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对氧磷酶 1(PON1)多态性与偏头痛风险。

Paraoxonase 1 (PON1) polymorphisms and risk for migraine.

机构信息

Department of Biochemistry and Molecular Biology, School of Biological Sciences, University of Extremadura, Badajoz, Spain.

出版信息

J Neurol. 2010 Sep;257(9):1482-5. doi: 10.1007/s00415-010-5551-2. Epub 2010 Apr 21.

Abstract

The polymorphic enzyme human serum paraoxonase 1 (PON1), encoded by the gene PON1 (chromosome 7q21.3) plays a role as an antioxidant molecule through several mechanisms. Because oxidative stress has been implicated in the pathogenesis of migraine, we have investigated the possible association between the nonsynonymous polymorphisms 55LM and 192QR in the PON1 and the risk for migraine. We studied the frequency of the PON1 genotypes and allelic variants in 197 patients with migraine and 220 healthy controls using a TaqMan single nucleotide polymorphism analysis. The frequencies of the PON1 genotypes and PON1 allelic variants did not differ significantly between patients with migraine and controls, and were unrelated with gender, family history of migraine, and presence or absence of aura. The frequencies of the genotype PON1 192QQ and the allelic variant PON1 192Q were significantly higher in patients with earlier onset of migraine. The results of the present study suggest that PON1 polymorphisms are not related with the risk for migraine in Caucasian Spanish people, although PON1 192Q/Q genotype and PON1 192Q allelic variant should be related with an earlier onset of migraine.

摘要

人血清对氧磷酶 1(PON1)是一种多态酶,由 PON1 基因(染色体 7q21.3)编码,通过多种机制发挥抗氧化分子的作用。由于氧化应激与偏头痛的发病机制有关,我们研究了 PON1 中的非 synonymous 55LM 和 192QR 多态性与偏头痛风险之间的可能关联。我们使用 TaqMan 单核苷酸多态性分析研究了 197 例偏头痛患者和 220 例健康对照者的 PON1 基因型和等位基因变异的频率。偏头痛患者和对照组之间 PON1 基因型和 PON1 等位基因变异的频率无显著差异,且与性别、偏头痛家族史以及有无先兆无关。PON1 192QQ 基因型和 PON1 192Q 等位基因变异的频率在偏头痛发病较早的患者中显著升高。本研究结果提示,PON1 多态性与西班牙白种人偏头痛的风险无关,尽管 PON1 192Q/Q 基因型和 PON1 192Q 等位基因变异可能与偏头痛的早期发病有关。

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