氧化低密度脂蛋白和髓过氧化物酶在心血管疾病筛查中的意义和准确性的实验和验证

D. Mandsorwale, B. Sharma
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引用次数: 0

摘要

的目标。为了获得髓过氧化物酶和氧化低密度脂蛋白相互之间的优势,作为获得心血管疾病严重程度信息的更好的预测标志物。材料和方法。共纳入215例受试者,其中健康对照54例,稳定型心绞痛52例,不稳定型心绞痛53例,急性心肌梗死56例。脂质参数、氧化应激标志物、血浆髓过氧化物酶和血浆氧化低密度脂蛋白分别采用试剂盒法、硫代巴比妥酸反应物质法、比色法、三明治法和竞争性酶联免疫吸附法测定。结果以mean±SD表示,p值<0.05为显著性,采用Student 's unpaired“t”检验。通过盒须图进行对比分析,以检查值内的偏度和偏差。采用SPSS 17.0软件进行数据分析。结果。氧化低密度脂蛋白水平在所有三个病例亚组中均显著升高,而与对照组相比,稳定型心绞痛患者髓过氧化物酶水平不显著。在稳定性心绞痛和急性心肌梗死中,髓过氧化物酶水平的箱形图和须子图显示无偏态(不显著),而不稳定心绞痛和急性心肌梗死显示右偏态(高度显著),而氧化低密度脂蛋白的图在稳定心绞痛亚组中显示广泛的四分位数范围,表明与不稳定心绞痛和急性心肌梗死亚组相比,平均值存在分散偏差。结论。研究得出结论,稳定型心绞痛、不稳定型心绞痛和急性心肌梗死亚组中氧化低密度脂蛋白水平显著升高,稳定型心绞痛亚组中氧化低密度脂蛋白水平有分散偏差,反映了其与血浆髓过氧化物酶的预后可靠性较低,稳定型心绞痛亚组中氧化低密度脂蛋白水平有轻微偏差,稳定型心绞痛亚组中氧化低密度脂蛋白水平升高不显著。因此,血浆髓过氧化物酶和氧化低密度脂蛋白水平可作为心血管疾病的独立预测指标,但血浆髓过氧化物酶水平可预测稳定型和不稳定型心绞痛患者随后心血管事件中氧化低密度脂蛋白水平升高的风险,并扩展了从传统生化标志物获得的预后信息
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Experimental and validation of significance and accuracy of oxidized low-density lipoproteins and myeloperoxidase in the screening of cardio-vascular disease
The aim. To access the superiority of myeloperoxidase & oxidized low-density lipoproteins over each other acts as a better predictive marker gaining information regarding the severity of cardiovascular disease. Materials and methods. 215 subjects are taken into consideration of which 54 are healthy controls, 52 are from stable angina pectoris, 53 are taken from unstable angina pectoris and 56 subjects are from acute myocardial infarction. Lipid profile parameters, oxidative stress markers, plasma myeloperoxidase and plasma oxidized low density lipoproteins were estimated by kit methods, thiobarbituric acid reactive substances method, and colorimetric assay, sandwich and competitive enzyme linked immunosorbent assay techniques, respectively. Results were present as mean ± SD, p-values <0.05 as significant, and Student’s unpaired “t” test. Comparative analysis by box and whiskers plot to check skewness and deviations within the values. Data analysis was performed by software package SPSS version 17.0. Results. The oxidized low density lipoproteins levels found significantly elevated in all three cases subgroup contrary to insignificant levels of myeloperoxidase in stable angina pectoris compared to control. Box and whisker plot of myeloperoxidase levels showed no skewness in stable angina pectoris (non-significant), whereas unstable angina pectoris and acute myocardial infarction showed right skewness (highly significant), whereas plots of oxidized low-density lipoproteins show extensive interquartile range in the stable angina pectoris subgroup, suggesting scattered deviation in the mean values compared to unstable angina pectoris and acute myocardial infarction subgroup. Conclusions. The study concluded that significantly elevated level of oxidized low-density lipoproteins in stable angina pectoris, unstable angina pectoris, and acute myocardial infarction subgroups with a scattered deviation of oxidized low density lipoproteins levels in the stable angina pectoris subgroup reflects its low prognostic reliability compared to plasma myeloperoxidase with marginal deviation and in insignificant elevation in stable angina pectoris. Thus, plasma myeloperoxidase and oxidized low density lipoproteins levels serve as independent predictors of cardiovascular disease, but plasma myeloperoxidase levels predict an increased risk over oxidized low density lipoproteins for subsequent cardiovascular events in stable and unstable angina and extend the prognostic information gained from traditional biochemical markers
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