中国实用医药
中國實用醫藥
중국실용의약
CHINA PRACTICAL MEDICAL
2014年
15期
1-2,3
,共3页
李家鑫%祭健予%李剑%欧俐羽%韦斌垣
李傢鑫%祭健予%李劍%歐俐羽%韋斌垣
리가흠%제건여%리검%구리우%위빈원
脑源性神经营养因子%阿尔茨海默病%功能性多态性
腦源性神經營養因子%阿爾茨海默病%功能性多態性
뇌원성신경영양인자%아이자해묵병%공능성다태성
Brain-derived neurotrophic factor%Alzheimer’s disease%Functional polymorphism
目的:探讨脑源性神经营养因子(BDNF)基因功能性多态(rs6265)与散发性阿尔茨海默病(SAD)发病的相关性。方法选取58例散发性阿尔茨海默患者(SAD组)与52例健康老年人(对照组),用聚合酶链反应-限制性片段长度多态性技术,对BDNF基因rs6265,进行基因型检测,同时利用酶联免疫吸附技术对两组患者的血清BDNF水平进行检测。结果在<60岁的人群中,等位基因(χ2=6.0595, P=0.013)及基因型(χ2=6.0826,P=0.0478)在两组人群中的分布差异有统计学意义,并且SAD的AA基因型患者的血清BDNF水平最低[(14.32±4.21)ng/ml, F=7.2545, P=0.0016]。结论 BDNF基因功能性多态rs6265与SAD发病相关,并且影响其血清BDNF的表达。
目的:探討腦源性神經營養因子(BDNF)基因功能性多態(rs6265)與散髮性阿爾茨海默病(SAD)髮病的相關性。方法選取58例散髮性阿爾茨海默患者(SAD組)與52例健康老年人(對照組),用聚閤酶鏈反應-限製性片段長度多態性技術,對BDNF基因rs6265,進行基因型檢測,同時利用酶聯免疫吸附技術對兩組患者的血清BDNF水平進行檢測。結果在<60歲的人群中,等位基因(χ2=6.0595, P=0.013)及基因型(χ2=6.0826,P=0.0478)在兩組人群中的分佈差異有統計學意義,併且SAD的AA基因型患者的血清BDNF水平最低[(14.32±4.21)ng/ml, F=7.2545, P=0.0016]。結論 BDNF基因功能性多態rs6265與SAD髮病相關,併且影響其血清BDNF的錶達。
목적:탐토뇌원성신경영양인자(BDNF)기인공능성다태(rs6265)여산발성아이자해묵병(SAD)발병적상관성。방법선취58례산발성아이자해묵환자(SAD조)여52례건강노년인(대조조),용취합매련반응-한제성편단장도다태성기술,대BDNF기인rs6265,진행기인형검측,동시이용매련면역흡부기술대량조환자적혈청BDNF수평진행검측。결과재<60세적인군중,등위기인(χ2=6.0595, P=0.013)급기인형(χ2=6.0826,P=0.0478)재량조인군중적분포차이유통계학의의,병차SAD적AA기인형환자적혈청BDNF수평최저[(14.32±4.21)ng/ml, F=7.2545, P=0.0016]。결론 BDNF기인공능성다태rs6265여SAD발병상관,병차영향기혈청BDNF적표체。
Objective To explore the relationship between functional polymorphism of BDNF(brain-derived neurotrophic factor) rs6265 and sporadic Alzheimer’s disease(SAD). Methods Selecting 58 cases of SAD(SAD group) and 52 health old person(control group) as research subjects. Then the genotyped was detected via polymerase chain reaction-restriction fragment length polymorphism and serum levels of BDNF detected by Enzyme-linked Immunosorbent Assay in all cases. Results There was significantly difference in the distributions of alleles(χ2=6.0595,P=0.013) and genotypes(χ2=6.0826,P=0.0478) between the case of SAD group and control group ,and the serum levels of BDNF were lowest for case of AA genotypes in SAD[(14.32±4.21) ng/ml, F=7.2545, P=0.0016]. Conclusion The functional polymorphism of BDNF gene(rs6265) correlated with pathogenesis of SAD and affects the expression of BDNF in serum.