Metabolic effects of a growth hormone-releasing factor in patients with HIV.
Falutz. Julian J; Allas. Soraya S; Blot. Koenraad K; Potvin. Diane D; Kotler. Donald D; Somero. Michael M; Berger. Daniel D; Brown. Stephen S; Richmond. Gary G; Fessel. Jeffrey J; Turner. Ralph R; Grinspoon. Steven S
Key Findings
- Visceral fat decreased 15.2% with tesamorelin versus a 5% increase with placebo
- Triglycerides fell ~50 mg/dL and the total‑cholesterol/HDL ratio improved in the tesamorelin group
- IGF‑I levels rose 81% indicating strong GH axis activation, while glycemic measures stayed unchanged
Practical Outcomes
- Tesamorelin shows promise as a potent agent for reducing visceral fat and improving lipid profiles, but it’s a prescription peptide studied only in HIV patients. Biohackers could consider it for deep‑fat loss, using 2 mg daily subcutaneous injections, but must monitor IGF‑I, lipids, and potential side effects, and recognize the regulatory and safety considerations.
Summary
In a 26‑week trial, daily injections of 2 mg tesamorelin cut deep belly fat by about 15% and improved cholesterol and triglyceride levels in people with HIV, without major changes in blood sugar. The drug also boosted IGF‑I, showing strong growth‑hormone activity, and side effects were similar to placebo.
Abstract
Visceral adipose tissue accumulates during antiretroviral therapy in many patients who are infected with the human immunodeficiency virus (HIV); this process is associated with an increased cardiovascular risk. We assessed the use of a growth hormone-releasing factor analogue, tesamorelin, to decrease visceral adiposity. We randomly assigned 412 patients with HIV (86% of whom were men) who had an accumulation of abdominal fat to receive a daily subcutaneous injection of either 2 mg of tesamorelin or placebo for 26 weeks. The primary end point was the percent change from baseline in visceral adipose tissue as shown on computed tomography. Secondary end points included triglyceride levels, the ratio of total cholesterol to high-density lipoprotein (HDL) cholesterol, the level of insulin-like growth factor I (IGF-I), and self-assessed body image. Glycemic measures included glucose and insulin levels. The measure of visceral adipose tissue decreased by 15.2% in the tesamorelin group and increased by 5.0% in the placebo group; the levels of triglycerides decreased by 50 mg per deciliter and increased by 9 mg per deciliter, respectively, and the ratio of total cholesterol to HDL cholesterol decreased by 0.31 and increased by 0.21, respectively (P<0.001 for all comparisons). Levels of total cholesterol and HDL cholesterol also improved significantly in the tesamorelin group. Levels of IGF-I increased by 81.0% in the tesamorelin group and decreased by 5.0% in the placebo group (P<0.001). Adverse events did not differ significantly between the two study groups, but more patients in the tesamorelin group withdrew from the study because of an adverse event. No significant differences were observed in glycemic measures. Daily tesamorelin for 26 weeks decreased visceral fat and improved lipid profiles, effects that might be useful in HIV-infected patients who have treatment-associated central fat accumulation. (ClinicalTrials.gov number, NCT00123253 [ClinicalTrials.gov] .).
Study Information
pubmed
2007
2007-12-06T00:00:00.000Z
10.1056/nejmoa072375