循环 T 细胞亚群与颈动脉僵化的关系:多种族动脉粥样硬化研究。

Theodore M DeConne, Petra Buzkova, Ryan Pewowaruk, Joseph AC Delaney, Bruce M. Psaty, Russell P. Tracy, Margaret F. Doyle, Colleen M Sitlani, Alan L. Landay, Sally Huber, Timothy M. Hughes, Alain G Bertoni, Adam D. Gepner, Nels C. Olson, Jingzhong Ding
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引用次数: 0

摘要

背景:以总脉搏波速度(T-PWV)测量的动脉僵化与多种老年相关疾病风险的增加有关。T-PWV可通过结构性(S-PWV)和负荷依赖性(LD-PWV)动脉僵化来描述。在人类和动物中,T 细胞与动脉重塑、血压和动脉僵化有关;但是,T 细胞是否与 S-PWV 或 LD-PWV 有关尚不清楚。因此,我们评估了外周 T 细胞亚群与 T-PWV、S-PWV 和 LD-PWV 硬度的横断面关联。研究方法在多族裔动脉粥样硬化研究(MESA,n=1,984)的一个子集中,使用流式细胞术对外周血 T 细胞进行表征,并使用 B 型超声波测量颈动脉,以计算基线检查时的 T-PWV。根据弹性模量和血压梯度,使用参与者特异性指数模型计算 S-PWV 和 LD-PWV。使用调整后的线性回归评估了五个主要免疫细胞亚群(p-significance<0.01)和二十五个探索性免疫细胞亚群(p-significance<0.05)每 1-SD 增量与动脉僵化测量值之间的关系。结果显示在主要分析中,CD4+CD28-CD57+ T细胞越多,调整共变量后,LD-PWV越高(?=0.04 m/s,p<0.01)。在探索性分析中,T 细胞亚群通常会随着年龄的增长而向记忆型和分化/免疫衰老型转变,在调整共变量后,这些亚群与更高的 T-PWV、S-PWV 和 LD-PWV 相关。结论:在这项横断面研究中,通常与衰老相关的几种 T 细胞亚群与动脉僵化的测量有关。有必要进行纵向研究,以检查 T 细胞亚群和动脉僵化指标的变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Associations of circulating T-cell subsets in carotid artery stiffness: the Multi-Ethnic Study of Atherosclerosis.
Background: Arterial stiffness measured by total pulse wave velocity (T-PWV) is associated with increased risk of multiple age-related diseases. T-PWV can be described by structural (S-PWV) and load-dependent (LD-PWV) arterial stiffening. T-cells have been associated with arterial remodeling, blood pressure, and arterial stiffness in humans and animals; however, it is unknown whether T-cells are related to S-PWV or LD-PWV. Therefore, we evaluated the cross-sectional associations of peripheral T-cell subpopulations with T-PWV, S-PWV, and LD-PWV stiffness. Methods: Peripheral blood T-cells were characterized using flow cytometry and the carotid artery was measured using B-mode ultrasound to calculate T-PWV at the baseline examination in a subset of the Multi-Ethnic Study of Atherosclerosis (MESA, n=1,984). A participant-specific exponential model was used to calculate S-PWV and LD-PWV based on elastic modulus and blood pressure gradients. The associations between five primary (p-significance<0.01) and twenty-five exploratory (p-significance<0.05) immune cell subpopulations, per 1-SD increment, and arterial stiffness measures were assessed using adjusted, linear regressions. Results: For the primary analysis, higher CD4+CD28-CD57+ T-cells were associated with higher LD-PWV (?=0.04 m/s, p<0.01) after adjusting for co-variates. For the exploratory analysis, T-cell subpopulations that commonly shift with aging towards memory and differentiated/immunosenescent phenotypes were associated with greater T-PWV, S-PWV, and LD-PWV after adjusting for co-variates. Conclusions: In this cross-sectional study, several T-cell subpopulations commonly associated with aging were related with measures of arterial stiffness. Longitudinal studies that examine changes in T-cell subpopulations and measures of arterial stiffness are warranted.
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