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Association of the functional SNP rs2275294 in ZNF512B with risk of amyotrophic lateral sclerosis and Parkinson's disease in Han Chinese

机译:ZNF512B中功能性SNP rs2275294与肌萎缩性侧索硬化症和帕金森氏病风险的相关性

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摘要

The single nucleotide polymorphism (SNP) rs2275294 of the ZNF512B gene has been reported to be associated with a risk of ALS in the Japanese population. Here we conducted a case-control study examining the possible association of rs2275294 with risk of sporadic ALS and PD in Han Chinese. Our study included 301 patients with ALS and 457 age- and gender-matched controls, as well as 555 patients with PD and 473 age- and gender-matched controls. Subjects were genotyped at rs2275293 using the ligase detection reaction. The genotype distribution of rs2275294 shows significant difference between patients with ALS and the control group according to the dominant model (OR 1.518, 95% CI 1.074-2.145, p = 0.018) and based on alleles (OR 1.249, 95% 1.016-1.534, p = 0.035). Stratification analysis showed a significant difference between females with ALS and female controls based on the dominant model (OR 3.285, 95% CI 1.856-5.815, p < 0.001) or alleles (OR 1.697, 95% CI 1.208-2.383, p = 0.002). In contrast, no significant differences were identified between rs2275294 and patients with PD. In conclusion, our case-control study suggests that the CC genotype and C allele at rs2275294 are associated with increased risk of ALS in Han Chinese, particularly females.
机译:据报道,ZNF512B基因的单核苷酸多态性(SNP)rs2275294与日本人群中ALS的风险有关。在这里,我们进行了一项病例对照研究,研究了rs2275294与中国汉族散发性ALS和PD风险的可能关联。我们的研究包括301例ALS患者和457例年龄和性别匹配的对照,以及555例PD患者和473例年龄和性别匹配的对照。使用连接酶检测反应在rs2275293对受试者进行基因分型。 rs2275294的基因型分布显示,根据优势模型(OR 1.518,95%CI 1.074-2.145,p = 0.018)和基于等位基因(OR 1.249,95%1.016-1.53​​4, p = 0.035)。分层分析显示,基于优势模型(OR 3.285,95%CI 1.856-5.815,p <0.001)或等位基因(OR 1.697,95%CI 1.208-2.383,p = 0.002),患有ALS的女性和女性对照组之间存在显着差异。 。相反,rs2275294与PD患者之间未发现明显差异。总之,我们的病例对照研究表明,rs2275294的CC基因型和C等位基因与汉族人(尤其是女性)患ALS的风险增加相关。

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