Assessment of arterial elasticity among HIV-positive participants with high CD4 cell counts: a substudy of the INSIGHT Strategic Timing of AntiRetroviral Treatment (START) trial

被引:11
作者
Baker, J. V. [1 ,2 ]
Engen, N. W. [2 ]
Hullsiek, K. Huppler [2 ]
Stephan, C. [3 ]
Jain, M. K. [4 ]
Munderi, P. [5 ]
Pett, S. [6 ]
Duprez, D. [2 ]
机构
[1] Univ Minnesota, Hennepin Cty Med Ctr, Minneapolis, MN 55415 USA
[2] Univ Minnesota, Minneapolis, MN USA
[3] Goethe Univ Hosp Frankfurt, Frankfurt, Germany
[4] Parkland Hlth & Hosp Syst, UT Southwestern Med Ctr, Dallas, TX USA
[5] Uganda Virus Res Inst, Entebbe, Uganda
[6] UCL, London, England
基金
英国医学研究理事会; 美国国家卫生研究院;
关键词
arterial elasticity; cardiovascular disease; HIV infection; vascular dysfunction; PULSE-WAVE VELOCITY; ALL-CAUSE MORTALITY; C-REACTIVE PROTEIN; CARDIOVASCULAR-DISEASE; ENDOTHELIAL FUNCTION; ASSOCIATION; INFECTION; RISK; ATHEROSCLEROSIS; STIFFNESS;
D O I
10.1111/hiv.12239
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
ObjectivesBoth HIV infection and antiretroviral therapy (ART) may increase cardiovascular disease (CVD) risk. Assessments of vascular function and structure can be used to study the pathogenesis and progression of CVD, including the effects of ART and other interventions. The objective of this report is to understand methods to assess vascular (dys)function and report our experience in the Arterial Elasticity Substudy in the Strategic Timing of AntiRetroviral Treatment (START) trial. MethodsWe review literature and analyze baseline data from the Arterial Elasticity Substudy, which estimated vascular (dys)function through analysis of the diastolic blood pressure (BP) waveform. Linear regression was used to study cross-sectional associations between baseline clinical factors and small or large arterial elasticity. ResultsArterial elasticity measurement was chosen for its improved measurement reproducibility over other methodologies and the potential of small arterial elasticity to predict clinical risk. Analysis of baseline data demonstrates that small artery elasticity is impaired (lower) with older age and differs by race and between geographical regions. No HIV-specific factors studied remained significantly associated with arterial elasticity in multivariate models. ConclusionsLongitudinal analyses in this substudy will provide essential randomized data with which to study the effects of early ART initiation on the progression of vascular disease among a diverse global population. When combined with future biomarker analyses and clinical outcomes in START, these findings will expand our understanding of the pathogenesis of HIV-related CVD.
引用
收藏
页码:109 / 118
页数:10
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