Plasma acylcarnitines and progression of carotid artery atherosclerosis in HIV infection

  • Simin Hua
  • , Justin M. Scott
  • , David B. Hanna
  • , Sabina A. Haberlen
  • , Sanjiv J. Shah
  • , Howard N. Hodis
  • , Alan L. Landay
  • , Jason M. Lazar
  • , Jorge R. Kizer
  • , Bing Yu
  • , Wendy S. Post
  • , Kathryn Anastos
  • , Robert C. Kaplan
  • , Clary B. Clish
  • , Qibin Qi

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

To evaluate plasma acylcarnitine profiles and their relationships with progression of carotid artery atherosclerosis among individuals with and without HIV infection.Design:Prospective cohort studies of 499 HIV-positive and 206 HIV-negative individuals from the Women's Interagency HIV Study and the Multicenter AIDS Cohort Study.Methods:Twenty-four acylcarnitine species were measured in plasma samples of participants at baseline. Carotid artery plaque was assessed using repeated B-mode carotid artery ultrasound imaging in 2004-2013. We examined the associations of individual and aggregate short-chain (C2-C7), medium-chain (C8-C14) and long-chain acylcarnitines (C16-C26) with incident carotid artery plaque over 7 years.Results:Among 24 acylcarnitine species, C8-carnitines and C20:4-carnitines showed significantly lower levels comparing HIV-positive to HIV-negative individuals (false discovery rate adjusted P<0.05); and C20-carnitines and C26-carnitines showed significantly higher levels in HIV positive using antiretroviral therapy than those without antiretroviral therapy (false discovery rate adjusted P<0.05). In the univariate analyses, higher aggregated short-chain and long-chain acylcarnitine scores were associated with increased risk of carotid artery plaque [risk ratios (RRs)=1.22 (95% confidence interval 1.02-1.45) and 1.20 (1.02-1.41) per SD increment, respectively]. The association for the short-chain acylcarnitine score remained significant [RR=1.23 (1.05-1.44)] after multivariate adjustment (including traditional cardiovascular disease risk factors). This association was more evident in HIV-positive individuals without persistent viral suppression [RR=1.37 (1.11-1.69)] compared with those with persistent viral suppression during follow-up [RR=1.03 (0.76-1.40)] or HIV-negative individuals [RR=1.02 (0.69-1.52)].Conclusion:In two HIV cohorts, plasma levels of most acylcarnitines were not significantly different between HIV-positive and HIV-negative individuals. However, higher levels of aggregated short-chain acylcarnitines were associated with progression of carotid artery atherosclerosis.

Original languageEnglish (US)
Pages (from-to)1043-1052
Number of pages10
JournalAIDS
Volume33
Issue number6
DOIs
StatePublished - May 1 2019
Externally publishedYes

Keywords

  • HIV infection
  • acylcarnitines
  • atherosclerosis
  • cardiovascular disease
  • carotid artery
  • metabolomics

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology
  • Infectious Diseases

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