The prospective association of Chlamydia pneumoniae and four other pathogens with development of coronary artery calcium: The Multi-Ethnic Study of Atherosclerosis (MESA)

被引:13
|
作者
Laek, Babray [1 ,2 ]
Szklo, Moyses [1 ]
McClelland, Robyn L. [3 ]
Ding, Jingzhong [4 ]
Tsai, Michael Y. [5 ]
Bluemke, David A. [6 ]
Tracy, Russell [7 ]
Matsushita, Kunihiro [1 ]
机构
[1] Johns Hopkins Univ, Dept Epidemiol, Baltimore, MD 21205 USA
[2] Erasmus Univ, Netherlands Inst Hlth Sci, NL-3015 GJ Rotterdam, Netherlands
[3] Univ Washington, Dept Biostat, Seattle, WA 98115 USA
[4] Wake Forest Univ, Sch Med, Sticht Ctr Aging, Winston Salem, NC 27157 USA
[5] Univ Minnesota, Dept Lab Med & Pathol, Minneapolis, MN 55455 USA
[6] NIH, Bethesda, MD 20892 USA
[7] Univ Vermont, Dept Pathol, Colchester, VT 05446 USA
关键词
Coronary calcium; Atherosclerosis; Pathogens; Infection; AORTIC-STENOSIS; SUBCLINICAL ATHEROSCLEROSIS; CARDIOVASCULAR-DISEASE; RISK DEVELOPMENT; YOUNG-ADULTS; CALCIFICATION; PROGRESSION; ANTIBODIES; HEAT-SHOCK-PROTEIN-60; QUANTIFICATION;
D O I
10.1016/j.atherosclerosis.2013.07.053
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Previous basic and cross-sectional studies obtained conflicting results regarding the association of pathogens with coronary artery calcium (CAC). The aim of this study is to prospectively evaluate this association in a population-based cohort. Methods: We examined 5744 individuals aged 45-84 years at baseline (2000-02) who underwent repeated CAC assessment on average 2.4 years later (a half at visit 2 [2002-04] and the other half at visit 3 [2004-05]). CAC incidence was defined as newly detectable CAC at follow-up (475 cases of 2942 participants). CAC progression was defined as annualized change in CAC Agatston score >= 10 units/year if baseline CAC score >0 to <100 or >= 10%/year if baseline score >= 100 (1537 cases of 2802 participants). Seropositivity was assessed in the entire cohort for Chlamydia pneumoniae and in a random sample (n = 873) for Helicobacter pylori, cytomegalovirus, herpes simplex virus, and hepatitis A virus. Results: Seropositivity to C. pneumoniae was not significantly associated with CAC incidence (odds ratio [OR] 1.11 [95% CI, 0.88-1.39], P = 0.371) or progression (1.14 [0.96-1.36], P = 0.135) even in unadjusted models. When CAC incidence and progression were combined, we observed significant association with C. pneumoniae seropositivity before adjustment (OR 1.17 [1.03-1.33], P = 0.016) but not in a model adjusting for traditional risk factors (1.04 [0.90-1.19], P = 0.611). The results were consistent across subgroups according to age, sex, and race/ethnicity. None of five pathogens or their accrual was associated with CAC incidence and progression in the subsample. Conclusion: Our prospective study does not support the pathophysiological involvement of these pathogens in CAC development. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:268 / 274
页数:7
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