Endothelial Progenitor Cells, Cardiovascular Risk Factors, Cytokine Levels and Atherosclerosis - Results from a Large Population-Based Study

被引:127
作者
Xiao, Qingzhong [1 ]
Kiechl, Stefan [2 ]
Patel, Seema [1 ]
Oberhollenzer, Friedrich [3 ]
Weger, Siegfried [2 ]
Mayr, Agnes [4 ]
Metzler, Bernhard [5 ]
Reindl, Markus [2 ]
Hu, Yanhua [1 ]
Willeit, Johann [2 ]
Xu, Qingbo [1 ]
机构
[1] Univ London, Kings Coll London, Div Cardiovasc, London, England
[2] Med Univ Innsbruck, Dept Neurol, Innsbruck, Austria
[3] Hosp Bruneck, Dept Internal Med, Brunico, Italy
[4] Hosp Bruneck, Dept Lab Med, Brunico, Italy
[5] Med Univ Innsbruck, Dept Internal Med, Innsbruck, Austria
来源
PLOS ONE | 2007年 / 2卷 / 10期
关键词
D O I
10.1371/journal.pone.0000975
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background. EPC number and functionality are assumed to reflect the endogenous vascular repair capacity with the EPC pool declining in higher ages and being exhausted by unfavorable life-style and risk factors. This intriguing and clinically highly relevant concept, however, has so far been derived from small case-control studies and patient series. Methodology and Principle Findings. In the population-based Bruneck Study EPC number and EPC-colony forming units (EPC-CFU) were assessed as part of the fourth follow-up evaluation (2005) in 571 and 542 subjects, respectively. EPC number declined with age (p = 0.013), was significantly lower in women (p = 0.006) and higher in subjects on statin, hormone replacement or ACE inhibitor/angiotensin-receptor blockers, and correlated positively with moderate alcohol consumption. Unexpectedly, a positive relation between EPC number and several vascular risk factors emerged. In a step forward multivariate linear regression analysis EPC number was independently related with SDF1 alpha, MMP-9, triglycerides, alcohol consumption, and Hba1c. EPC-CFU in turn was related to SDF1 alpha and diastolic blood pressure. Moreover, EPC number showed a significant positive association with the Framingham risk score (P = 0.001). Finally, there was an inverse association between EPC number and common carotid artery intima-media thickness (p = 0.02) and the carotid artery atherosclerosis score (p = 0.059). Conclusions. Our population-based data confirm the decline of EPC number with advancing age and lend first epidemiological support to a role of SDF-1 alpha and MMP9 in EPC differentiation, mobilization and homing, but are conflict with the view that EPC number is unfavorably affected by cardiovascular risk factors. EPC number increases with the cardiovascular risk estimated by the Framingham risk score (FRS), which in the absence of similar changes for EPC-CFU. Finally, we demonstrate a significant inverse association between EPC number and extent of carotid atherosclerosis even though this association was only of moderate strength and not entirely consistent in other vascular territories.
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