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Association of Macrophage Inflammation Biomarkers With Progression of Subclinical Carotid Artery Atherosclerosis in HIV-Infected Women and Men
- Hanna, David B;
- Lin, Juan;
- Post, Wendy S;
- Hodis, Howard N;
- Xue, Xiaonan;
- Anastos, Kathryn;
- Cohen, Mardge H;
- Gange, Stephen J;
- Haberlen, Sabina A;
- Heath, Sonya L;
- Lazar, Jason M;
- Liu, Chenglong;
- Mack, Wendy J;
- Ofotokun, Igho;
- Palella, Frank J;
- Tien, Phyllis C;
- Witt, Mallory D;
- Landay, Alan L;
- Kingsley, Lawrence A;
- Tracy, Russell P;
- Kaplan, Robert C
- et al.
Published Web Location
https://doi.org/10.1093/infdis/jix082Abstract
Background
Monocytes and monocyte-derived macrophages promote atherosclerosis through increased inflammation and vascular remodeling. This may be especially true in chronic human immunodeficiency virus (HIV) infection.Methods
We examined 778 women (74% HIV+) in the Women's Interagency HIV Study and 503 men (65% HIV+) in the Multicenter AIDS Cohort Study who underwent repeated B-mode carotid artery ultrasound imaging in 2004-2013. We assessed baseline associations of the serum macrophage inflammation markers soluble (s)CD163, sCD14, galectin-3 (Gal-3), and Gal-3 binding protein (Gal-3BP) with carotid plaque formation (focal intima-media thickness >1.5 mm) over 7 years.Results
Marker levels were higher in HIV+ persons versus HIV- persons. Presence of focal plaque increased over time: from 8% to 15% in women, and 24% to 34% in men. After adjustment for demographic, behavioral, and cardiometabolic factors, and CRP and interleukin-6, each standard deviation increase in sCD14 was associated with increased plaque formation (risk ratio [RR] 1.24, 95% confidence interval [CI] 1.07-1.43). This pattern was consistentby sex. sCD163 was associated with plaque formation in virally suppressed HIV+ men (RR 1.52, 95% CI 1.04-2.22); Gal-3BP and Gal-3 were not associated with increased plaque.Conclusions
sCD14 and sCD163 may play important roles in atherogenesis among HIV+ persons.Many UC-authored scholarly publications are freely available on this site because of the UC's open access policies. Let us know how this access is important for you.