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首页> 外文期刊>The American Journal of Clinical Nutrition: Official Journal of the American Society for Clinical Nutrition >Lipoprotein-associated phospholipase A2 activity is associated with coronary artery disease and markers of oxidative stress: a case-control study.
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Lipoprotein-associated phospholipase A2 activity is associated with coronary artery disease and markers of oxidative stress: a case-control study.

机译:脂蛋白相关的磷脂酶A2活性与冠心病和氧化应激标志物相关:一项病例对照研究。

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BACKGROUND: Lipoprotein-associated phospholipase A(2) (Lp-PLA(2)) is a lipoprotein-bound enzyme that can release atherogenic isoprostanes from esterified phospholipids and that may be involved in inflammation and atherosclerosis. OBJECTIVE: This study investigates the association between Lp-PLA(2) activity and coronary artery disease (CAD) in relation to oxidative stress markers, in particular urinary 8-epi-prostaglandin F(2alpha) (8-epi-PGF(2alpha)). DESIGN: We conducted a case-control study in which the cross-sectional relation between Lp-PLA(2) activity, lipoproteins, and oxidative stress markers was determined in 799 patients with angiographically confirmed CAD and 925 healthy controls. RESULTS: Lp-PLA(2) activity was significantly (P < 0.001) higher in CAD cases than in controls (32.9 +/- 0.46 and 29.7 +/- 0.42 nmol . mL(-1) . min(-1), respectively). Both elevated Lp-PLA(2) activity and urinary excretion concentrations of 8-epi-PGF(2alpha) were associated with greater CAD risk (P for trend < 0.001). Odds ratios for the upper quartiles of Lp-PLA(2) activity and 8-epi-PGF(2alpha).excretion were 2.47 (95% CI: 1.79, 3.40) and 2.19 (1.52, 3.15), respectively, after adjustment for sex, age, BMI, blood pressure, smoking and alcohol consumption status, and LDL and HDL cholesterol. When we examined the additive effect of both markers for CAD risk, the relation between 8-epi-PGF(2alpha) and CAD was weakened above the second quartile of Lp-PLA(2) activity. Moreover, Lp-PLA(2) activity was positively correlated with urinary excretion concentrations of 8-epi-PGF(2alpha) in controls (r = 0.277, P < 0.001) and cases (r = 0.202, P < 0.001) and with the tail moment of lymphocyte DNA (r = 0.213, P < 0.001) in controls. CONCLUSION: This study shows an association of elevated Lp-PLA(2) activity with CAD risk in relation to oxidant stress and thus supports a proatherogenic role of Lp-PLA(2).
机译:背景:脂蛋白相关的磷脂酶A(2)(Lp-PLA(2))是一种脂蛋白结合酶,可以从酯化的磷脂中释放出致动脉粥样硬化的异前列腺素,并可能参与炎症和动脉粥样硬化。目的:本研究调查了Lp-PLA(2)活性与冠状动脉疾病(CAD)的氧化应激标志物,特别是尿液中的8-epi-前列腺素F(2alpha)(8-epi-PGF(2alpha)之间的关系)。设计:我们进行了一项病例对照研究,在799例经血管造影证实的CAD患者和925例健康对照中,确定了Lp-PLA(2)活性,脂蛋白和氧化应激指标之间的横断面关系。结果:CAD患者的Lp-PLA(2)活性显着高于对照组(32.9 +/- 0.46和29.7 +/- 0.42 nmol。mL(-1)。min(-1)(P <0.001)。 )。升高的Lp-PLA(2)活性和8-epi-PGF(2alpha)的尿排泄浓度均与较高的CAD风险相关(趋势<0.001的P)。调整性别后,Lp-PLA(2)活动和8-epi-PGF(2alpha)排泄的最高四分位数的赔率分别是2.47(95%CI:1.79,3.40)和2.19(1.52,3.15) ,年龄,BMI,血压,吸烟和饮酒状况以及LDL和HDL胆固醇。当我们检查两种标记物对CAD风险的累加作用时,在Lp-PLA(2)活性的第二个四分位数以上,8-epi-PGF(2alpha)和CAD之间的关系被削弱。此外,Lp-PLA(2)活性与对照组(r = 0.277,P <0.001)和病例(r = 0.202,P <0.001)和尿液中8-epi-PGF(2alpha)的尿排泄浓度呈正相关。对照中淋巴细胞DNA的尾矩(r = 0.213,P <0.001)。结论:这项研究表明,Lp-PLA(2)活性升高与氧化应激相关的CAD风险相关,因此支持Lp-PLA(2)的促动脉粥样硬化作用。

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