HIV Infections Clinical Trial
Official title:
The Effect of Low-Dose Human Growth Hormone Therapy in HIV Infected Patients on Highly Active Antiretroviral Therapy (HAART)
The purpose of this study is to investigate the effect of low-dose human growth hormone therapy on immune status and fat morphology.
Following the introduction of highly active antiretroviral therapy (HAART) in the
mid-nineties, the improvement in the clinical course of HIV has lead to a dramatic reduction
in morbidity and mortality. However, a growing concern has been the emergence of an
increasing number of drug therapy failure, mainly caused by rebounding virus. This effect in
turn is prompted respectively by developing resistance and failing compliance mainly due to
early or late adverse reactions. These adverse reactions mainly consists of a number of
metabolic and morphologic changes, known as HIV associated lipodystrophy syndrome (HALS) and
affects approximately 40 % of HIV infected patients on HAART. HALS is characterized by
lipoatrophy on extremities, gluteal and facial regions combined with intraabdominal
lipoaccumulation, "buffalo hump" and lipomas.
Thus, despite progress in the development of new drugs with new targets and resistance
profiles the need for agents with immune modulating properties is evident, both as a way to
overcome the problems of resistance and hopefully modify treatment regimens in order to
reduce the exposure to late adverse reactions caused by HAART. A number of studies have
addressed the problems of modulating the immune response during HIV infection. Results are
promising but a major obstacle seems to be adverse effects. In the pre-HAART era high dose
human growth hormone (hGH) therapy has been used for HIV wasting and in the HAART era the
impact on fat distribution in HIV infected patients have been investigated based on the
lipolytic properties of hGH. However high dosage of hGH has been associated with severe
adverse effects limiting the usefulness in daily clinical practice. One recent study
demonstrated increments in thymic mass and a rise in the number of circulating naïve CD4 T
cells upon treatment with high dose hGH. Our group has conducted a 60 week pilot study with
daily injection of 0.7 mg genotropin, demonstrating an immune stimulating effect as well as
an increased limb fat/truncal fat ratio, without metabolic and clinically recognizable side
effects. Based on these findings we plan to perform a randomized, double blind, prospective,
interventional study including 50 HIV infected patients on HAART, investigating the effect
of low dose hGH on immune status and fat distribution.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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