PON1 QR192基因多态性及对氧磷酶、芳酰酯酶活性对深静脉血栓形成的影响

Hasim Akbalik, M. F. Polat, Ahmet Muderrisoglu, Z. Er, Ayşen Caniklioğlu, M. Ekim, H. Ekim
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Serum levels of triglyceride, total cholesterol, high-density lipoprotein-cholesterol, low-density lipoprotein-cholesterol, glucose, and c-reactive protein were measured by a similar method. Results There were no statistically significant differences between patients and controls regarding the frequency of variant allele for the PON1 QR192 polymorphism, activities of paraoxonase-arylesterase, and level of high-density lipoprotein-cholesterol. Triglyceride, total cholesterol, low-density lipoprotein-cholesterol, glucose, and c-reactive protein levels were significantly higher in patients compared to controls (p values were 0.005, 0.0002, 0.009, 0.0009, <0.0001, respectively.) Paraoxonase activity was found to be associated with PON1 QR192 genetic polymorphism (p<0.0001). 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引用次数: 0

摘要

摘要目的探讨PON1 QR192多态性(rs662)对深静脉血栓患者和健康人群甘油三酯、总胆固醇、高密度脂蛋白-胆固醇、低密度脂蛋白-胆固醇、葡萄糖和c反应蛋白水平以及对氧磷酶-芳酯酶活性的影响。方法选取45例深静脉血栓患者和45例正常人作为研究对象。采用聚合酶链反应和测序进行遗传分析。用分光光度计测定对氧磷酶和芳基酯酶活性。用类似方法测定血清甘油三酯、总胆固醇、高密度脂蛋白-胆固醇、低密度脂蛋白-胆固醇、葡萄糖和c反应蛋白水平。结果PON1 QR192多态性变异等位基因频率、对氧磷酶-芳烯酯酶活性、高密度脂蛋白-胆固醇水平与对照组比较,差异无统计学意义。与对照组相比,患者的甘油三酯、总胆固醇、低密度脂蛋白-胆固醇、葡萄糖和c反应蛋白水平显著升高(p值分别为0.005、0.0002、0.009、0.0009、<0.0001)。对氧磷酶活性与PON1 QR192基因多态性相关(p<0.0001)。然而,我们观察到PON1 QR192多态性与芳酰酯酶活性、甘油三酯、总胆固醇、高密度脂蛋白-胆固醇、低密度脂蛋白-胆固醇、葡萄糖和c反应蛋白水平没有关联。结论深静脉血栓患者与健康人群PON1 QR192基因多态性变异等位基因频率差异无统计学意义。此外,对氧磷酶和芳香酯酶活性在各组间相似。上述结果表明,PON1 QR192基因多态性和对氧磷酶芳酯酶活性水平对深静脉血栓形成无影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of PON1 QR192 genetic polymorphism and paraoxonase, arylesterase activities on deep vein thrombosis
Abstract Objectives We aimed to evaluate PON1 QR192 polymorphism’s (rs662) effects on levels of triglyceride, total cholesterol, high-density lipoprotein-cholesterol, low-density lipoprotein-cholesterol, glucose, and c-reactive protein, and paraoxonase-arylesterase activities among deep vein thrombosis patients and healthy subjects. Methods Forty-five deep vein thrombosis patients and 45 healthy subjects participated in the study. Genetic analysis was performed by using polymerase chain reaction and sequencing. Paraoxonase and arylesterase enzyme activities were determined by a spectrophotometer. Serum levels of triglyceride, total cholesterol, high-density lipoprotein-cholesterol, low-density lipoprotein-cholesterol, glucose, and c-reactive protein were measured by a similar method. Results There were no statistically significant differences between patients and controls regarding the frequency of variant allele for the PON1 QR192 polymorphism, activities of paraoxonase-arylesterase, and level of high-density lipoprotein-cholesterol. Triglyceride, total cholesterol, low-density lipoprotein-cholesterol, glucose, and c-reactive protein levels were significantly higher in patients compared to controls (p values were 0.005, 0.0002, 0.009, 0.0009, <0.0001, respectively.) Paraoxonase activity was found to be associated with PON1 QR192 genetic polymorphism (p<0.0001). However, we observed no association of PON1 QR192 polymorphism with arylesterase activity and, levels of triglyceride, total cholesterol, high-density lipoprotein-cholesterol, low-density lipoprotein-cholesterol, glucose, and c-reactive protein. Conclusions There was no statistically significant difference between deep vein thrombosis patients and healthy subjects regarding variant allele frequency for the PON1 QR192 genetic polymorphism. In addition, paraoxonase and arylesterase activities were similar among the groups. These results indicate that PON1 QR192 genetic polymorphism and activity levels of paraoxonase-arylesterase have no effect on the development of deep vein thrombosis.
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