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    Open forum infectious diseases. 2017 Dec 22. doi: 10.1093/ofid/ofx275. pii: ofx275. pmc: PMC5772402
    Association of Suboptimal Antiretroviral Therapy Adherence With Inflammation in Virologically Suppressed Individuals Enrolled in the SMART Study.
    Castillo-Mancilla JR1,  Phillips AN2,  Neaton JD3,  Neuhaus J4,  Collins S5,  Mannheimer S6,  Pett S7,  Touzeau-Römer V8,  Polizzotto MN9,  Lundgren JD10,  Gardner EM11
    Author information
    1University of Colorado-AMC, Medicine/Infectious Diseases, Aurora, Colorado.
    2Institute for Global Health, University College London, London, UK.
    3University of Minnesota, School of Public Health, Minneapolis, Minnesota.
    4University of Minnesota, School of Public Health, Minneapolis, Minnesota.
    5HIV i-Base, London, UK.
    6Columbia University Medical Center, Harlem Hospital Center, New York, New York.
    7University College London, London, UK.
    8University of Vienna Medical School, AKH, Division of Immunology, Allergy and Infectious Diseases, Vienna, Austria.
    9Kirby Institute, University of New South Wales, Sydney, Australia.
    10CHIP, Department of Infectious Diseases, Rigshospitalet, Copenhagen, Denmark.
    11Denver Health Medical Center, Denver, Colorado.
    Abstract

    Suboptimal (ie, <100%) antiretroviral therapy (ART) adherence has been associated with heightened inflammation in cohort studies, even among people with virologic suppression. We aimed to evaluate this association among participants in the Strategies for Management of Antiretroviral Therapy (SMART) study who had virologic suppression (HIV-1 VL < 200 copies/mL) at enrollment. Based on self-reported adherence (7-day recall), plasma concentrations of interleukin 6 and D-dimer were 9% (95% confidence interval [CI], 1%-18%; P = .02) and 11% (95% CI, 1%-22%; P = .03) higher in participants who reported suboptimal vs 100% adherence, respectively. These findings confirm previous observations and support the hypothesis that suboptimal ART adherence, even in the context of virologic suppression, may have significant biological consequences. ClinicalTrials.gov number NCT00027352.


    KEYWORDS: SMART study, adherence, antiretroviral therapy, inflammation

    Publikations ID: 29362724
    Quelle: öffnen
     
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