山东大学学报(医学版) ›› 2015, Vol. 53 ›› Issue (4): 71-74.doi: 10.6040/j.issn.1671-7554.0.2014.808
陈思1, 王牧川2, 任楠楠3, 许巍1, 王玲玲1, 栾海辉1, 马俊1, 刘艺鸣1
CHEN Si1, WANG Muchuan2, REN Nannan3, XU Wei1, WANG Lingling1, LUAN Haihui1, MA Jun1, LIU Yiming1
摘要: 目的 探讨Parkin基因多态性与山东省汉族人群帕金森病(PD)发病之间的关系.方法 应用DNA测序及限制性内切酶酶切技术检测山东省汉族人群中145例PD患者(PD组)及126名健康查体者(对照组)Parkin基因的3个单核苷酸多态(Ser167Asn、Val380Leu及Arg366Trp)的等位基因频率,其中PD组包括早发性帕金森病(EOPD)患者67例与晚发性帕金森病(LOPD)患者78例,分析上述3个多态位点PD发病风险中的意义.结果 PD组与对照组的Ser167Asn、Val380Leu及Arg366Trp 3个多态位点等位基因频率均无明显差异;PD组中EOPD患者Ser167Asn、Arg366Trp位点与LOPD患者相比,等位基因频率亦无明显差异;EOPD患者Val380Leu位点与LOPD患者相比,等位基因频率存在显著性差异(P=0.01, OR=3.39, 95%CI:1.287~8.931).结论 山东省汉族人群Parkin基因Ser167Asn、Val380Leu及Arg366Trp多态位点可能与PD的发病无明显相关性,其中Val380Leu可使PD的发病年龄提前.
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