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[新疆维吾尔族和汉族多巴胺β-羟化酶基因多态性与帕金森病的关联]

[Association between polymorphism of dopamine β-hydroxylase gene and Parkinson's disease in Uygurs and Hans of Xinjiang].

作者信息

Li Yanyun, Zhang Xiaoying, Han Xihe, Guo Miao, Zou Mei, Wang Linlin, Li Yan, Xiao Yan, Zeng Wenjing, Song Qiuxia

机构信息

Department of Neurology, General Hospital, Xinjiang Production & Construction Corps, Urumqi 830002, China.

Department of Neurology, General Hospital, Xinjiang Production & Construction Corps, Urumqi 830002, China. Email:

出版信息

Zhonghua Yi Xue Za Zhi. 2014 Mar 25;94(11):808-12.

Abstract

OBJECTIVE

To explore the relationship between dopamine β-hydroxylase gene polymorphisms and Parkinson's disease (PD) in Uygurs and Hans populations of Xinjiang.

METHODS

The polymorphisms of DBH gene were determined by polymerase chain-reaction restriction fragment length polymorphism (PCR-RFLP) in 239 PD patients (including 100 Uygurs and 141 Hans) and 232 health controls (including 103 Uygurs and 129 Hans).

RESULTS

The genotypic or allelic distribution of DBH gene had significant differences between PD and control groups in both Uygur and Han populations (P < 0.05). The genotypic or allelic frequencies were significantly different between Han PD and control groups (P < 0.05). The genotypic or allelic frequencies in those aged 65 years or above were significantly different from that in others (P < 0.05). There was a significant increase of PD in A2 allele carriers (OR = 1.965, P < 0.05). And the frequencies of A2 allele in female PD patients were higher than those in female controls (P < 0.05) and A2 allele carriers had a significant increase of PD (OR = 1.696, P < 0.05).

CONCLUSION

Different between Uygurs and Hans of Xinjiang, DBH5 TaqI polymorphisms may be associated with PD in Hans. A2 allele carriers are often found in females and those aged 65 years or above.

摘要

目的

探讨新疆维吾尔族和汉族人群中多巴胺β-羟化酶基因多态性与帕金森病(PD)的关系。

方法

采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法,对239例PD患者(其中维吾尔族100例,汉族141例)和232例健康对照者(其中维吾尔族103例,汉族129例)的DBH基因多态性进行检测。

结果

维吾尔族和汉族的PD组与对照组之间DBH基因的基因型或等位基因分布均有显著差异(P<0.05)。汉族PD组与对照组之间的基因型或等位基因频率有显著差异(P<0.05)。65岁及以上人群的基因型或等位基因频率与其他人群有显著差异(P<0.05)。A2等位基因携带者的PD发生率显著增加(OR=1.965,P<0.05)。女性PD患者中A2等位基因频率高于女性对照组(P<0.05),且A2等位基因携带者的PD发生率显著增加(OR=1.696,P<0.05)。

结论

新疆维吾尔族和汉族之间存在差异,DBH5 TaqI多态性可能与汉族的PD有关。A2等位基因携带者常见于女性及65岁及以上人群。

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