Tesamorelin: a growth hormone-releasing factor analogue for HIV-associated lipodystrophy.
Spooner. Linda M LM; Olin. Jacqueline L JL
Key Findings
- Significant reduction in waist circumference and visceral adipose tissue after 26 weeks
- Improvements in body‑image scores alongside the fat loss
- Effects were maintained during 26‑week extensions with no negative impact on glucose or lipid levels
Practical Outcomes
- For biohackers interested in cutting visceral fat, tesamorelin shows it can work quickly and safely in HIV patients, but it’s not yet proven or approved for general use. The high cost and limited long‑term data mean it’s a cautious, off‑label experiment rather than a go‑to protocol for most people.
Summary
Tesamorelin, a drug that mimics a natural hormone, was shown in two big studies to shrink belly fat and the dangerous fat around organs in people with HIV who have a condition called lipodystrophy. The shrinkage lasted up to a year and people felt better about their bodies, without hurting blood sugar or cholesterol. However, it’s pricey, only approved for HIV‑related fat issues, and we don’t yet know the very long‑term safety or how well it works for folks without HIV.
Abstract
To evaluate the efficacy and safety of tesamorelin, a growth hormone releasing factor analogue approved by the Food and Drug Administration in November 2010 for the treatment of lipodystrophy associated with HIV infection. Literature was obtained through MEDLINE (1948-November 2011) and International Pharmaceutical Abstracts (1970-October 2011) using the search terms tesamorelin, TH9507, growth hormone releasing factor, and HIV-associated lipodystrophy syndrome. Additional publications were obtained through review of references within primary literature publications as well as pertinent Web sites. All articles published in English identified from the data sources were evaluated and all pertinent information was included. All studies relevant to the evaluation of efficacy and safety of tesamorelin in the management of HIV-associated lipodystrophy were included, with a focus on trials completed in humans. In 2 Phase 3 clinical trials and their pooled analyses, tesamorelin was proven to significantly decrease waist circumference and visceral adipose tissue (VAT) following 26 weeks of treatment. Both trials also demonstrated significant improvements in some subjective body image parameters. Both studies had 26-week extension phases that confirmed maintenance of VAT improvements on treatment without adverse impact on blood glucose and lipid parameters. Limited data support off-label uses of tesamorelin at this time. Tesamorelin is effective in improving visceral adiposity and body image in patients with HIV-associated lipodystrophy over 26-52 weeks of treatment. Potential limitations for its use include high cost and lack of long-term safety and adherence data. Tesamorelin provides a useful treatment option for management of patients with significant lipodystrophy related to HIV infection.
Study Information
pubmed
2012
2012-01-31T00:00:00.000Z
10.1345/aph.1q629