Overview

Eplerenone in HIV Associated Abdominal Fat Accumulation

Status:
Completed
Trial end date:
2017-11-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to test the effects of a drug, eplerenone, along with lifestyle modification to affect sugar metabolism, body fat distribution, and cardiovascular health in HIV-infected individuals. In non-HIV-infected individuals, recent data has shown that aldosterone, a hormone that regulates salt and water balance, is increased in association with increased belly fat and decreased insulin sensitivity. In HIV-infected individuals, aldosterone appears to be higher in individuals with increased belly fat, and increased aldosterone appears to be strongly associated with impaired sugar metabolism. In this study, the investigators will test the effects of eplerenone, which is a medication that blocks the actions of aldosterone, along with lifestyle modification. The investigators hypothesize that eplerenone may improve sugar metabolism, improve markers of cardiovascular health, and reduce fat accumulation in liver and muscle.
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Massachusetts General Hospital
Treatments:
Eplerenone
Spironolactone
Criteria
Inclusion Criteria:

1. Increased waist circumference based on NCEP guidelines (>102cm in men and >88cm in
women) and impaired glucose tolerance (either IFG > 100 mg/dL but < 126 mg/dL or 2hr
glucose > 140 mg/dl but < 200 mg/dL, or fasting insulin >12 uIU/mL)

2. HIV positive for 5y and on a stable ART regimen for at least 12 months

3. Age ≥ 30 and ≤ 65 years of age

Exclusion Criteria:

1. ACE Inhibitor, ARB, verapamil, or spironolactone

2. Potassium supplementation

3. Estimated GFR<60, creatinine > 1.5 mg/dL

4. Serum K > 5.5 mEq/L, ALT > 2.5 times the upper limit of normal, Hgb < 11g/dL

5. Uncontrolled hypertension (SBP ≥ 160 or DBP ≥ 100)

6. Current or prior steroid use within past 6 months

7. Known history of diabetes mellitus or current use of anti-diabetic medications

8. Concomitant use of full dose ritonavir, nelfinavir, clarithromycin and other strong
inhibitors of CYP34A

9. Use of St. John's Wart (CYP3A4 inducer)

10. Pregnant or actively seeking pregnancy, breastfeeding

11. For women: Pregnant or actively seeking pregnancy, breastfeeding, failure to use an
acceptable non-hormonal form of birth control, including abstinence, barrier
contraceptives, or non-hormonal IUD.

12. Estrogen or progestational derivative use within 3 months

13. Testosterone use for non-physiologic purposes, or physiologic testosterone replacement
for < 3 months.

14. Current growth hormone or growth hormone releasing hormone use

15. Current viral, bacterial or other infections (excluding HIV)

16. Current active substance abuse

17. Patients with a significant history of cardiovascular disease, including prior MI or
stroke