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Circulation. 2001;103:1071-1075

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(Circulation. 2001;103:1071.)
© 2001 American Heart Association, Inc.


Clinical Investigation and Reports

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

Evidence for an Autoimmune Component of Atherogenesis

Jianhui Zhu, MD, PhD; Arshed A. Quyyumi, MD; David Rott, MD; Gyorgy Csako, MD; Hongsheng Wu, PhD; Julian Halcox, MD; Stephen E. Epstein, MD

From the Cardiovascular Research Institute of the MedStar Research Institute, Washington Hospital Center, Washington, DC (J.Z., D.R., H.W., S.E.E.), and the National Heart, Lung, and Blood Institute and Clinical Center, National Institutes of Health, Bethesda, Md (A.A.Q., G.C., J.H.).

Correspondence to Dr Jianhui Zhu, Cardiovascular Research Institute, Washington Hospital Center, 110 Irving St, NW, Suite 4B-1, Washington, DC 20010.

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.


Key Words: coronary disease • proteins • immunology




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