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Completed

NCT Number: NCT00465426

HIV and Cardiovascular Risk

HIV-infected patients treated with combination antiretroviral therapy demonstrate metabolic abnormalities that may predispose them to cardiovascular disease. In HIV-infected patients we will investigate progression rates of cardiovascular disease and assess whether these progression rates are predicted by increased inflammatory indices.

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Key information

About this study

HIV-infected patients treated with combination antiretroviral (ARV) therapy increasingly demonstrate metabolic abnormalities, including dyslipidemia, insulin resistance and body composition abnormalities that may predispose them to cardiovascular disease (CVD). Initial studies suggest increased carotid intima-media thickness (IMT) and endothelial dysfunction in this population. Increased carotid IMT over time has been demonstrated in HIV-infected patients compared to control subjects. However, traditional risk factors, such as dyslipidemia, diabetes mellitus and body composition changes alone do not fully predict increased cardiovascular disease in HIV-infected patients. One possible explanation is increased inflammation, related directly to effects of ARV therapy or indirectly from changes in fat distribution. In preliminary studies, our group has shown that changes in fat distribution were highly predictive of TNF and IL-6, as well as adiponectin, and that specific inflammatory cytokines were related in cross-sectional studies to increased IMT. In the proposed study we will investigate using detailed methodologies the relationship between adipocytokine concentrations and subclinical atherosclerosis in both cross-sectional and longitudinal studies. We will determine in HIV-infected patients on ARVs for greater than 6 months, progression rates of IMT and whether progression rates are predicted by increased inflammatory indices, controlling for traditional risk factors, and body composition changes. We will test the hypothesis that inflammation, more than traditional risk factors and ARV use, mediates subclinical atherosclerotic disease in HIV-infected patients.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Inclusion criteria

for Group 1 (HIV-infected group)

  • Age greater than or equal to 18 and less than or equal to 65 years of age
  • HIV positive, on the same combination ARV regimen for > than 6 months, including but not limited to either 2 NRTIs and an NNRTI or PI, or a triple NRTI regimen
  • CD4 >350 cells/mm3

Inclusion criteria

for Group 2 (HIV Negative, Healthy Control, age and BMI matched to HIV subjects)

  • No history of HIV infection (negative HIV test)
  • Age greater than or equal to 18 and less than or equal to 65 years of age

Exclusion criteria

Exclusion criteria

for Group 1 (HIV-infected group)

  • Hgb < 10.0 g/dL, creatinine > 1.5 mg/dL, SGPT > 2.5x ULN
  • Use of glucocorticoid, testosterone, growth hormone or other anabolic agents within the past 6 months
  • New antiretroviral regimen within 6 months of study initiation
  • Active substance abuse
  • Medications known to affect glucose or body composition
  • Positive pregnancy test or recently pregnant within the past year or lactating
  • Presence of active cancers
  • Acute viral, bacterial or other infections (excluding HIV)
  • Weight loss in the past 3 months of greater than 10 pounds

Criteria for Group 2 (HIV Negative, Healthy Control, age and BMI matched to HIV subjects)

  • Hgb < 10.0 g/dL, creatinine > 1.5 mg/dL, SGPT > 2.5x ULN
  • Use of glucocorticoid, testosterone, growth hormone or other anabolic agents within the past 6 months.
  • Active substance abuse
  • Medications known to affect glucose or body composition
  • Positive pregnancy test or recently pregnant within the past year or lactating
  • Acute viral, bacterial or other infections
  • Weight loss in the past 3 months of greater than 10 pounds

Treatment and study plan

Primary outcomes

  1. Carotid Intima Media Thickness

    Time frame: 2 years

  2. Waist Circumference

    Time frame: 2 years

  3. Blood pressure

    Time frame: 2 years

  4. Lipid levels

    Time frame: 2 years

  5. Glucose

    Time frame: 2 years

Secondary outcomes

  1. Inflammatory markers

    Time frame: 2 years

  2. Visceral adiposity

    Time frame: 2 years

Sponsors and collaborators

Lead sponsor

Massachusetts General Hospital

Other

Collaborators

  • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Registry information

Official study title

Assessment of Cardiovascular Risk in HIV Patients

Important dates

Study start
2007
Primary completion
2011
Study completion
2011
First posted
Apr 25, 2007
Registry last updated
Oct 31, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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