中华神经科杂志
中華神經科雜誌
중화신경과잡지
Chinese Journal of Neurology
2008年
9期
585-588
,共4页
杨娟%谢正祥%王学峰%张婧%席志芹%黄祖春
楊娟%謝正祥%王學峰%張婧%席誌芹%黃祖春
양연%사정상%왕학봉%장청%석지근%황조춘
癫(癎)%谷胱甘肽转移酶%多态性,单核苷酸%脑电描记术
癲(癎)%穀胱甘肽轉移酶%多態性,單覈苷痠%腦電描記術
전(간)%곡광감태전이매%다태성,단핵감산%뇌전묘기술
Epilepsy%Glutathione transferase%Polymorphism,single nucleotide%Electroencephalography
目的 探讨谷胱甘肽硫转移酶(GST)-pi基因3个位点(lle105Val、Ala114Val、Asp147Tyr)的单核苷酸多态性(SNP)与癫(癎)及难治性癫(癎)易息性的相关性.方法 采用等位基因特异性引物PCR技术检测GST-pi SNP,分析其在隐源性癫(癎)患者中的频率分布特征及其相关性.结果 在非难治性癫(癎)组中GST-pi基因变异的SNP在3个位点分布频率分别为59.62%、55.32%、50.94%,在难治性癫(癎)组中为58.33%、51.19%、45.92%.两组中GST-pi的3个位点变异基因型及变异等位基因分布频率均较健康对照组高(P<0.01).典型癫(癎)波脑电图组与不典型的异常脑电图组的基因型频率分布比较差异有统计学意义(F=0.0294、8.867×10-6、1.366×10-5,P<0.05).结论 GST-pi基因任一位点突变与癫(癎)易患性均具有相关性,且脑电图呈典型癫(癎)波,但与癫(癎)是否发展为难治性癫(癎)无关.
目的 探討穀胱甘肽硫轉移酶(GST)-pi基因3箇位點(lle105Val、Ala114Val、Asp147Tyr)的單覈苷痠多態性(SNP)與癲(癎)及難治性癲(癎)易息性的相關性.方法 採用等位基因特異性引物PCR技術檢測GST-pi SNP,分析其在隱源性癲(癎)患者中的頻率分佈特徵及其相關性.結果 在非難治性癲(癎)組中GST-pi基因變異的SNP在3箇位點分佈頻率分彆為59.62%、55.32%、50.94%,在難治性癲(癎)組中為58.33%、51.19%、45.92%.兩組中GST-pi的3箇位點變異基因型及變異等位基因分佈頻率均較健康對照組高(P<0.01).典型癲(癎)波腦電圖組與不典型的異常腦電圖組的基因型頻率分佈比較差異有統計學意義(F=0.0294、8.867×10-6、1.366×10-5,P<0.05).結論 GST-pi基因任一位點突變與癲(癎)易患性均具有相關性,且腦電圖呈典型癲(癎)波,但與癲(癎)是否髮展為難治性癲(癎)無關.
목적 탐토곡광감태류전이매(GST)-pi기인3개위점(lle105Val、Ala114Val、Asp147Tyr)적단핵감산다태성(SNP)여전(간)급난치성전(간)역식성적상관성.방법 채용등위기인특이성인물PCR기술검측GST-pi SNP,분석기재은원성전(간)환자중적빈솔분포특정급기상관성.결과 재비난치성전(간)조중GST-pi기인변이적SNP재3개위점분포빈솔분별위59.62%、55.32%、50.94%,재난치성전(간)조중위58.33%、51.19%、45.92%.량조중GST-pi적3개위점변이기인형급변이등위기인분포빈솔균교건강대조조고(P<0.01).전형전(간)파뇌전도조여불전형적이상뇌전도조적기인형빈솔분포비교차이유통계학의의(F=0.0294、8.867×10-6、1.366×10-5,P<0.05).결론 GST-pi기인임일위점돌변여전(간)역환성균구유상관성,차뇌전도정전형전(간)파,단여전(간)시부발전위난치성전(간)무관.
Objective To study the distribution patterns of the SNPs for the 3 sites (Ⅱe105Val, Ala114Val and Asp147Tyr) of glutathione S-transferase pi (GST-pi) in epilepsy patients without definite etiological factors. Methods At the same time, the possible relationship of GST-pi gene mutation with the vulnerability of drug-resistant epilepsy, drug-responsive epilepsy and EEG feature were explored. The SNPs of GST-pi for healthy people, drug-responsive epilepsy patients and drug-resistant epilepsy patients were genotyped by sequence-specific primers (SSP)-based PCR technologies (PCR-SSP). Results In drugresponsive epilepsy group, the frequency for 3 sites of mutated SNP of GST-pi was 59.62%, 55.32% and 50.94%, while it was 58.33%, 51.19% and 45.92% in drug-resistant epilepsy group. The difference of genotype and allele between normal group and foregoing epilepsy group was significant ( P<0.01 ), but no difference was found between drug-respensive epilepsy group and drug-resistant epilepsy group ( P>0.05 ). There was a difference of genotype distribution between groups with typical and untypical epilepsy EEG ( F = 0.0294, 8.867 × 10-6, 1.366 × 10-5, P<0.05 ). Conclusions The results indicate that the SNPs of GST-pi are associated with an increased risk of epilepsy, but not associated with an increased risk of drugresistant epilepsy. The patients present EEG characteristic of typical epilepsy.