, exenatide) show sustained weight loss and acceptable safety profiles across trials lasting 40-120 weeks. GI side effects are the most common adverse events. Obesity should be treated as a chronic condition requiring long-term medication.

Why it matters

Compiles the long-term evidence supporting GLP-1RAs for obesity, reinforcing that these drugs maintain efficacy over years and that obesity management is a long-term commitment.

The numbers in context

Studies from 2018-2025. Treatment durations 40-120 weeks. Agents: semaglutide, liraglutide, tirzepatide, exenatide. Populations: adults with/without T2D, adolescents with severe obesity. Sustained weight loss. GI side effects most common.

How the study worked

Systematic review of high-quality RCTs evaluating long-term efficacy and safety of GLP-1RAs for obesity (2018-2025). Assessed weight loss, glycemic control, and adverse events.

Who was studied

Adults with and without T2D, and adolescents with severe obesity

What this study cannot tell us

Limited follow-up beyond 2 years. Population diversity in available trials is limited. Real-world generalizability uncertain. Weight regain after cessation not fully characterized across all agents.

Read the original research

Weight Loss That Lasts: Reviewing the Long-Term Impact of GLP-1 Receptor Agonists.

Cureus, 17(7), e88334

Citation

Shah, Md Yasir; Mohammad, Ahmad; Bashir Ahmed Samejo, Rabia; Rana, Siddharth; Singla, Shivam; Aurangzeb, Raja Irsalan; Tariq, Muhammad M; Zamir, Muhammad Hamza; Farooq, Umer; Aurangzeb, Raja Faizan; Singla, Bhavna; Rehman, Abdur. (2025). Weight Loss That Lasts: Reviewing the Long-Term Impact of GLP-1 Receptor Agonists.. Cureus, 17(7), e88334. https://doi.org/10.7759/cureus.88334