Menu
Peptide Database
Results
No peptides found
Featured

Use search to browse all 100+ peptides

Tesamorelin

Egrifta, TH9507

Quick Stats
Studies 64
Trials 24
Score 3
2012 pubmed 22 citations

Reduction in visceral adiposity is associated with an improved metabolic profile in HIV-infected patients receiving tesamorelin.

Stanley. Takara L TL; Falutz. Julian J; Marsolais. Christian C; Morin. Josée J; Soulban. Graziella G; Mamputu. Jean-Claude JC; Assaad. Hani H; Turner. Ralph R; Grinspoon. Steven K SK

Key Findings

  • Tesamorelin users who cut visceral fat ≥8% saw a 0.6‑0.8 mmol/L drop in triglycerides versus almost no change in non‑responders.
  • Glucose control was better in responders: smaller rises (or slight drops) in fasting glucose and hemoglobin A1c compared with non‑responders.
  • Adiponectin, a hormone linked to insulin sensitivity, increased significantly only in the responder group.

Practical Outcomes

  • For biohackers aiming to lower visceral fat and improve metabolic health, tesamorelin shows that a meaningful reduction in belly fat can translate into better blood lipids and glucose handling. However, the data come from HIV‑positive patients, so effects in healthy individuals are uncertain. If you can access tesamorelin, targeting at least an 8% VAT loss may be a useful benchmark for metabolic benefits, but monitor blood sugars and lipids closely.

Summary

In people with HIV, the drug tesamorelin shrank belly fat (visceral fat) by at least 8% and, in those who responded, also lowered triglycerides, raised good‑fat hormone adiponectin, and kept blood sugar more stable over a year. The metabolic improvements tracked with how much belly fat was lost.

Abstract

Tesamorelin, a growth hormone-releasing hormone analogue, decreases visceral adipose tissue (VAT) by 15%-20% over 6-12 months in individuals with human immunodeficiency virus (HIV)-associated abdominal adiposity, but it is unknown whether VAT reduction is directly associated with endocrine and metabolic changes. In 2 phase III, randomized, double-blind studies, men and women with HIV-associated abdominal fat accumulation were randomly assigned (ratio, 2:1) to receive tesamorelin or placebo for 26 weeks. At week 26, patients initially receiving tesamorelin were randomly assigned to continue receiving tesamorelin or to receive placebo for an additional 26 weeks. In per-protocol analysis of 402 subjects initially randomly assigned to receive tesamorelin, those with ≥8% reduction in VAT were defined a priori as responders per the statistical analysis plan. Post hoc analyses were performed to assess differences between responders and nonresponders. Compared with tesamorelin nonresponders, responders experienced greater mean (±SD) reduction in triglyceride levels (26 weeks: -0.6 ± 1.7 mmol/L vs -0.1 ± 1.2 mmol/L [P = .005]; 52 weeks: -0.8 ± 1.8 mmol/L vs 0.0 ± 1.1 mmol/L [P = .003]) and attenuated changes in fasting glucose levels (26 weeks: 1 ± 16 mg/dL vs 5 ± 14 mg/dL [P = .01]; 52 weeks: -1 ± 14 mg/dL vs 8 ± 17 mg/dL [P < .001]), hemoglobin A1c levels (26 weeks: 0.1 ± 0.3% vs 0.3 ± 0.4% [P < .001]; 52 weeks: 0.0 ± 0.3% vs 0.2 ± 0.5% [P = .003]), and other parameters of glucose homeostasis. Similar patterns were seen for adiponectin levels, with significant improvement in responders vs nonresponders. Changes in lipid levels and glucose homeostasis were significantly associated with percentage change in VAT. In contrast to nonresponders, HIV-infected patients receiving tesamorelin with ≥8% reduction in VAT have significantly improved triglyceride levels, adiponectin levels, and preservation of glucose homeostasis over 52 weeks of treatment. CLINICALTRIALS.GOV REGISTRATION: NCT00123253, NCT00435136, NCT00608023.

Study Information

Provider

pubmed

Year

2012

Date

2012-04-10T00:00:00.000Z

DOI

10.1093/cid/cis251

Citations

22

References

34