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首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Alpha synuclein promoter and risk of Parkinson's disease: microsatellite and allelic size variability.
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Alpha synuclein promoter and risk of Parkinson's disease: microsatellite and allelic size variability.

机译:α突触核蛋白启动子和帕金森氏病的风险:微卫星和等位基因大小变异性。

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摘要

Polymorphism of the alpha synuclein promoter region (non-amyloid component of plaques (NACP)-Rep1) is associated with an increased risk of Parkinson's disease (PD) in three separate studies. We studied NACP-Rep1 polymorphism in two independent case control studies in our population. In study one, 104 PD and 104 age, gender and race matched controls; and in study two, 102 PD and 102 age, gender and race matched controls were examined separately. The results of both studies were analyzed independent of one another. We found three polymorphic alleles (designated 0, 1, 2). In study one, the frequency of allele 2 was significantly higher in PD patients as compared to healthy controls (0.37 versus 0.23, P=0.01, X(2)=9.98). In study two, the frequency of allele 2 was similar between PD and controls (0.31 versus 0.33, P=1.00, X(2)=0.30). There was a non-significant higher allele 2 frequency in PD when both studies were analyzed together (0.34 versus 0.28, P=0.20, X(2)=3.4). No significant differences of the various genotypes between PD and controls were found. However there were differences of the mixed dinucleotide repeats sequences for similar homozygous genotypes. Variability of the microsatellite region and potential interacting factors that could affect alpha synuclein gene transcription should be further examined.
机译:在三项单独的研究中,α突触核蛋白启动子区域(斑块的非淀粉样成分(NACP)-Rep1)的多态性与帕金森氏病(PD)的风险增加有关。我们在人群中的两个独立的病例对照研究中研究了NACP-Rep1多态性。在研究一中,有104位PD和104位年龄,性别和种族相匹配的对照组;在研究中,分别检查了102位PD和102位年龄,性别和种族匹配的对照。两项研究的结果相互独立地进行了分析。我们发现了三个多态性等位基因(指定为0、1、2)。在研究一中,与健康对照组相比,PD患者的等位基因2频率显着更高(0.37对0.23,P = 0.01,X(2)= 9.98)。在研究二中,PD和对照之间的等位基因2频率相似(0.31对0.33,P = 1.00,X(2)= 0.30)。在一起分析这两项研究时,PD中无显着性较高的等位基因2频率(0.34对0.28,P = 0.20,X(2)= 3.4)。在PD和对照之间没有发现各种基因型的显着差异。然而,对于相似的纯合基因型,混合的二核苷酸重复序列存在差异。微卫星区域的变化和可能影响α突触核蛋白基因转录的潜在相互作用因子应进一步检查。

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