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Antibodies to Human Heat-Shock Protein 60 Are Associated With the Presence and Severity of Coronary Artery Disease

Authors :
Hongsheng Wu
David Rott
Julian Halcox
Gyorgy Csako
Jianhui Zhu
Stephen E. Epstein
Arshed A. Quyyumi
Source :
Scopus-Elsevier
Publication Year :
2001
Publisher :
Ovid Technologies (Wolters Kluwer Health), 2001.

Abstract

Background —Antibodies to mycobacterial heat-shock protein (HSP) 65 have been reported to be associated with carotid artery thickening. We examined whether antibodies to human HSP60 are associated with the risk of coronary artery disease (CAD). Methods and Results —Blood samples from 391 patients (62% men, mean age 57 years) being evaluated for CAD by coronary angiography were tested for IgG antibodies to human HSP60 by ELISA. We found that 75% of the study subjects had anti-HSP60 antibodies. The prevalence of CAD was increased in seropositive compared with seronegative patients (68% versus 49%, P =0.0009). Mean titers of HSP60 antibodies were higher in CAD patients than in non-CAD patients ( P =0.008). No association between HSP60 antibodies and infection or inflammation was found. Importantly, HSP60 antibodies were related to disease severity. The prevalence of HSP60 antibodies was 76%, 80%, and 85% in patients with 1-, 2-, and 3-vessel disease, compared with 64% in patients without CAD ( P for trend=0.003). A similar association between increasing antibody titers and number of diseased vessels was also found ( P =0.03). Significant associations between antibodies to HSP60 and CAD severity persisted after adjustment for traditional risk factors by age, race, sex, smoking, diabetes, hypercholesterolemia, hypertension, and C-reactive protein levels. Adjusted OR for number of vessels diseased was 1.86 (95% CI 1.13 to 3.04). Conclusions —This is the first study demonstrating a significant association between human HSP60 antibodies and both the presence and severity of CAD.

Details

ISSN :
15244539 and 00097322
Volume :
103
Database :
OpenAIRE
Journal :
Circulation
Accession number :
edsair.doi.dedup.....6e03fb9d378143c0c91b5bfe176935d6
Full Text :
https://doi.org/10.1161/01.cir.103.8.1071