Cytokines and hs-CRP levels in individuals treated with low-dose aspirin a Cross Mark for cardiovascular prevention: A population-based study (CoLaus Study)

被引:23
作者
Vaucher, Julien [1 ,2 ]
Marques-Vidal, Pedro [2 ,3 ]
Waeber, Gerard [1 ,2 ]
Vollenweider, Peter [1 ,2 ]
机构
[1] CHU Vaudois, Dept Med, Lausanne, Switzerland
[2] Fac Biol & Med, Lausanne, Switzerland
[3] CHU Vaudois, Inst Social & Prevent Med IUMSP, Lausanne, Switzerland
基金
瑞士国家科学基金会;
关键词
Cytokines; hs-CRP; Low-dose aspirin; Cardiovascular prevention; Population-based sample; C-REACTIVE PROTEIN; CHRONIC STABLE ANGINA; INFLAMMATORY MARKERS; EUROPEAN-SOCIETY; TASK-FORCE; KAPPA-B; DISEASE; GUIDELINES; RISK; ATHEROSCLEROSIS;
D O I
10.1016/j.cyto.2014.01.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pro-inflammatory cytokines and high-sensitive C-reactive protein (hs-CRP) are associated with increased risk for cardiovascular disease. Low-dose aspirin for CV prevention is reported to have anti-inflammatory effects. The aim of this study was to determine the association between pro-inflammatory cytokines and hs-CRP levels and low-dose aspirin use for cardiovascular prevention in a population-based cohort (CoLaus Study). We assessed blood samples in 6085 participants (3201 women) aged 35-75 years. Medications' use and indications were recorded. Among aspirin users (n = 1'034; 17%), overall low-dose users (351; 5.8%) and low-dose for cardiovascular prevention users (324; 5.3%) were selected for analysis. Pro-inflammatory cytokines (IL-1 beta, IL-6 and TNF-alpha were assessed by a multiplex particle-based flow cytometric assay and hs-CRP by an immunometric assay. Cytokines and hs-CRP were presented in quartiles. Multivariate analysis adjusting for sex, age, smoking status, body mass index, diabetes mellitus and immunomodulatory drugs showed no association between cytokines and hs-CRP levels and low-dose aspirin use for cardiovascular prevention, either comparing the topmost vs. the three other quartiles (OR 95% CI, 0.84 (0.59-1.18), 1.03 (0.78-1.32), 1.10 (0.83-1.46), 1.00 (0.67-1.69) for IL-1 beta, IL-6, TNF-alpha and hs-CRP, respectively), or comparing the topmost quartile vs. the first one (OR 95% CI, 0.87 (0.60-1.26), 1.19 (0.79-1.79), 1.26 (0.86-1.84), 1.06 (0.67-1.69)). Low-dose aspirin use for cardiovascular prevention does not impact plasma pro-inflammatory cytokine and hs-CRP levels in a population-based cohort. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:95 / 100
页数:6
相关论文
共 44 条
[1]   Anti-inflammatory effects of aspirin and sodium salicylate [J].
Amann, R ;
Peskar, BA .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2002, 447 (01) :1-9
[2]  
Baigent C, 2002, BMJ-BRIT MED J, V324, P71, DOI 10.1136/bmj.324.7329.71
[3]   Circulating interleukin-1 beta, interleukin-6, tumor necrosis factor-alpha, and soluble ICAM-1 in patients with chronic stable angina and myocardial infarction [J].
Balbay, Y ;
Tikiz, H ;
Baptiste, RJ ;
Ayaz, S ;
Sasmaz, H ;
Korkmaz, S .
ANGIOLOGY, 2001, 52 (02) :109-114
[4]   Inflammatory cytokines impair endothelium-dependent dilatation in human veins in vivo [J].
Bhagat, K ;
Vallance, P .
CIRCULATION, 1997, 96 (09) :3042-3047
[5]   IKK/NF-κB and STAT3 pathways: central signalling hubs in inflammation-mediated tumour promotion and metastasis [J].
Bollrath, Julia ;
Greten, Florian R. .
EMBO REPORTS, 2009, 10 (12) :1314-1319
[6]  
Camm AJ, 2010, EUROPACE, V12, P1360, DOI [10.1093/europace/euq350, 10.1093/eurheartj/ehq278]
[7]   Effect of aspirin plus clopidogrel on inflammatory markers in patients with non-ST-segment elevation acute coronary syndrome [J].
Chen, YG ;
Xu, F ;
Zhang, Y ;
Ji, QS ;
Sun, Y ;
Lü, RJ ;
Li, RJ .
CHINESE MEDICAL JOURNAL, 2006, 119 (01) :32-36
[8]   STOP questionnaire - A tool to screen patients for obstructive sleep apnea [J].
Chung, Frances ;
Yegneswaran, Balaji ;
Liao, Pu ;
Chung, Sharon A. ;
Vairavanathan, Santhira ;
Islam, Sazzadul ;
Khajehdehi, Ali ;
Shapiro, Colin M. .
ANESTHESIOLOGY, 2008, 108 (05) :812-821
[9]   Local and systemic delivery of a stable aspirin-triggered lipoxin prevents neutrophil recruitment in vivo [J].
Clish, CB ;
O'Brien, JA ;
Gronert, K ;
Stahl, GL ;
Petasis, NA ;
Serhan, CN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (14) :8247-8252
[10]  
Collins R, 2009, LANCET, V373, P1849, DOI 10.1016/S0140-6736(09)60503-1