循环CD34+细胞计数与无症状阿米什男性亚临床动脉粥样硬化程度相关,独立于10年Framingham风险

Lawrence F Bielak, Richard B Horenstein, Kathleen A Ryan, Patrick F Sheedy, John A Rumberger, Keith Tanner, Wendy Post, Braxton D Mitchell, Alan R Shuldiner, Patricia A Peyser
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引用次数: 27

摘要

背景:骨髓源性祖细胞(PCs)可能通过主动修复受损内皮在维持血管健康中发挥作用。本研究在无高血压或糖尿病的无症状Old Order Amish男性(n = 90)中进行,目的是确定PC计数(由外周血CD34+细胞计数测定)是否与10年心血管疾病(CVD)风险和亚临床动脉粥样硬化指标相关。方法和结果:采用荧光活化细胞分选法获得CD34+细胞计数,采用电子束计算机断层扫描获得冠状动脉钙化(CAC)情况,并分析心血管疾病的危险因素。在57名男性中也获得了颈动脉内膜-内侧厚度(CIMT)。在调整10年心血管疾病风险后,CD34+细胞计数与CAC数量(p = 0.03)和CIMT (p < 0.0001)显著相关。自然对数转化CD34+细胞计数每增加1个单位,CAC数量减少55.2% (95% CI: -77.8%至-9.3%),CIMT减少14.3% (95% CI: -20.1%至-8.1%)。结论:CD34+细胞计数的增加与多动脉床亚临床动脉粥样硬化程度的降低有关,与10年CVD风险无关。进一步研究无症状个体中CD34+细胞计数与亚临床动脉粥样硬化的关系,可以为动脉粥样硬化过程提供机制见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Circulating CD34+ Cell Count is Associated with Extent of Subclinical Atherosclerosis in Asymptomatic Amish Men, Independent of 10-Year Framingham Risk.

Background: Bone-marrow derived progenitor cells (PCs) may play a role in maintaining vascular health by actively repairing damaged endothelium. The purpose of this study in asymptomatic Old Order Amish men (n = 90) without hypertension or diabetes was to determine if PC count, as determined by CD34+ cell count in peripheral blood, was associated with 10-year risk of cardiovascular disease (CVD) and measures of subclinical atherosclerosis.

Methods and results: CD34+ cell count by fluorescence-activated cell sorting, coronary artery calcification (CAC) by electron beam computed tomography, and CVD risk factors were obtained. Carotid intimal-medial thickness (CIMT) also was obtained in a subset of 57 men. After adjusting for 10-year CVD risk, CD34+ cell count was significantly associated with CAC quantity (p = 0.03) and CIMT (p < 0.0001). A 1-unit increase in natural-log transformed CD34+ cell count was associated with an estimated 55.2% decrease (95% CI: -77.8% to -9.3%) in CAC quantity and an estimated 14.3% decrease (95% CI: -20.1% to -8.1%) in CIMT.

Conclusions: Increased CD34+ cell count was associated with a decrease in extent of subclinical atherosclerosis in multiple arterial beds, independent of 10-year CVD risk. Further investigations of associations of CD34+ cell count with subclinical atherosclerosis in asymptomatic individuals could provide mechanistic insights into the atherosclerotic process.

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