Plasma 8-iso-prostaglandin F2α , a marker of oxidative stress, is increased in patients with acute myocardial infarction

被引:42
|
作者
Elesber, AA
Best, PJ
Lennon, RJ
Mathew, V
Rihal, CS
Lerman, LO
Lerman, A
机构
[1] Mayo Clin & Mayo Fdn, Div Cardiovasc Med, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Div Biostat, Rochester, MN 55905 USA
[3] Mayo Clin & Mayo Fdn, Div Nephrol & Hypertens, Rochester, MN 55905 USA
关键词
oxidative stress; myocardial infarction; isoprostanes; artherosclerosis;
D O I
10.1080/10715760500539154
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Oxidative stress has been implicated in the pathogenesis of atherogenesis. The aim of our study is to examine whether the plasma 8-iso-prostaglandin F-2 alpha level, a marker of oxidative stress, is elevated in patients with acute myocardial infarction. Methods: Three groups of patients were enrolled: (1) patients with no or minimal coronary artery disease (CAD) (n = 15); (2) patients with stable CAD (n = 31); (3) patients with acute myocardial infarction (n = 13). Results: Plasma 8-iso-prostaglandin F-2 alpha levels were significantly elevated (p < 0.001) in patients with acute myocardial infarction (290.7 +/- 73.9 pg/ ml) as compared to patients with stable CAD (182.0 + 75.7 pg/ ml) and patients with no significant CAD (118.9 +/- 85.5 pg/ ml). This remained significant after correcting for coronary atherosclerosis risk factors, age, extent of atherosclerosis, and C-reactive protein (CRP) level. Conclusion: Plasma 8-iso-prostaglandin F-2 alpha levels are elevated in patients with acute myocardial infarction. Endogenous oxidative stress may contribute to the pathogenesis of atherosclerosis and its complications, namely myocardial infarction.
引用
收藏
页码:385 / 391
页数:7
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