中国医师进修杂志
中國醫師進脩雜誌
중국의사진수잡지
CHINESE JOURNAL OF POSTGRADUATES OF MEDICINE
2008年
22期
12-15
,共4页
丁明%郑金旭%严玉兰%蔡后荣%汪毅%仇铁峰%卞秀娟
丁明%鄭金旭%嚴玉蘭%蔡後榮%汪毅%仇鐵峰%卞秀娟
정명%정금욱%엄옥란%채후영%왕의%구철봉%변수연
肺纤维化%白细胞介素13%呼吸功能试验%基因多态性
肺纖維化%白細胞介素13%呼吸功能試驗%基因多態性
폐섬유화%백세포개소13%호흡공능시험%기인다태성
Pulmonary fibrosis%Interleukin-13%Respiratory function tests%Gene polymorphism
目的 探讨白细胞介素13(IL-13)基因启动子区-1112(C/T)位点基因多态性与特发性肺纤维化(IPF)的相关性. 方法 研究组IPF患者70例,根据肺功能分为3个亚组,以A(弥散功能轻度下降,22例)、B(弥散功能中度下降,20例)、C(弥散功能重度下降,28例)组表示,80例健康体检者作为对照组.外周血提取基因组DNA,采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)检测IL-13基因启动子区-1112(C/T)位点的基因多态性. 结果 研究组IL-13基因启动子区-1112(C/T)位点的基因多态性分布为CC纯合子28例(40.0%),TT纯合子6例(8.6%),CT杂合子36例(51.4%);对照组CC纯合子30例(37.5%),TT纯合子11例(13.8%),CT杂合子39例(48.8%),-1112(C/T)位点等位基因C、T在两组间分布及三种基因型之间构成比比较差异无统计学意义(P>0.05).A组CT和TT基因型共9例(40.9%),B组CT和TT基因型共10例(50.0%),C组CT和TT基因型共23例(82.1%),三组间比较差异有统计学意义(P均<0.05). 结论 IL-13基因启动子区-1112(C/T)位点基因多态性与IPF的发病无关,但与其肺弥散功能的损害程度有关.
目的 探討白細胞介素13(IL-13)基因啟動子區-1112(C/T)位點基因多態性與特髮性肺纖維化(IPF)的相關性. 方法 研究組IPF患者70例,根據肺功能分為3箇亞組,以A(瀰散功能輕度下降,22例)、B(瀰散功能中度下降,20例)、C(瀰散功能重度下降,28例)組錶示,80例健康體檢者作為對照組.外週血提取基因組DNA,採用聚閤酶鏈反應-限製性片段長度多態性(PCR-RFLP)檢測IL-13基因啟動子區-1112(C/T)位點的基因多態性. 結果 研究組IL-13基因啟動子區-1112(C/T)位點的基因多態性分佈為CC純閤子28例(40.0%),TT純閤子6例(8.6%),CT雜閤子36例(51.4%);對照組CC純閤子30例(37.5%),TT純閤子11例(13.8%),CT雜閤子39例(48.8%),-1112(C/T)位點等位基因C、T在兩組間分佈及三種基因型之間構成比比較差異無統計學意義(P>0.05).A組CT和TT基因型共9例(40.9%),B組CT和TT基因型共10例(50.0%),C組CT和TT基因型共23例(82.1%),三組間比較差異有統計學意義(P均<0.05). 結論 IL-13基因啟動子區-1112(C/T)位點基因多態性與IPF的髮病無關,但與其肺瀰散功能的損害程度有關.
목적 탐토백세포개소13(IL-13)기인계동자구-1112(C/T)위점기인다태성여특발성폐섬유화(IPF)적상관성. 방법 연구조IPF환자70례,근거폐공능분위3개아조,이A(미산공능경도하강,22례)、B(미산공능중도하강,20례)、C(미산공능중도하강,28례)조표시,80례건강체검자작위대조조.외주혈제취기인조DNA,채용취합매련반응-한제성편단장도다태성(PCR-RFLP)검측IL-13기인계동자구-1112(C/T)위점적기인다태성. 결과 연구조IL-13기인계동자구-1112(C/T)위점적기인다태성분포위CC순합자28례(40.0%),TT순합자6례(8.6%),CT잡합자36례(51.4%);대조조CC순합자30례(37.5%),TT순합자11례(13.8%),CT잡합자39례(48.8%),-1112(C/T)위점등위기인C、T재량조간분포급삼충기인형지간구성비비교차이무통계학의의(P>0.05).A조CT화TT기인형공9례(40.9%),B조CT화TT기인형공10례(50.0%),C조CT화TT기인형공23례(82.1%),삼조간비교차이유통계학의의(P균<0.05). 결론 IL-13기인계동자구-1112(C/T)위점기인다태성여IPF적발병무관,단여기폐미산공능적손해정도유관.
Objective To investigate the potential correlation of interleukin-13(IL-13)gene promoter-1112(C/T)polymorphism with idiopathic pulmonary fibrosis(IPF).Methods According to the diffusion for carbon monoxide(DLCO)or diffusion coefficient(DLCO/VA),70 patients with IPF(investigation group)divided into three groups(group A,group B and group C)and 80 healthy controls(control group)were investigated.The IL-13 gene promoter-1112(C/T)polymorphism was genotyped by polymerase chain reaction-restriction fragment length polymorphism(PCR-RFLP)analysis.The pulmonary diffusion function was measured by DLCO and DLCONA.Results The IL-13 gene promoter-1112(C/T)polymorphism frequency of the homozygous CC,homozygous TT and hetorozygous CT was 40.0%(28 cases),8.6%(6 cases)and 51.4%(36 cases)in investigation group.The frequency of the homozygous CC,homozygous TT and heterozygous CT was 37.5%(30 cases),13.8%(11 cases) and 48.8%(39 cases)in control group.There were no significant differences in the distribution of the three genotypes between the two groups (P>0.05).The frequency of the heterozygous CT and homozygous TT was 40.9%(9/22) in group A,50.0%(10/20)in group B and 82.1%(23/28)in group C.There were significant differences in the distribution of the three genotypes among group A,B and C(P<0.05).Conclusion IL-13 gene promoter-1112(C/T)polymorphism may not be involved in the development of the IPF and may be related to pulmonary diffusion function.