Evaluation of Vascular Event Risk while on Long-term Anti-retroviral Suppressive Therapy [EVERLAST]: Protocol for a

Fred Stephen Sarfo1,2, Michelle Nichols3, Mulugeta Gebregziabher3

  • 1Kwame Nkrumah University of Science & Technology, Kumasi, Ghana.

Eneurologicalsci
|April 24, 2019
PubMed

Insights

Cardiovascular disease (CVD) risk is elevated in people with HIV due to chronic inflammation and combination antiretroviral therapy (cART). The EVERLAST study in Ghana assesses CVD risk factors in HIV patients on ART, comparing them to uninfected and ART-naïve individuals.

Area of Science:

  • Cardiology
  • Infectious Diseases
  • Public Health

Background:

  • HIV infection accelerates atherosclerosis due to chronic inflammation.
  • Combination antiretroviral therapy (cART) may have adverse metabolic effects, increasing cardiovascular disease (CVD) risk.
  • Sub-Saharan Africa (SSA) has a high HIV burden but limited research on CVD risk in this population.

Purpose of the Study:

  • To characterize the burden of CVD among HIV patients on ART in Ghana.
  • To explore factors contributing to CVD risk in this population.
  • To compare CVD risk markers between HIV-positive patients on ART, HIV-positive ART-naïve individuals, and HIV-uninfected controls.

Main Methods:

  • Prospective study design with convergent mixed methods approach.
  • Evaluation of CVD risk using Carotid Intimal Media Thickness (CIMT) measurements.
  • Comparison of 240 HIV patients on ART with 240 HIV-uninfected and 240 HIV-positive ART-naïve controls.
  • Qualitative analysis of stakeholder perceptions regarding CVD risk in HIV patients.

Main Results:

  • Primary outcome: CIMT measured cross-sectionally and prospectively.
  • Secondary outcomes: CVD risk factors, CVD risk equations, neurocognitive dysfunction, and psychological well-being.
  • Analysis of ART exposure, lifestyle, traditional beliefs, and socio-economic indicators' impact on CVD risk.

Conclusions:

  • Findings will elucidate the contributions of ART and environmental factors to CVD risk in resource-limited settings.
  • Study results will inform the development of interventions for CVD risk management in SSA.
  • Evidence generated will guide future randomized controlled trials for CVD risk management in HIV patients.
Abstract

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