Levels of zinc and lipid peroxidation in acute coronary syndrome

被引:19
作者
Cikim, G
Canatan, H
Gursu, MF [1 ]
Gulcu, F
Baydas, G
Kilicoglu, AE
机构
[1] Firat Univ, Coll Med, Dept Biochem, Elazig, Turkey
[2] Mustafa Kemal Univ, Dept Biochem, Hatay, Turkey
[3] Mustafa Kemal Univ, Dept Cardiol, Coll Med, Hatay, Turkey
[4] Firat Univ, Coll Med, Dept Med Biol, Elazig, Turkey
[5] Firat Univ, Coll Med, Dept Physiol, Elazig, Turkey
关键词
acute coronary syndrome; lipid peroxidation; MDA; zinc;
D O I
10.1385/BTER:96:1-3:61
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The present study was carried out on 20 female patients diagnosed with acute coronary syndrome (ACS). The control group was composed of 20 healthy female volunteers. Plasma malondialdehyde (MDA) levels and serum zinc (Zn), total cholesterol, low-density lipoprotein (LDL) cholesterol, high-density lipoprotein (HDL) cholesterol, and VLDL-cholesterol, Lp(a), Apo-A(1), and Apo-B were determined in all patients and controls. Plasma MDA levels were determined to be significantly high in patients with ACS compared to the controls (1.75+/-0.27 vs 0.8+/-0.43 nmol/mL; p<0.05). On the other hand, Zn levels in patients with ACS were determined to be significantly low compared to the control group (67.9+/-14.8 vs 101.8+/-22.4 mg/dL; p<0.05). There was a statistically significant negative correlation between MDA and Zn levels in patients with ACS (r = -0.678, p<0.05). Other lipid parameters were significantly altered in patients with ACS compared to the controls (p<0.05). In conclusion, Zn and lipid peroxidation levels are important in patients with ACS and they must be monitored during diagnosis and treatment of these patients.
引用
收藏
页码:61 / 69
页数:9
相关论文
共 27 条
[1]
Daily rhythm of glutathione peroxidase activity, lipid peroxidation and glutathione levels in tissues of pinealectomized rats [J].
Baydas, G ;
Gursu, MF ;
Yilmaz, S ;
Canpolat, S ;
Yasar, A ;
Cikim, G ;
Canatan, H .
NEUROSCIENCE LETTERS, 2002, 323 (03) :195-198
[2]
The role of Fas/APO 1 and apoptosis in the development of human atherosclerotic lesions [J].
Cai, WJ ;
Devaux, B ;
Schaper, W ;
Schaper, J .
ATHEROSCLEROSIS, 1997, 131 (02) :177-186
[3]
CIKIM G, 2002, THESIS FIRAT U ELAZI
[4]
CLAIR J, 1995, J TRACE ELEM EXP MED, V7, P143
[5]
DAVIES M, 1990, CIRCULATION S3, V82, P1138
[6]
DAVIES MJ, 1997, CLIN CARDIOL, V20, P12
[7]
LIPID-PEROXIDATION AND ITS ROLE IN ATHEROSCLEROSIS [J].
ESTERBAUER, H ;
WAG, G ;
PUHL, H .
BRITISH MEDICAL BULLETIN, 1993, 49 (03) :566-576
[8]
MECHANISMS OF DISEASE - THE PATHOGENESIS OF CORONARY-ARTERY DISEASE AND THE ACUTE CORONARY SYNDROMES .1. [J].
FUSTER, V ;
BADIMON, L ;
BADIMON, JJ ;
CHESEBRO, JH .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 326 (04) :242-250
[9]
TYPE-II DIABETES-MELLITUS, CONGESTIVE-HEART-FAILURE, AND ZINC-METABOLISM [J].
GOLIK, A ;
COHEN, N ;
RAMOT, Y ;
MAOR, J ;
MOSES, R ;
WEISSGARTEN, J ;
LEONOV, Y ;
MODAI, D .
BIOLOGICAL TRACE ELEMENT RESEARCH, 1993, 39 (2-3) :171-175
[10]
Longitudinal study of serum copper and zinc levels and their distribution in blood proteins after acute myocardial infarction [J].
Gomez, E ;
del Diego, C ;
Orden, I ;
Elósegui, LM ;
Borque, L ;
Escanero, JF .
JOURNAL OF TRACE ELEMENTS IN MEDICINE AND BIOLOGY, 2000, 14 (02) :65-70