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首页> 外文期刊>Molecular diagnosis & therapy >Association Between Catechol-O-Methyltransferase-(COMT)Gene Polymorphisms, Parkinson's Disease, and Levodopa Efficacy
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Association Between Catechol-O-Methyltransferase-(COMT)Gene Polymorphisms, Parkinson's Disease, and Levodopa Efficacy

机译:儿茶酚-O-甲基转移酶-(COMT)基因多态性,帕金森氏病和左旋多巴功效之间的关联

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Objectives We investigated the association between catechol-O-methyltransferase (COMT) gene polymorphisms and Parkinson's disease (PD) susceptibility, severity of disease, and levodopa (L-Dopa) efficacy. Subjects and Methods Patients (N = 97) with primary PD and healthy volunteers (N = 102) were recruited. Disease severity was assessed with the Unified Parkinson's Disease Rating Scale (UPDRS) and Hoehn & Yahr grade at 'On stage'. Genomic DNA was extracted from blood cells. Polymerase chain reaction and sequencing were used to detect COMT mutations. Data were analyzed by SPSS 18.0. False discovery rate (FDR) or Bonferroni correction was used if the result showed P < 0.05.
机译:目的我们研究了儿茶酚-O-甲基转移酶(COMT)基因多态性与帕金森氏病(PD)易感性,疾病严重程度和左旋多巴(L-Dopa)疗效之间的关系。受试者与方法招募了原发性PD患者(N = 97)和健康志愿者(N = 102)。疾病严重程度通过“帕金森病统一评分量表”(UPDRS)和“现阶段”的Hoehn&Yahr评分进行评估。从血细胞中提取基因组DNA。聚合酶链反应和测序用于检测COMT突变。通过SPSS 18.0分析数据。如果结果显示P <0.05,则使用错误发现率(FDR)或Bonferroni校正。

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