中华老年医学杂志
中華老年醫學雜誌
중화노년의학잡지
Chinese Journal of Geriatrics
2012年
11期
994-997
,共4页
张宁%王振华%陈玉珺%王夏红%许予明
張寧%王振華%陳玉珺%王夏紅%許予明
장저%왕진화%진옥군%왕하홍%허여명
缺血性脑病%纤溶酶原激活抑制物1%多态性,单核苷酸%汉族
缺血性腦病%纖溶酶原激活抑製物1%多態性,單覈苷痠%漢族
결혈성뇌병%섬용매원격활억제물1%다태성,단핵감산%한족
Ischemic encephalopathy%Plasminogen activator inhibitor-1%Polymorphism,single nucleotide%Han nationality
目的 探讨河南汉族老年患者纤溶酶原激活抑制物(PAI-1)基因多态性与缺血性脑血管病的关系及其与相关的危险因素的相互作用. 方法 应用病例对照研究方法,选取408例缺血性脑血管病患者以及年龄、性别匹配的418例健康对照人群为研究对象,采用聚合酶链式反应-限制性片段多态性(PCR-RFLP)法进行PAI-1-844G/A多态性位点检测. 结果 患者组PAI-1-844G/A位点AA、AG、GG基因型频率依次为18.1%、41.4%、40.4%,对照组分别为15.8%、47.4%、36.8%;患者组和对照组A等位基因频率分别为38.8%、39.5%,G等位基因频率分别为61.2%、60.5%.PAI-1-844G/A位点基因型和等位基因频率差异均无统计学意义(P>0.05).PAI-1基因844G/A位点多态性的不同基因型与缺血性脑血管病患者的血压、血糖、血浆同型半胱氨酸(Hcy)水平等指标间无相关性(均P>0.05). 结论 PAI-1基因-844G/A位点多态性可能不是河南汉族老年人群缺血性脑血管病发病的独立危险因素.
目的 探討河南漢族老年患者纖溶酶原激活抑製物(PAI-1)基因多態性與缺血性腦血管病的關繫及其與相關的危險因素的相互作用. 方法 應用病例對照研究方法,選取408例缺血性腦血管病患者以及年齡、性彆匹配的418例健康對照人群為研究對象,採用聚閤酶鏈式反應-限製性片段多態性(PCR-RFLP)法進行PAI-1-844G/A多態性位點檢測. 結果 患者組PAI-1-844G/A位點AA、AG、GG基因型頻率依次為18.1%、41.4%、40.4%,對照組分彆為15.8%、47.4%、36.8%;患者組和對照組A等位基因頻率分彆為38.8%、39.5%,G等位基因頻率分彆為61.2%、60.5%.PAI-1-844G/A位點基因型和等位基因頻率差異均無統計學意義(P>0.05).PAI-1基因844G/A位點多態性的不同基因型與缺血性腦血管病患者的血壓、血糖、血漿同型半胱氨痠(Hcy)水平等指標間無相關性(均P>0.05). 結論 PAI-1基因-844G/A位點多態性可能不是河南漢族老年人群缺血性腦血管病髮病的獨立危險因素.
목적 탐토하남한족노년환자섬용매원격활억제물(PAI-1)기인다태성여결혈성뇌혈관병적관계급기여상관적위험인소적상호작용. 방법 응용병례대조연구방법,선취408례결혈성뇌혈관병환자이급년령、성별필배적418례건강대조인군위연구대상,채용취합매련식반응-한제성편단다태성(PCR-RFLP)법진행PAI-1-844G/A다태성위점검측. 결과 환자조PAI-1-844G/A위점AA、AG、GG기인형빈솔의차위18.1%、41.4%、40.4%,대조조분별위15.8%、47.4%、36.8%;환자조화대조조A등위기인빈솔분별위38.8%、39.5%,G등위기인빈솔분별위61.2%、60.5%.PAI-1-844G/A위점기인형화등위기인빈솔차이균무통계학의의(P>0.05).PAI-1기인844G/A위점다태성적불동기인형여결혈성뇌혈관병환자적혈압、혈당、혈장동형반광안산(Hcy)수평등지표간무상관성(균P>0.05). 결론 PAI-1기인-844G/A위점다태성가능불시하남한족노년인군결혈성뇌혈관병발병적독립위험인소.
Objective To investigate the association between gene polymorphism of plasminogen activator inhibitor (PAI-1)and ischemic cerebrovascular disease in aged people of Henan Han nationality.Methods A case control method was used,including 408 patients with ischemic cerebrovascular disease and 418 age and gender matched healthy controls.Polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) method was used to determine the distribution of allele and genotype frequencies of PAI-1 844G/A.Results In patient group,the gene frequencies of AA,AG,GG were 18.1%,41.4%,40.4%,and the A and G allele frequencies were 38.8% and 61.2%,respectively.In the control group,the gene frequencies of AA,AG,GG were 15.8%,47.4%,36.8%,and the A and G allele frequencies were 39.5% and 60.5%.There were no significant differences in the frequencies of genotypes and alleles between the two groups (P>0.05).The different genotypes of 844G/A of PAI-1 gene were not associated with hypertension,hyperglycemia,plasma homocysteic acid levels (P > 0.05).Conclusions PAI-1 gene-844G/A polymorphism may not be independent risk factor of ischemic cerebrovascular disease in aged people of Henan Han nationality.