Human immunodeficiency virus 1 infection, cocaine, and coronary calcification

Shenghan Lai1, Joao A C Lima, Hong Lai

  • 1Department of Pathology, The Johns Hopkins Medical Institutions, Baltimore, MD 21287, USA. slai@jhmi.edu

Insights

Cocaine use and human immunodeficiency virus (HIV) infection, individually or combined, are associated with coronary calcification, an early sign of cardiovascular disease. This study highlights the increased risk in individuals with both HIV and cocaine use.

Area of Science:

  • Cardiovascular disease research
  • Infectious disease epidemiology
  • Substance abuse research

Background:

  • Clinical cardiovascular disease is linked to cocaine use and HIV infection.
  • Effects on subclinical disease, particularly combined use, are underreported.
  • Coronary calcification is a key marker for subclinical atherosclerosis.

Purpose of the Study:

  • To evaluate the association of cocaine use and HIV infection with coronary calcification.
  • To determine if combined HIV and cocaine use increases subclinical atherosclerosis risk.
  • To assess individual and combined effects on early cardiovascular disease markers.

Main Methods:

  • An observational study enrolled 224 Black participants in Baltimore.
  • Data collected via interviews, clinical exams, echocardiography, lipid profiles, hs-CRP, and CT scans for coronary calcium.
  • Cross-sectional analysis of data collected between May 2000 and March 2003.

Main Results:

  • Coronary calcification was most prevalent in the HIV-positive and cocaine-positive group (37.6%).
  • Both HIV infection and cocaine use were independently associated with coronary calcification after adjusting for multiple risk factors.
  • Univariate analysis showed significant associations between HIV, cocaine use, and markers of coronary calcification.

Conclusions:

  • HIV infection, cocaine use, or their combination contribute to early subclinical atherosclerotic cardiovascular disease.
  • Findings underscore the importance of screening for cardiovascular risk in these populations.
  • Further research is needed to elucidate mechanisms and long-term outcomes.
Abstract

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