The Effect of Low-Dose Human Growth Hormone Therapy in HIV Infected Patients
Information source: Hvidovre University Hospital
Information obtained from ClinicalTrials.gov on March 21, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: HIV Infections; Lipodystrophy
Intervention: Genotropin (Drug)
Phase: Phase 4
Status: Active, not recruiting
Sponsored by: Hvidovre University Hospital Official(s) and/or principal investigator(s): Birgitte R Hansen, MD, Principal Investigator, Affiliation: Unaffiliated
Summary
The purpose of this study is to investigate the effect of low-dose human growth hormone
therapy on immune status and fat morphology.
Clinical Details
Official title: The Effect of Low-Dose Human Growth Hormone Therapy in HIV Infected Patients on Highly Active Antiretroviral Therapy (HAART)
Study design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study
Primary outcome: Impact of hGH 0.7 mg/day on number of mature and naïve CD4 cells in HIV patients at 9 months
Secondary outcome: Impact of hGH 0.7 mg/day at 9 months on:thymic size fat distribution as measured with CT and DEXA scans glucose metabolism i.e.glucose tolerance, insulin sensitivity and beta cell function as measured by OGTT insulin sensitivity as measured by hyperinsulinaemic euglycaemic clamp lipid profile quality of life and adherence to HAART cytokines safety parameters
Detailed description:
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.
Eligibility
Minimum age: 21 Years.
Maximum age: 60 Years.
Gender(s): Male.
Criteria:
Inclusion Criteria:
- Male
- Caucasian race
- Age >21 years, <60 years
- HIV-1 infection
- HAART treated > 12 months
- HIV-RNA < 100 copies/ml
- CD4 count > 200
- Fasting plasma glucose < 6. 1 mM
- Stable weight
Exclusion Criteria:
- BMI > 28 kg/m2 and BMI < 18. 5 kg/m2
- Wasting or AIDS defining disease
- Severe chronic diseases other than HIV
- Cancer, previous transplantation
- Previous AMI
- Diabetes
- Hormonal substitution therapy
- Lipid lowering or antidiabetic therapy within 3 months
- Abuse of narcotics or alcohol
- Major psychiatric disorders
- Adverse reactions towards Genotropin
- Calcium-ion < 1. 15 or > 1. 35 mM
- D-vitamin < 19 nM
- TSH < 0. 1 or > 10 mIU/l
Locations and Contacts
Clinical Research Unit, Hvidovre University Hospital, Hvidovre 2650, Denmark
Additional Information
Clinical Research Department Hvidovre University Hospital
Related publications: Andersen O, Haugaard SB, Hansen BR, Orskov H, Andersen UB, Madsbad S, Iversen J, Flyvbjerg A. Different growth hormone sensitivity of target tissues and growth hormone response to glucose in HIV-infected patients with and without lipodystrophy. Scand J Infect Dis. 2004;36(11-12):832-9. Haugaard SB, Andersen O, Dela F, Holst JJ, Storgaard H, Fenger M, Iversen J, Madsbad S. Defective glucose and lipid metabolism in human immunodeficiency virus-infected patients with lipodystrophy involve liver, muscle tissue and pancreatic beta-cells. Eur J Endocrinol. 2005 Jan;152(1):103-12. Haugaard SB, Andersen O, Volund A, Hansen BR, Iversen J, Andersen UB, Nielsen JO, Madsbad S. Beta-cell dysfunction and low insulin clearance in insulin-resistant human immunodeficiency virus (HIV)-infected patients with lipodystrophy. Clin Endocrinol (Oxf). 2005 Mar;62(3):354-61. Haugaard SB, Andersen O, Hansen BR, Andersen UB, Volund A, Iversen J, Nielsen JO, Madsbad S. In nondiabetic, human immunodeficiency virus-infected patients with lipodystrophy, hepatic insulin extraction and posthepatic insulin clearance rate are decreased in proportion to insulin resistance. Metabolism. 2005 Feb;54(2):171-9. Haugaard SB, Andersen O, Hansen BR, Orskov H, Andersen UB, Madsbad S, Iversen J, Flyvbjerg A. Insulin-like growth factors, insulin-like growth factor-binding proteins, insulin-like growth factor-binding protein-3 protease, and growth hormone-binding protein in lipodystrophic human immunodeficiency virus-infected patients. Metabolism. 2004 Dec;53(12):1565-73. Andersen O, Haugaard SB, Flyvbjerg A, Andersen UB, Orskov H, Madsbad S, Nielsen JO, Iversen J. Low-dose growth hormone and human immunodeficiency virus-associated lipodystrophy syndrome: a pilot study. Eur J Clin Invest. 2004 Aug;34(8):561-8.
Starting date: February 2005
Ending date: April 2008
Last updated: March 7, 2007
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