High oxidative stress in patients with stable coronary heart disease

被引:117
作者
Weinbrenner, T
Cladellas, M
Covas, MI
Fitó, M
Tomás, M
Sentí, M
Bruguera, J
Marrugat, J
机构
[1] Inst Invest Med, Unitat Lipids & Epidemiol Cardiovasc, E-08003 Barcelona, Spain
[2] Hosp Mar, Serv Cardiol, Barcelona, Spain
[3] Lab Referencia Catalunya, Barcelona, Spain
[4] Univ Pompeu Fabra, Barcelona, Spain
[5] Univ Autonoma Barcelona, E-08193 Barcelona, Spain
关键词
stable coronary heart disease; oxidized LDL; antibodies against oxidized LDL; superoxide dismutase; glutathione peroxidase; paraoxonasel activity; oxidative stress;
D O I
10.1016/S0021-9150(03)00053-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Oxidized low density lipoprotein (oxLDL) plays a pivotal role in the development of atherosclerosis. The aim of the study was to investigate the relationship between oxLDL and other oxidative stress biomarkers with stable coronary heart disease (CHD). We compared the degree of oxidative stress in patients with CHD and sex-matched healthy control subjects in a case-control study. The study included 64 male subjects: 32 patients with stable CHD and 32 normal control subjects. Levels of circulating oxLDL were measured by a monoclonal antibody 4E6-based competition ELISA. Comparison of oxidative stress marker levels between cases and controls, adjusted for age, revealed significantly higher plasma oxLDL levels (63.32 +/- 25.49 vs. 37.73 +/- 20.58 U/l, P = 0.001), lower serum levels of autoantibodies against oxLDL (341.53 +/- 350.46 vs. 796.45 +/- 1034.2 mU/ml, P = 0.021), higher activities of the antioxidant enzymes superoxide dismutase in erythrocytes (951 +/- 70.2 vs. 771.6 +/- 191.2 U/g, P = 0.032) and glutathione peroxidase in whole blood (GSH-Px: 10714.4 +/- 3705.4 vs. 5512.2 +/- 1498.1 U/l, P < 0.001). The risk of having CHD was 20.6-fold greater (95% Cl, 1.86-228.44, P = 0.014) in the highest tertile of the oxLDL distribution than in the lowest, determined by logistic regression analysis on the combined study population after adjustment for age and other potential confounding factors. When the risk associated with GSH-Px levels was calculated, the odds ratio was 305.3 (95% CI, 5.07-18369.95, P = 0.006) in the highest tertile compared with the lowest. Our results showed that an oxidative stress occurs in patients with CHD despite being clinically stable and under medical treatment. The combination of oxLDL levels and GSH-Px activity may be useful for the identification of patients with stable CHD. (C) 2003 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:99 / 106
页数:8
相关论文
共 34 条
[11]   Antibody titers against oxidized LDL are not elevated in patients with familial hypercholesterolemia [J].
Hulthe, J ;
Wikstrand, J ;
Lidell, A ;
Wendelhag, I ;
Hansson, GK ;
Wiklund, O .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1998, 18 (08) :1203-1211
[12]   Antibodies to oxidized LDL in relation to carotid atherosclerosis, cell adhesion molecules, and phospholipase A2 [J].
Hulthe, J ;
Wiklund, O ;
Hurt-Camejo, E ;
Bondjers, G .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2001, 21 (02) :269-274
[13]   Autoantibodies against oxidized low density lipoprotein in patients with angiographically verified coronary artery disease [J].
Lehtimäki, T ;
Lehtinen, S ;
Solakivi, T ;
Nikkilä, M ;
Jaakkola, O ;
Jokela, H ;
Ylä-Herttuala, S ;
Luoma, JS ;
Koivula, T ;
Nikkari, T .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1999, 19 (01) :23-27
[14]   Antibodies to oxidized LDL and LDL-containing immune complexes as risk factors for coronary artery disease in diabetes mellitus [J].
Lopes-Virella, MF ;
Virella, G ;
Orchard, TJ ;
Koskinen, S ;
Evans, RW ;
Becker, DJ ;
Forrest, KYZ .
CLINICAL IMMUNOLOGY, 1999, 90 (02) :165-172
[15]  
MCCORD JM, 1969, J BIOL CHEM, V244, P6049
[16]  
PAGLIA DE, 1967, J LAB CLIN MED, V70, P158
[17]   IMMUNIZATION OF LOW-DENSITY-LIPOPROTEIN (LDL) RECEPTOR-DEFICIENT RABBITS WITH HOMOLOGOUS MALONDIALDEHYDE-MODIFIED LDL REDUCES ATHEROGENESIS [J].
PALINSKI, W ;
MILLER, E ;
WITZTUM, JL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (03) :821-825
[18]   ANTIBODY AGAINST OXIDIZED LOW-DENSITY-LIPOPROTEIN PREDICTING MYOCARDIAL-INFARCTION [J].
PUURUNEN, M ;
MANTTARI, M ;
MANNINEN, V ;
TENKANEN, L ;
ALFTHAN, G ;
EHNHOLM, C ;
VAARALA, O ;
AHO, K ;
PALOSUO, T .
ARCHIVES OF INTERNAL MEDICINE, 1994, 154 (22) :2605-2609
[19]   PARTICLE-SIZE - THE KEY TO THE ATHEROGENIC LIPOPROTEIN [J].
RAJMAN, I ;
MAXWELL, S ;
CRAMB, R ;
KENDALL, M .
QUARTERLY JOURNAL OF MEDICINE, 1994, 87 (12) :709-720
[20]   SUSCEPTIBILITY TO LOW-DENSITY-LIPOPROTEIN OXIDATION AND CORONARY ATHEROSCLEROSIS IN MAN [J].
REGNSTROM, J ;
NILSSON, J ;
TORNVALL, P ;
LANDOU, C ;
HAMSTEN, A .
LANCET, 1992, 339 (8803) :1183-1186