Carotid Artery Thickness in HIV Infected and Uninfected Adults

Sponsor
National Institute of Allergy and Infectious Diseases (NIAID) (NIH)
Overall Status
Completed
CT.gov ID
NCT00007319
Collaborator
(none)
132
10
13.2

Study Details

Study Description

Brief Summary

The intima-media thickness (IMT) test is a low cost, non-invasive way to measure the thickness of the carotid artery (the large artery in the neck). The purpose of this study is to compare the thickness of the carotid artery among HIV infected adults taking protease inhibitors (PIs), HIV infected adults not taking PIs, and HIV uninfected adults, and to examine how the thickness may change over time.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Determination of clinical, lipid, and non-lipid risk factors has been the traditional approach for gauging an individual's risk for coronary artery disease (CAD). However, the IMT test, which uses sound waves to measure the thickness of the carotid artery, has been found to diagnose CAD and predict a person's risk for heart disease as well as or better than lipid and non-lipid risk factors. This study will use the IMT test to see if anti-HIV treatment and HIV infection affect a patient's risk of developing atherosclerosis (hardening of the arteries) by comparing carotid artery thickness among HIV infected adults taking PIs, HIV infected adults not taking PIs, and HIV uninfected adults.

    There are 3 groups in this study. Group 1 will comprise HIV infected participants currently taking a PI-containing regimen. Group 2 will comprise HIV infected participants who are not taking PIs. Group 3 will comprise HIV uninfected participants. At each site, participants will be enrolled by "triads" consisting of an individual from each group. Each member of the triad will be closely matched by gender, age, smoking and menopausal status, race, and normal or hypertensive blood pressure. All 3 members of the triad must be identified before participants are registered to the study.

    All participants will visit the clinic at Weeks 1, 24, 48, 72, 96, and 144 (3 years). At each visit, participants will have a physical exam, medical history and waist/hip ratio assessment, blood collection, and an IMT test. The absolute value for carotid IMT will be compared among the 3 groups. Viral load and CD4 counts will also be measured in Group 1 and 2 participants.

    Study Design

    Study Type:
    Observational
    Time Perspective:
    Prospective
    Official Title:
    Carotid Artery Intima-Media Thickness in HIV-Infected and Uninfected Adults: A Pilot Study

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      18 Years and Older
      Sexes Eligible for Study:
      All
      Accepts Healthy Volunteers:
      Yes

      Inclusion Criteria for Group 1

      • HIV infected

      • Have taken at least 1 PI continuously for 2 or more years and are currently taking at least 1 PI. Stopping therapy for 4 weeks or less for management of side effects or to change therapy is allowed.

      • Viral load of 10,000 copies/ml or less

      Inclusion Criteria for Group 2

      • HIV infected

      • Not currently receiving PIs or have not taken PIs in at least 3 months

      • Not planning to initiate PI therapy in the few months following study entry

      • Viral load of 10,000 copies/ml or less

      • If not currently on anti-HIV treatment, must have been on treatment for at least 6 months in the past

      Inclusion Criteria for Group 3

      • HIV uninfected

      Exclusion Criteria for All Groups

      • Diabetes or current use of oral medications for diabetes

      • Kidney disease

      • ALT or AST greater than 2.5 times the upper limit of normal

      • Hypothyroidism

      • Family history (parents, brothers, sisters, or children) of heart attacks before age 55 in males and age 65 in females

      • Alcohol or drug abuse

      • Pregnant or plan to become pregnant during the study

      • Body mass index (BMI) greater than 30

      • Systemic chemotherapy or radiation therapy

      • Systemic steroids (prednisone or equivalent) at doses greater than 5 mg/day for more than 30 consecutive days

      • History of coronary heart disease or stroke (including chest pain, heart attack, or abnormal stress test)

      • Uncontrolled hypertension

      Contacts and Locations

      Locations

      Site City State Country Postal Code
      1 Kaiser Foundation Hosp Harbor City California United States 90710
      2 Kaiser Permanente LAMC Los Angeles California United States 90027
      3 Univ of Southern California / LA County USC Med Ctr Los Angeles California United States 900331079
      4 UCLA CARE Ctr Los Angeles California United States 90095
      5 Univ of California, San Diego San Diego California United States 92103
      6 Harbor UCLA Med Ctr Torrance California United States 90502
      7 Univ of Hawaii Honolulu Hawaii United States 96816
      8 Univ of Minnesota Minneapolis Minnesota United States 55455
      9 Univ of Pennsylvania Philadelphia Pennsylvania United States 19104
      10 Univ of Washington Seattle Washington United States 98104

      Sponsors and Collaborators

      • National Institute of Allergy and Infectious Diseases (NIAID)

      Investigators

      • Study Chair: Judith S. Currier, MD, MSc, University of California, Los Angeles
      • Study Chair: Howard N. Hodis, MD, Atherosclerosis Research Unit, University of Southern California

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      Responsible Party:
      , ,
      ClinicalTrials.gov Identifier:
      NCT00007319
      Other Study ID Numbers:
      • ACTG A5078
      • AACTG A5078
      First Posted:
      Aug 31, 2001
      Last Update Posted:
      Sep 17, 2008
      Last Verified:
      May 1, 2006

      Study Results

      No Results Posted as of Sep 17, 2008