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Tesamorelin

Egrifta, TH9507

Quick Stats
Studies 64
Trials 24
Score 3
2011 pubmed 1 citations

Tesamorelin: a novel therapeutic option for HIV/HAART-associated increased visceral adipose tissue.

Falutz. Julian J

Key Findings

  • Tesamorelin significantly reduces visceral (abdominal) fat in treated HIV patients
  • It improves abnormal lipid profiles while generally preserving glucose homeostasis
  • Visceral fat and metabolic benefits quickly return after stopping the drug, and long‑term cardiovascular impact is unclear

Practical Outcomes

  • For biohackers interested in cutting visceral fat, tesamorelin shows promise but is currently approved only for HIV‑related lipodystrophy. It may be used off‑label with careful blood‑sugar and lipid monitoring, but users need a plan for maintaining results after discontinuation, and should be aware that long‑term safety data are limited.

Summary

Tesamorelin is a lab-made hormone that helps the body release growth hormone naturally. In people with HIV on treatment, it cuts belly fat, improves bad cholesterol numbers, and usually doesn’t mess up blood sugar. The fat comes back quickly if you stop the drug, and we still don’t know the long‑term heart benefits or how to keep the results after stopping.

Abstract

Metabolic complications are common in treated HIV patients. Their etiology is multifactorial and the development of increased abdominal fat contributes to cardiovascular risk and impaired quality of life. Treated patients with fat mass distribution changes have relative growth hormone deficiency. Both pharmacologic and physiologic doses of growth hormone reduce the increased visceral adipose tissue and improve the associated abnormal lipid profiles in short-term studies. However, impaired glucose homeostasis changes and significant musculoskeletal toxicity occurs. A novel growth hormone-releasing factor analogue, tesamorelin, provides a physiologic means of restoring a normal growth hormone secretion profile and reduces increased visceral adipose tissue, improving both abnormal lipid profiles and patients' quality of life. Glucose homeostasis is generally well maintained. Cessation of treatment with either growth hormone or tesamorelin results in a prompt return of truncal obesity. Management strategies for the long-term maintenance of the reduced visceral adipose tissue have not yet been clarified and long-term effects on decreasing cardiovascular risks and improving clinical outcomes are uncertain.

Study Information

Provider

pubmed

Year

2011

Date

2011-06-01T00:00:00.000Z

DOI

10.1358/dot.2011.47.6.1603439

Citations

1