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Tesamorelin

Egrifta, TH9507

Quick Stats
Studies 64
Trials 24
Score 3
2008 pubmed 38 citations

Approach to the human immunodeficiency virus-infected patient with lipodystrophy.

Brown. Todd T TT

Key Findings

  • Lipodystrophy in HIV splits into fat loss (lipoatrophy) and fat gain (lipohypertrophy) with different causes and treatments
  • Switching to less toxic antiretroviral regimens can partially improve fat loss and lipid problems
  • GH‑axis therapies (e.g., tesamorelin) are promising for reducing central fat, while thiazolidinediones may aid sub‑cutaneous fat restoration

Practical Outcomes

  • Consider adjusting your HIV drug regimen to a less lipodystrophy‑prone combo, add lifestyle changes or surgery for belly fat, and explore GH‑axis agents like tesamorelin for central fat reduction. If you have lipoatrophy, thiazolidinediones might be a better first‑line diabetes drug than metformin.

Summary

HIV patients on modern drug combos often get weird fat changes – losing fat under the skin and gaining it around the belly – plus bad cholesterol and insulin issues. These problems come from the meds, the virus, and personal factors. Changing to gentler HIV drugs, diet/exercise or surgery, and new hormones that act on the growth‑hormone system can help, while some diabetes drugs (like thiazolidinediones) might be better than metformin for those losing sub‑cutaneous fat.

Abstract

Subcutaneous atrophy and central fat accumulation are common among HIV-infected patients receiving highly active antiretroviral therapy, and may be accompanied by dyslipidemia and insulin resistance. These fat changes, although commonly referred to together as lipodystrophy, are best considered as separate disorders, with distinct pathogeneses and treatment approaches. These morphological and metabolic abnormalities first appeared after introduction of protease inhibitors more than 10 yr ago, but research has demonstrated that their pathogenesis is multifactorial, with contributions from other antiretroviral medications, patient-related factors, and HIV itself. Switching to a less toxic highly active antiretroviral therapy regimen has shown partial effectiveness for the management of fat atrophy and lipid abnormalities. Lifestyle modification or surgical approaches are the treatment of choice for lipohypertrophy, although novel therapies targeting the GH axis show promise. HIV-related dyslipidemia may be difficult to treat, and can be complicated by drug-drug interactions between some lipid-lowering medications and antiretroviral medications. Treatment of diabetes in HIV-infected patients should generally follow established guidelines, but thiazolidinediones, rather than metformin, may be considered first-line treatment in a patient with lipoatrophy, given their potential to increase sc fat. The contribution of body fat changes and metabolic abnormalities to cardiovascular risk and the changing risk profiles of newer antiretroviral regimens are under intense investigation.

Study Information

Provider

pubmed

Year

2008

Date

2008-08-01T00:00:00.000Z

DOI

10.1210/jc.2008-1019

Citations

38

References

108