中华神经科杂志
中華神經科雜誌
중화신경과잡지
Chinese Journal of Neurology
2008年
5期
339-342
,共4页
宋新建%王枫%周勇%李晓波%沈晓明%丁海霞%姚娟%邓晓萱%丁新生
宋新建%王楓%週勇%李曉波%瀋曉明%丁海霞%姚娟%鄧曉萱%丁新生
송신건%왕풍%주용%리효파%침효명%정해하%요연%산효훤%정신생
脑梗塞%蛋白激酶C%多态性,单核苷酸%疾病遗传易感性
腦梗塞%蛋白激酶C%多態性,單覈苷痠%疾病遺傳易感性
뇌경새%단백격매C%다태성,단핵감산%질병유전역감성
Brain infarction%Protein kinase C%Polymorphism,single nucleotide%Genetic predisposition to disease
目的 探讨江苏汉族人群蛋白激酶cη(PRKCH)基因1425G/A单核苷酸多态与脑梗死的关系.方法 采用病例-对照的方法,选取255例脑梗死患者和225例其他疾病患者或健康体检者为对照,应用PCR扩增产物直接测序法筛查PRKCH基因1425G/A单核苷酸多态,对相关资料编码后输入SPSS 13.0统计学软件进行数据分析.结果 在脑梗死组中GA+AA基因型频率(56.86%)和A等位基因频率(36.27%)明显高于对照组(44.44%和24.67%;χ2=7.377,P=0.007;χ2=15.104,P<0.01);对脑梗死组的不同亚型进一步分析发现,腔隙性脑梗死亚组该位点基凶型(63.09%)和等位摹因频率(40.27%)分布与对照组(44.44%和24.67%)相比,差异有统计学意义(χ2=11.744,P=0.01;χ2=20.445,P<0.01).Logistic回归分析显示,高血压、糖尿病、高血脂和A等位基因是江苏汉族人群腔隙性脑梗死的独立危险因素.结论 PRKCH基因1425G/A多态可能与脑梗死发生相关,尤其是与腔隙性脑梗死的发生相关.
目的 探討江囌漢族人群蛋白激酶cη(PRKCH)基因1425G/A單覈苷痠多態與腦梗死的關繫.方法 採用病例-對照的方法,選取255例腦梗死患者和225例其他疾病患者或健康體檢者為對照,應用PCR擴增產物直接測序法篩查PRKCH基因1425G/A單覈苷痠多態,對相關資料編碼後輸入SPSS 13.0統計學軟件進行數據分析.結果 在腦梗死組中GA+AA基因型頻率(56.86%)和A等位基因頻率(36.27%)明顯高于對照組(44.44%和24.67%;χ2=7.377,P=0.007;χ2=15.104,P<0.01);對腦梗死組的不同亞型進一步分析髮現,腔隙性腦梗死亞組該位點基兇型(63.09%)和等位摹因頻率(40.27%)分佈與對照組(44.44%和24.67%)相比,差異有統計學意義(χ2=11.744,P=0.01;χ2=20.445,P<0.01).Logistic迴歸分析顯示,高血壓、糖尿病、高血脂和A等位基因是江囌漢族人群腔隙性腦梗死的獨立危險因素.結論 PRKCH基因1425G/A多態可能與腦梗死髮生相關,尤其是與腔隙性腦梗死的髮生相關.
목적 탐토강소한족인군단백격매cη(PRKCH)기인1425G/A단핵감산다태여뇌경사적관계.방법 채용병례-대조적방법,선취255례뇌경사환자화225례기타질병환자혹건강체검자위대조,응용PCR확증산물직접측서법사사PRKCH기인1425G/A단핵감산다태,대상관자료편마후수입SPSS 13.0통계학연건진행수거분석.결과 재뇌경사조중GA+AA기인형빈솔(56.86%)화A등위기인빈솔(36.27%)명현고우대조조(44.44%화24.67%;χ2=7.377,P=0.007;χ2=15.104,P<0.01);대뇌경사조적불동아형진일보분석발현,강극성뇌경사아조해위점기흉형(63.09%)화등위모인빈솔(40.27%)분포여대조조(44.44%화24.67%)상비,차이유통계학의의(χ2=11.744,P=0.01;χ2=20.445,P<0.01).Logistic회귀분석현시,고혈압、당뇨병、고혈지화A등위기인시강소한족인군강극성뇌경사적독립위험인소.결론 PRKCH기인1425G/A다태가능여뇌경사발생상관,우기시여강극성뇌경사적발생상관.
Objective To explore the association between 1425G/A single nucleotide polymorphism(SNP)of protein kinase Cη gene(PRKCH)and cerebral infarction in Jiangsu Han population.Methods 255 patients with cerebral infarction and 225 controls were recruited in our case-control study.The 1425G/A in PRKCH gene was detected by direct sequencing of PCR products.Data were coded and entered in SPSS Windows(version 13.0).Results The frequencies of the GA+AA genotypes(56.86%)and A allele (36.27%)in cerebral infarct group were significantly higher than those in control group(44.44%and24.67%.χ2=7.377,P=0.007 and χ2=15.104,P<0.01).Further analysis indicated that the genotypes(63.09%)and alleles(40.27%)frequencies were statistically different between lacunar infarction subtype and controls(44.44%and 24.67%;χ2=11.744,P=0.Ol and χ2=20.445,P<0.01).Logistic regression analysis revealed that hypertension,diabetes mellitus.hyperlipidemia and the A allele of 1425G/A polymorphism were independent risky factors for lacunar infarction.Conclusions The SNP 1425G/A in PRKCH is closely associated with cerebral infarction.particularly with lacunar infarction.