Decreased Circulating Endothelial Progenitor Cell Levels and Function in Patients with Nonalcoholic Fatty Liver Disease

被引:46
|
作者
Chiang, Chia-Hung [1 ,5 ]
Huang, Po-Hsun [1 ,4 ,5 ]
Chung, Fa-Po [1 ,5 ]
Chen, Zu-Yin [1 ,5 ]
Leu, Hsin-Bang [1 ,3 ,4 ,5 ]
Huang, Chin-Chou [1 ,2 ,5 ,6 ]
Wu, Tao-Cheng [1 ,4 ,5 ]
Chen, Jaw-Wen [1 ,2 ,5 ,6 ]
Lin, Shing-Jong [1 ,2 ,4 ,5 ]
机构
[1] Taipei Vet Gen Hosp, Div Cardiol, Taipei, Taiwan
[2] Taipei Vet Gen Hosp, Dept Med Res & Educ, Taipei, Taiwan
[3] Taipei Vet Gen Hosp, Healthcare & Management Ctr, Taipei, Taiwan
[4] Natl Yang Ming Univ, Inst Clin Med, Taipei 112, Taiwan
[5] Natl Yang Ming Univ, Cardiovasc Res Ctr, Taipei 112, Taiwan
[6] Natl Yang Ming Univ, Inst & Dept Pharmacol, Taipei 112, Taiwan
来源
PLOS ONE | 2012年 / 7卷 / 02期
关键词
CORONARY-ARTERY-DISEASE; C-REACTIVE PROTEIN; INCREASED CARDIOVASCULAR RISK; METABOLIC SYNDROME; GENERAL-POPULATION; INSULIN-RESISTANCE; PERIPHERAL-BLOOD; DYSFUNCTION; ATHEROSCLEROSIS; PREVALENCE;
D O I
10.1371/journal.pone.0031799
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
Objectives: Nonalcoholic fatty liver disease (NAFLD) is associated with advanced atherosclerosis and a higher risk of cardiovascular disease. Increasing evidence suggests that injured endothelial monolayer is regenerated by circulating bone marrow derived-endothelial progenitor cells (EPCs), and levels of circulating EPCs reflect vascular repair capacity. However, the relation between NAFLD and EPC remains unclear. Here, we tested the hypothesis that patients with nonalcoholic fatty liver disease (NAFLD) might have decreased endothelial progenitor cell (EPC) levels and attenuated EPC function. Methods and Results: A total of 312 consecutive patients undergoing elective coronary angiography because of suspected coronary artery disease were screened and received examinations of abdominal ultrasonography between July 2009 and November 2010. Finally, 34 patients with an ultrasonographic diagnosis of NAFLD, and 68 age-and sex-matched controls without NAFLD were enrolled. Flow cytometry with quantification of EPC markers (defined as CD34(+), CD34(+)KDR(+), and CD34(+)KDR(+)CD133(+))in peripheral blood samples was used to assess circulating EPC numbers. The adhesive function, and migration, and tube formation capacities of EPCs were also determined in NAFLD patients and controls. Patients with NAFLD had a significantly higher incidence of metabolic syndrome, previous myocardial infarction, hyperuricemia, and higher waist circumference, body mass index, fasting glucose and triglyceride levels. In addition, patients with NAFLD had significantly decreased circulating EPC levels (all P<0.05), attenuated EPC functions, and enhanced systemic inflammation compared to controls. Multivariate logistic regression analysis showed that circulating EPC level (CD34(+)KDR(+) [cells/10(5) events]) was an independent reverse predictor of NAFLD (Odds ratio: 0.78; 95% confidence interval: 0.69-0.89, P<0.001). Conclusions: NAFLD patients have decreased circulating EPC numbers and functions than those without NAFLD, which may be one of the mechanisms to explain atherosclerotic disease progression and enhanced cardiovascular risk in patients with NAFLD.
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页数:9
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