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Randomized, Placebo-Controlled Study of Leptin for the Treatment of HIV Lipodystrophy and Metabolic Syndrome

Primary Purpose

HAART-induced Lipodystrophy and Metabolic Syndrome

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
r-metHuLeptin
Placebo
Sponsored by
Beth Israel Deaconess Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for HAART-induced Lipodystrophy and Metabolic Syndrome focused on measuring leptin, lipodystrophy, insulin resistance, hyperlipidemia, metabolic syndrome

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: At least 18 years old Documented HIV infection Exposed to at least 6 months of cumulative highly active antiretroviral medications for HIV Developed fat depletion after starting HIV medications Low leptin level in the blood Fasting triglyceride level > 300 mg/dl Exclusion Criteria: Active infectious diseases, except HIV Diabetes prior to starting HIV medications Alcohol or drug abuse Triglyceride level > 1000 mg/dl Significant kidney, liver, or thyroid dysfunction Cancer or lymphoma Pregnancy or planning to become pregnant during the study

Sites / Locations

  • Beth Israel Deaconess Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

r-MetHuLeptin

Placebo

Arm Description

r-MetHuLeptin SubQ once daily

SubQ once daily

Outcomes

Primary Outcome Measures

Serum Lipid Levels

Secondary Outcome Measures

Insulin Resistance (as Assessed by HOMA-IR)
Glycemia (as Assessed by Fasting Glucose)
Low Density Lipoprotein (LDL) Cholesterol Levels
Free Fatty Acid (FFA) Levels
Blood Pressure
percent change in mean blood pressure
Fibrinogen
Fibrinogen
Insulin Levels
Lean Body Mass
lean body mass
Viral Load
CD4+ Lymphocytes
Interleukin-6 (IL-6) Levels
Hepatic Fat Content

Full Information

First Posted
August 30, 2005
Last Updated
April 6, 2017
Sponsor
Beth Israel Deaconess Medical Center
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), Amgen
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1. Study Identification

Unique Protocol Identification Number
NCT00140244
Brief Title
Randomized, Placebo-Controlled Study of Leptin for the Treatment of HIV Lipodystrophy and Metabolic Syndrome
Official Title
Role of Leptin in Highly Active Antiretroviral Therapy (HAART)-Induced Lipodystrophy and Metabolic Syndrome in HAART-Treated HIV Patients
Study Type
Interventional

2. Study Status

Record Verification Date
April 2017
Overall Recruitment Status
Completed
Study Start Date
December 2001 (undefined)
Primary Completion Date
June 2011 (Actual)
Study Completion Date
June 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Beth Israel Deaconess Medical Center
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), Amgen

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to examine whether replacing leptin to normal levels can reverse the changes in fat distribution, lipid profile, and other metabolic problems associated with highly active antiretroviral therapy (HAART)-induced lipodystrophy and metabolic syndrome in HIV patients.
Detailed Description
Exposure to HIV medications has been associated with metabolic changes including generalized fat depletion (lipoatrophy), high triglyceride levels, and in some patients, high sugar levels or diabetes. This syndrome is associated with a deficiency of leptin, a hormone produced by fat cells. Recent studies involving leptin administration to patients with congenital lipoatrophy have shown dramatic improvements in metabolic parameters such as insulin resistance and hyperlipidemia. Leptin administration to patients with HAART-induced lipoatrophy may also lead to significant improvements in the metabolic abnormalities found in these HIV+ patients. The aims of this study are to examine the effect of leptin administration on insulin resistance and other parameters of the metabolic syndrome in HIV patients with HAART-induced lipoatrophy. Comparison: Leptin-treated group to placebo-treated group

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HAART-induced Lipodystrophy and Metabolic Syndrome
Keywords
leptin, lipodystrophy, insulin resistance, hyperlipidemia, metabolic syndrome

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
7 (Actual)

8. Arms, Groups, and Interventions

Arm Title
r-MetHuLeptin
Arm Type
Active Comparator
Arm Description
r-MetHuLeptin SubQ once daily
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
SubQ once daily
Intervention Type
Drug
Intervention Name(s)
r-metHuLeptin
Intervention Type
Drug
Intervention Name(s)
Placebo
Primary Outcome Measure Information:
Title
Serum Lipid Levels
Time Frame
At the end of each two month intervention
Secondary Outcome Measure Information:
Title
Insulin Resistance (as Assessed by HOMA-IR)
Time Frame
At the end of each two month intervention
Title
Glycemia (as Assessed by Fasting Glucose)
Time Frame
At the end of each two month intervention
Title
Low Density Lipoprotein (LDL) Cholesterol Levels
Time Frame
At the end of each two month intervention
Title
Free Fatty Acid (FFA) Levels
Time Frame
At the end of each two month intervention
Title
Blood Pressure
Description
percent change in mean blood pressure
Time Frame
At the end of each two month intervention
Title
Fibrinogen
Description
Fibrinogen
Time Frame
At the end of each two month intervention
Title
Insulin Levels
Time Frame
At the end of each two month intervention
Title
Lean Body Mass
Description
lean body mass
Time Frame
At the end of each two month intervention
Title
Viral Load
Time Frame
At the end of each two month intervention
Title
CD4+ Lymphocytes
Time Frame
At the end of each two month intervention
Title
Interleukin-6 (IL-6) Levels
Time Frame
At the end of each two month intervention
Title
Hepatic Fat Content
Time Frame
At the end of each two month intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: At least 18 years old Documented HIV infection Exposed to at least 6 months of cumulative highly active antiretroviral medications for HIV Developed fat depletion after starting HIV medications Low leptin level in the blood Fasting triglyceride level > 300 mg/dl Exclusion Criteria: Active infectious diseases, except HIV Diabetes prior to starting HIV medications Alcohol or drug abuse Triglyceride level > 1000 mg/dl Significant kidney, liver, or thyroid dysfunction Cancer or lymphoma Pregnancy or planning to become pregnant during the study
Facility Information:
Facility Name
Beth Israel Deaconess Medical Center
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02215
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
35820631
Citation
Bouzoni E, Perakakis N, Connelly MA, Angelidi AM, Pilitsi E, Farr O, Stefanakis K, Mantzoros CS. PCSK9 and ANGPTL3 levels correlate with hyperlipidemia in HIV-lipoatrophy, are regulated by fasting and are not affected by leptin administered in physiologic or pharmacologic doses. Metabolism. 2022 Sep;134:155265. doi: 10.1016/j.metabol.2022.155265. Epub 2022 Jul 9.
Results Reference
derived
PubMed Identifier
21081243
Citation
Magkos F, Brennan A, Sweeney L, Kang ES, Doweiko J, Karchmer AW, Mantzoros CS. Leptin replacement improves postprandial glycemia and insulin sensitivity in human immunodeficiency virus-infected lipoatrophic men treated with pioglitazone: a pilot study. Metabolism. 2011 Jul;60(7):1045-9. doi: 10.1016/j.metabol.2010.10.002. Epub 2010 Nov 16.
Results Reference
derived
Links:
URL
http://www.bidmc.org/
Description
Click here for more information about Beth Israel Deaconess Medical Center.

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Randomized, Placebo-Controlled Study of Leptin for the Treatment of HIV Lipodystrophy and Metabolic Syndrome

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