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
2017 pubmed 8 citations

Fibroblast growth factor 21 decreases after liver fat reduction via growth hormone augmentation.

Braun. Laurie R LR; Feldpausch. Meghan N MN; Czerwonka. Natalia N; Torriani. Martin M; Grinspoon. Steven K SK; Stanley. Takara L TL

Key Findings

  • Tesamorelin reduced liver fat in HIV‑infected participants over six months
  • Serum FGF21 levels fell alongside liver‑fat reduction, contrary to expectations that GH raises FGF21
  • Reductions in FGF21 correlated with better liver enzymes (GGT) and fibrosis score (FIB4)

Practical Outcomes

  • Tesamorelin may be a useful tool for lowering liver fat, but it’s a prescription drug studied only in HIV patients, so off‑label use requires medical oversight. The typical protocol was 2 mg daily for six months, with monitoring of liver fat via imaging and blood markers. Expect liver‑fat improvements without needing to boost FGF21, indicating other metabolic pathways are involved.

Summary

In a study of HIV‑positive adults, daily tesamorelin (2 mg) for six months lowered liver fat and also reduced the hormone FGF21, which usually rises when the liver is fatty. The drop in FGF21 tracked with improvements in liver health markers, showing that tesamorelin’s liver‑fat‑cutting effect isn’t because it raises FGF21. This suggests growth‑hormone‑boosting can improve liver health through other pathways.

Abstract

Fibroblast growth factor 21 (FGF21) ameliorates steatohepatitis but is increased in humans with fatty liver, potentially due to compensatory mechanisms and/or FGF21 resistance. Further, animal models suggest that GH increases serum FGF21. Tesamorelin, a growth hormone releasing hormone agonist, reduces liver fat in HIV-infected individuals. The objectives of this study were to investigate changes in FGF21 during tesamorelin treatment, to elucide the interplay between FGF21, GH augmentation, and liver fat reduction in humans. 50 HIV-infected men and women with increased abdominal adiposity participated in this randomized, placebo-controlled trial of tesamorelin, 2mg vs. identical placebo daily for six months. Fasting laboratory measures, liver fat by <sup>1</sup>H-magnetic resonance spectroscopy, and visceral adipose tissue (VAT) by computed tomography were obtained. Euglycemic hyperinsulinemic clamp was performed in a randomly selected subset. At baseline, serum log<sub>10</sub> FGF21 was significantly associated with log<sub>10</sub> liver fat (r=0.32, p=0.03). Log<sub>10</sub> FGF21 tended to decrease in the tesamorelin group compared to placebo (p=0.06). Among the entire cohort, reductions in FGF21 were significantly associated with reductions in liver fat (&#x3c1;=0.41, p=0.01), log<sub>10</sub> gamma glutamyl tran speptidase (GGT, r=0.40, p=0.009), and FIB4 index (r=0.37, p=0.02). In HIV-infected individuals, FGF21 is significantly positively associated with liver fat. FGF21 decreases in association with reductions in liver fat, GGT, and FIB4, suggesting that FGF21 is upregulated in the context of steatosis and steatohepatitis and is reduced when these conditions improve. Moreover, these data suggest that tesamorelin improves liver fat via pathways other than increasing serum FGF21. clinicaltrials.govNCT01263717.

Study Information

Provider

pubmed

Year

2017

Date

2017-10-07T00:00:00.000Z

DOI

10.1016/j.ghir.2017.10.002

Citations

8

References

49