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Observational Study
. 2019 Aug 22;14(8):e0219710.
doi: 10.1371/journal.pone.0219710. eCollection 2019.

Association between alcohol use and inflammatory biomarkers over time among younger adults with HIV-The Russia ARCH Observational Study

Affiliations
Observational Study

Association between alcohol use and inflammatory biomarkers over time among younger adults with HIV-The Russia ARCH Observational Study

Kaku A So-Armah et al. PLoS One. .

Abstract

Background: Biomarkers of monocyte activation (soluble CD14 [sCD14]), inflammation (interleukin-6 [IL-6]), and altered coagulation (D-dimer) are associated with increased mortality risk in people with HIV. The objective of the Russia Alcohol Research Collaboration on HIV/AIDS (ARCH) study was to evaluate the association between heavy alcohol use and inflammatory biomarkers over time.

Methods: The study sought antiretroviral therapy naive participants with HIV (n = 350) and assessed them at baseline, 12 and 24 months. Linear mixed effects models were used to determine whether heavy drinking (self-report augmented by phosphatidylethanol [PEth], an alcohol biomarker) was longitudinally associated with IL-6, sCD14 and D-dimer adjusting for potential confounders (e.g., demographics, HIV factors, comorbid conditions).

Results: Participants' baseline characteristics were as follows: 71% male; mean age of 34 years; 87% self-reported hepatitis C; and 86% current smokers. Mean log10 (HIV RNA) was 4.3 copies/mL. Heavy alcohol use, based on National Institute of Alcohol Abuse and Alcoholism risky drinking criteria and PEth (versus non-heavy alcohol use) was associated with higher sCD14 (adjusted mean difference 125 ng/mL [95% CI: 42, 209]), IL-6 (ratio of means 1.35 [95% CI: 1.17, 1.55] pg/mL), and D-dimer (ratio of means 1.20 [95% CI: 1.06, 1.37] ug/mL) across the two-year follow-up.

Conclusion: Among HIV+ adults, current heavy alcohol use is associated with higher sCD14, IL-6 and D-dimer over time. Since these biomarkers are associated with mortality, interventions to mitigate effects of heavy drinking on these immune processes merit consideration.

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Conflict of interest statement

An employee of the funder (K. Bryant) is a co-author on this manuscript and helped guide analysis, interpretation and presentation of data and participated in the decision to submit the manuscript for publication. Debbie Cheng serves on Data Safety Monitoring Boards for Janssen Research & Development. This does not alter our adherence to PLOS ONE policies on sharing data and materials. The remaining authors report no declarations of interest.

Figures

Fig 1
Fig 1. Distribution of soluble CD14 (above) interleukin-6 (middle) and D-dimer (below) by heavy drinking status at baseline 12 and 24 months.
Fig 2
Fig 2. Distribution of soluble CD14 (above), interleukin-6 (middle) and D-dimer (below) by drinks per week.
Fig 3
Fig 3. Predicted values from piecewise linear mixed effects models evaluating the association between self-reported drinks per week and sCD14.
Separate slopes (95% confidence intervals) are reported for alcohol consumption of less than or equal to 25 drinks/week in the past month vs. consumption of greater than 25 drinks/week in the past month.
Fig 4
Fig 4. Predicted values from piecewise linear mixed effects models evaluating the association between self-reported drinks per week and IL-6.
Separate slopes (95% confidence intervals) are reported for alcohol consumption of less than or equal to 25 drinks/week.
Fig 5
Fig 5. Predicted values from linear mixed effects models evaluating the association between self-reported drinks per week and D-dimer.
Fig 6
Fig 6. Predicted values from linear mixed effects models evaluating the association between PEth and sCD14.
Fig 7
Fig 7. Predicted values from linear mixed effects models evaluating the association between PEth and IL-6.
Fig 8
Fig 8. Predicted values from linear mixed effects models evaluating the association between PEth and D-dimer.

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