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Association Analysis of NALCN Polymorphisms rs1338041 and rs61973742 in a Chinese Population with Isolated Cervical Dystonia

机译:中国人孤立性宫颈肌张力障碍人群NALCN基因多态性rs1338041和rs61973742的关联分析

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摘要

Background. A genome-wide association study (GWAS) demonstrated a possible association between cervical dystonia (CD) and a sodium leak channel, nonselective (NALCN) gene. However, the association between NALCN and CD was largely unknown in Asian population. The present study was carried out to examine the associations between the two single nucleotide polymorphisms (SNPs) rs1338041 and rs61973742 in the NALCN gene and CD in a Chinese population. Methods. In a cohort of 201 patients with isolated CD, we genotyped the two SNPs rs1338041 and rs61973742 using polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP). We also included 289 unrelated, age- and sex-matched healthy controls (HCs) from the same region. Result. No significant differences were observed in either the genotype distributions or the minor allele frequencies (MAFs) of the two SNPs between the CD patients and the HCs. There were no significant differences between early-onset and late-onset CD patients, between patients with and without a positive family history of dystonia, or between patients with and without tremor or sensory tricks. Conclusion. Lack of association between the SNPs of NALCN and CD suggests that the SNPs of NALCN do not play a role in CD in a Chinese population.
机译:背景。全基因组关联研究(GWAS)显示了颈肌张力障碍(CD)与钠泄漏通道非选择性(NALCN)基因之间的可能关联。但是,在亚洲人群中,NALCN和CD之间的关联很大程度上未知。本研究旨在检查中国人群中NALCN基因中的两个单核苷酸多态性(SNP)rs1338041和rs61973742与CD之间的关联。方法。在201例分离性CD患者中,我们使用聚合酶链反应限制片段长度多态性(PCR-RFLP)对两个SNP rs1338041和rs61973742进行了基因分型。我们还纳入了来自同一地区的289个年龄,性别匹配的不相关健康对照(HCs)。结果。在CD患者和HCs之间,两个SNP的基因型分布或次要等位基因频率(MAF)均未观察到显着差异。在早期和晚期CD患者之间,有和没有肌张力障碍家族史的患者之间,有和没有震颤或感觉技巧的患者之间没有显着差异。结论。 NALCN和CD的SNP之间缺乏关联,这表明NALCN的SNP在中国人群的CD中不起作用。

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