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Role of recombinant human growth hormone in HIV-Associated wasting and cachexia: Pathophysiology and rationale for treatment

Journal

CLINICAL THERAPEUTICS
Volume 29, Issue 11, Pages 2269-2288

Publisher

ELSEVIER
DOI: 10.1016/j.clinthera.2007.11.004

Keywords

HIV; cachexia; growth hormone

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Background: Wasting, or cachexia, is a significant, debilitating, and potentially life-threatening complication of HIV infection. It is associated with reduced strength and functional ability, reduced ability to withstand opportunistic infections, and increased risk of mortality. Although the incidence of HIV-associated wasting may have declined since the introduction of highly active antiretroviral therapy (HAART), it continues to be a concern in this patient population. Objective: This paper reviews available data on the etiology and clinical impact of HIV-associated wasting, the role of the growth hormone/insulin-like growth factor-I axis in the pathophysiology of this condition, and the rationale for its treatment with recombinant human growth hormone (rhGH). Methods: MEDLINE was searched for articles published in English through August 2007 using the terms HIV, wasting (and related terms), and growth hormone. Preference was given to clinical studies (including randomized clinical studies), meta-analyses, and guidelines. Review articles were evaluated and the bibliographies examined for additional relevant articles. The analysis was restricted to studies conducted in developed countries. Results: Alterations in the growth hormone/insulinlike growth factor-I axis have been observed in patients with HIV-associated wasting, including elevated levels of the former and reduced levels of insulin-like growth factor 1. In randomized, placebo-controlled studies, rhGH significantly improved lean body mass by similar to 3 kg compared with placebo (P < 0.001) and total body weight by similar to 3 kg (P < 0.001), and was associated with significant improvements in physical endurance and quality of life (P < 0.001). Common adverse events with rhGH therapy include blood glucose elevations, arthralgia (36.4%), myalgia (30.4%), and peripheral edema (26.1%), but these usually respond to dose reduction or drug discontinuation. Conclusions: Physicians should be alert to the possibility of wasting in HIV-infected patients receiving HAART and should consider treatment to improve patients' stamina and quality of life. The evidence supports a role for rhGH in the treatment of patients with HIV-associated wasting. Regular blood glucose monitoring is advised when treating wasting with rhGH. (Clin Ther. 2007;29:2269-2288) Copyright (c) 2007 Excerpta Medica, Inc.

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