Anti-heat shock protein-27 (Hsp-27) antibody levels in patients with chest pain: Association with established cardiovascular risk factors

被引:30
作者
Shams, Sedigheh [3 ]
Shafi, Shahida [1 ]
Bodman-Smith, Kikki
Williams, Peter [4 ]
Mehta, Sweta [2 ]
Ferns, Gordon A. [2 ]
机构
[1] Univ Surrey, Fac Hlth & Med Sci, Div Biochem Sci, Surrey GU2 7XH, England
[2] Royal Surrey Cty Hosp, Surrey, England
[3] Univ Tehran, Childrens Med Ctr, Dept Med Sci, Tehran 14174, Iran
[4] Univ Surrey, Fac Engn & Phys Sci, Surrey GU2 7XH, England
关键词
heat shock protein-27; acute myocardial infarction; IgG antibody levels; ELISA;
D O I
10.1016/j.cca.2008.04.026
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Antibody titres to several heat shock proteins (Hsps) have been shown to be associated with risk factors for cardiovascular disease (CVD), but there are no data for Hsp-27. We developed an ELISA for total IgG antibody concentrations, applying this to individuals with and without acute coronary syndrome, and have assessed the relationship between antibody levels and individual coronary risk factors. Methods: Blood was collected from 63 healthy controls without a history of chest pain or CVD and 60 patients admitted to hospital with acute cardiac chest pain on admission and approximately 12 h after the acute event. Results: Patients with chest pain had significantly higher Hsp-27 antibody levels than controls [median 0.16 (range 0.01-0.51) vs. 0.10 (range 0.00-0.32); p<0.001]. Furthermore, Hsp-27 antibody concentrations showed strong associations with age and hypertension (Standardised beta coefficient = 0.343, p<0.001 and = -0.235, p<0.016, respectively), but not with other established cardiovascular risk factors. Logistic regression analysis showed age and diabetes were significant predictors of risk of CVD with OR 1.29 (95% CI 1.16 to 1.42, p=0.001) and 25.9 (95% CI 2.14>312, p=0.01) respectively. Conclusions: Raised antibody levels to Hsp-27 were associated only with age and hypertension. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:42 / 46
页数:5
相关论文
共 30 条
[21]   Autoantibodies against heat shock protein 60 mediate endothelial cytotoxicity [J].
Schett, G ;
Xu, QB ;
Amberger, A ;
VanderZee, R ;
Recheis, H ;
Willeit, J ;
Wick, G .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 96 (06) :2569-2577
[22]   Dual perinatal and developmental expression of the small heat shock proteins αB-crystallin and Hsp27 in different tissues of the developing piglet [J].
Tallot, P ;
Grongnet, JF ;
David, JC .
BIOLOGY OF THE NEONATE, 2003, 83 (04) :281-288
[23]  
Vaidya N, 2005, CLIN CHIM ACTA, V355, pS118
[24]   Increased expression of HSP27 protects canine myocytes from simulated ischemia-reperfusion injury [J].
Vander Heide, RS .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2002, 282 (03) :H935-H941
[25]   Atherosclerosis - An autoimmune disease due to an immune reaction against heat-shock protein 60 [J].
Wick, G .
HERZ, 2000, 25 (02) :87-90
[26]   Serum soluble heat shock protein 60 is elevated in subjects with atherosclerosis in a general population [J].
Xu, QB ;
Schett, G ;
Perschinka, H ;
Mayr, M ;
Egger, G ;
Oberhollenzer, F ;
Willeit, J ;
Kiechl, S ;
Wick, G .
CIRCULATION, 2000, 102 (01) :14-20
[27]   Role of heat shock proteins in atherosclerosis [J].
Xu, QB .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2002, 22 (10) :1547-1559
[28]   Association of serum antibodies to heat-shock protein 65 with carotid atherosclerosis - Clinical significance determined in a follow-up study [J].
Xu, QB ;
Kiechl, S ;
Mayr, M ;
Metzler, B ;
Egger, G ;
Oberhollenzer, F ;
Willeit, J ;
Wick, G .
CIRCULATION, 1999, 100 (11) :1169-1174
[29]   Evidence for modulation of smooth muscle force by the p38 MAP kinase/HSP27 pathway [J].
Yamboliev, IA ;
Hedges, JC ;
Mutnick, JLM ;
Adam, LP ;
Gerthoffer, WT .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2000, 278 (06) :H1899-H1907
[30]   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 [J].
Zhu, JH ;
Quyyumi, AA ;
Rott, D ;
Csako, G ;
Wu, HS ;
Halcox, J ;
Epstein, SE .
CIRCULATION, 2001, 103 (08) :1071-1075