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首页> 外文期刊>Acta neurobiologiae experimentalis >Progression of multiple sclerosis is associated with gender differences in glutathione S-transferase P1 detoxification pathway
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Progression of multiple sclerosis is associated with gender differences in glutathione S-transferase P1 detoxification pathway

机译:多发性硬化的进展与谷胱甘肽S-转移酶P1排毒途径中的性别差异有关

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The impact of glutathione S-transferases (GSTs) detoxification pathway on complex pathogenesis and heterogeneity of clinical findings in multiple sclerosis (MS), particularly the exact correlation between indicators of clinical severity and different GST genotypes, has not yet been fully elucidated. The aim of the study was to assess the relationship between disability level in multiple sclerosis (estimated by Kurtzke Expanded Disability Status Scale), disease progression (estimated by Multiple Sclerosis Severity Score), the level of brain atrophy and lesion load (determined by MRI) and detoxification status (analyzing glutathione S-transferase P1, GSTP1, genotype profile), in a group of 58 MS patients and 68 age/gendermatched controls. The results present the first evidence on significantly higher frequency of GSTP1 C341T polymorphism (C-T transition) in healthy subjects compared to MS patients, suggesting it may act as a moderating factor in developing MS clinical phenotype. Gender-dependent distribution of the C341T polymorphism was found in both MS patients and controls, with higher frequency of C-T transition in females. In addition, preliminary data showed higher proportion of male MS patients with higher median MSSS scores, as well as lower brain atrophy level and lesion load in MS patients carrying the C341T mutation. Observed gender difference in distribution of the C341T polymorphism in MS patients, as well as in disease progression, suggests that GSTP1 detoxification pathway occurs in a gender-dependent manner and could therefore add to clinical severity in male MS patients.
机译:谷胱甘肽S-转移酶(GSTs)的解毒途径对多发性硬化症(MS)中复杂的发病机制和临床发现异质性的影响,特别是临床严重程度指标与不同GST基因型之间的确切相关性,尚未得到充分阐明。该研究的目的是评估多发性硬化症的残疾水平(由Kurtzke扩展残疾状况量表评估),疾病进展(由多发性硬化严重度评分评估),脑萎缩和病变负荷水平(由MRI确定)之间的关系。 58位MS患者和68位年龄/性别匹配的对照组中的排毒状态(分析谷胱甘肽S-转移酶P1,GSTP1和基因型分布)。结果提供了第一个证据,表明健康受试者中GSTP1 C341T多态性(C-T转换)的频率显着高于MS患者,表明它可能是发展MS临床表型的调节因素。在MS患者和对照中均发现了C341T多态性的性别依赖性分布,女性中C-T转换的频率更高。此外,初步数据显示,具有C341T突变的MS患者中,具有较高MSSS中位数评分的男性MS患者比例较高,以及脑萎缩水平和病变负荷较低。在MS患者中观察到C341T多态性分布的性别差异以及疾病进展,表明GSTP1解毒途径以性别依赖性方式发生,因此可能增加男性MS患者的临床严重性。

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