Circulating biomarker correlates of left atrial size and myocardial extracellular volume fraction among persons living with and without HIV

Infection with human immunodeficiency virus (HIV) is associated with higher risk for myocardial disease despite modern combination antiretroviral therapy (cART). Factors contributing to this excess risk, however, remain poorly characterized. We aimed to assess cross-sectional relationships between e...

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Veröffentlicht in:BMC cardiovascular disorders 2022-09, Vol.22 (1), p.393-393, Article 393
Hauptverfasser: Peterson, Tess E, Landon, Christian, Haberlen, Sabina A, Bhondoekhan, Fiona, Plankey, Michael W, Palella, Frank J, Piggott, Damani A, Margolick, Joseph B, Brown, Todd T, Post, Wendy S, Wu, Katherine C
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Sprache:eng
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Zusammenfassung:Infection with human immunodeficiency virus (HIV) is associated with higher risk for myocardial disease despite modern combination antiretroviral therapy (cART). Factors contributing to this excess risk, however, remain poorly characterized. We aimed to assess cross-sectional relationships between elevations of left atrial volume index (LAVI) and myocardial extracellular volume (ECV) fraction that have been reported in persons living with HIV and levels of circulating biomarkers of inflammation, fibrosis, and myocyte stretch among persons living with and without HIV (PLWH, PLWOH). Participants from three cohorts of PLWH and PLWOH underwent cardiovascular magnetic resonance imaging for measurement of LAVI and ECV. Levels of circulating proteins (IL-6, sCD14, galectin-3, NT-proBNP, GDF-15, TIMP-2, MMP-2, and hsTnI) were measured using immunoassays. Associations were assessed using logistic and linear regression, adjusting for demographics, substance use, and clinical characteristics. Among 381 participants with and without HIV, median age (IQR) was 55.1 (51.2, 58.4) years, 28% were female, 69% were Black, and 46% were current smokers. Sixty-two percent were PLWH (n = 235), of whom 88% were receiving cART and 72% were virally suppressed. PLWH had higher levels of sCD14 (p = 
ISSN:1471-2261
1471-2261
DOI:10.1186/s12872-022-02835-y