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Tesamorelin

Egrifta, TH9507

Quick Stats
Studies 64
Trials 24
Score 3
2014 pubmed 70 citations

Effect of tesamorelin on visceral fat and liver fat in HIV-infected patients with abdominal fat accumulation: a randomized clinical trial.

Stanley. Takara L TL; Feldpausch. Meghan N MN; Oh. Jinhee J; Branch. Karen L KL; Lee. Hang H; Torriani. Martin M; Grinspoon. Steven K SK

Key Findings

  • Tesamorelin reduced visceral adipose tissue by an average of 34 cm² compared to a slight increase in the placebo group.
  • Liver fat decreased by about 2 % (lipid‑to‑water ratio) in the tesamorelin group, while it rose slightly in the placebo group.
  • Fasting glucose rose modestly after 2 weeks of treatment but was not significantly different from placebo after 6 months.

Practical Outcomes

  • For biohackers interested in cutting visceral and liver fat, tesamorelin (2 mg daily subcutaneously) shows promise over a 6‑month period, but the early glucose spike suggests monitoring blood sugar is essential. The drug is currently approved only for HIV‑related fat redistribution, so off‑label use carries unknown long‑term risks and should be approached cautiously.

Summary

In a 6‑month trial, HIV patients who got daily injections of tesamorelin lost a noticeable amount of belly fat and had a small drop in liver fat, while their blood sugar only rose briefly early on and then returned to normal.

Abstract

Among patients infected with human immunodeficiency virus (HIV), visceral adiposity is associated with metabolic dysregulation and ectopic fat accumulation. Tesamorelin, a growth hormone-releasing hormone analog, specifically targets visceral fat reduction but its effects on liver fat are unknown. To investigate the effect of tesamorelin on visceral and liver fat. Double-blind, randomized, placebo-controlled trial conducted among 50 antiretroviral-treated HIV-infected men and women with abdominal fat accumulation at Massachusetts General Hospital in Boston. The first patient was enrolled on January 10, 2011; for the final patient, the 6-month study visit was completed on September 6, 2013. Participants were randomized to receive tesamorelin, 2 mg (n=28), or placebo (n=22), subcutaneously daily for 6 months. Primary end points were changes in visceral adipose tissue and liver fat. Secondary end points included glucose levels and other metabolic end points. Forty-eight patients received treatment with study drug. Tesamorelin significantly reduced visceral adipose tissue (mean change, -34 cm2 [95% CI, -53 to -15 cm2] with tesamorelin vs 8 cm2 [95% CI, -14 to 30 cm2] with placebo; treatment effect, -42 cm2 [95% CI, -71 to -14 cm2]; P = .005) and liver fat (median change in lipid to water percentage, -2.0% [interquartile range {IQR}, -6.4% to 0.1%] with tesamorelin vs 0.9% [IQR, -0.6% to 3.7%] with placebo; P = .003) over 6 months, for a net treatment effect of -2.9% in lipid to water percentage. Fasting glucose increased in the tesamorelin group at 2 weeks (mean change, 9 mg/dL [95% CI, 5-13 mg/dL] vs 2 mg/dL [95% CI, -3 to 8 mg/dL] in the placebo group; treatment effect, 7 mg/dL [95% CI, 1-14 mg/dL]; P = .03), but changes at 6 months in fasting glucose (mean change, 4 mg/dL [95% CI, -2 to 10 mg/dL] with tesamorelin vs 2 mg/dL [95% CI, -4 to 7 mg/dL] with placebo; treatment effect, 2 mg/dL [95% CI, -6 to 10 mg/dL]; P = .72 overall across time points) and 2-hour glucose (mean change, -1 mg/dL [95% CI, -18 to 15 mg/dL] vs -8 mg/dL [95% CI, -24 to 8 mg/dL], respectively; treatment effect, 7 mg/dL [95% CI, -16 to 29 mg/dL]; P = .53 overall across time points) were not significant. In this preliminary study of HIV-infected patients with abdominal fat accumulation, tesamorelin administered for 6 months was associated with reductions in visceral fat and additionally with modest reductions in liver fat. Further studies are needed to determine the clinical importance and long-term consequences of these findings. clinicaltrials.gov Identifier: NCT01263717.

Study Information

Provider

pubmed

Year

2014

Date

2014-07-23T00:00:00.000Z

DOI

10.1001/jama.2014.8334

Citations

70

References

33