中华神经医学杂志
中華神經醫學雜誌
중화신경의학잡지
CHINESE JOURNAL OF NEUROMEDICINE
2011年
9期
879-882
,共4页
冯骏%肖新莉%刘哲%秦皓%刘丽华%张敏%张波%刘亚民
馮駿%肖新莉%劉哲%秦皓%劉麗華%張敏%張波%劉亞民
풍준%초신리%류철%진호%류려화%장민%장파%류아민
动脉粥样硬化%颈动脉%转化生长因子β1%内皮素转换酶-1b%多态性,单核苷酸
動脈粥樣硬化%頸動脈%轉化生長因子β1%內皮素轉換酶-1b%多態性,單覈苷痠
동맥죽양경화%경동맥%전화생장인자β1%내피소전환매-1b%다태성,단핵감산
Atherosclerosis%Carotid artery%Transforming growth factor 31%Endothelin converting enzyme-lb%Polymorphism,single nucleotide
目的探讨转化生长因子β1基因与内皮素转换酶-1b基因多态性和颈动脉粥样硬化易感性的关联情况。 方法选择西安交通大学医学院第一附属医院神经内科自2006年1月至2010年12月收治的231例脑梗死住院患者为患者组,同期社区健康自愿参与研究者231例为对照组,运用PCR及单核苷酸多态性技术分析2组成员转化生长网子β1基因与内皮素转换酶-1b基因多态性分型,比较2组间基因和基因型差异。 结果患者组和对照组转化生长因子β1基因的rs51695112位点基因和基因型差异有统计学意义(x2=6.120、6.890,P=0.045、0.033),G等位基因和G/G基因型为颈动脉粥样硬化易感性的高危因素(OR=1.320、1.410);患者组和对照组内皮素转换酶-1b基因rs32570233位点基因和基因型差异有统计学意义(x2=6.320、7.180,P=0.041、0.022),A等位基因和A/A基因型为颈动脉粥样硬化易感性的高危因素(OR=1.470、1.530)。 结论转化生长因子β1基因、内皮素转换酶-1b基因多态性与颈动脉粥样硬化相关联。
目的探討轉化生長因子β1基因與內皮素轉換酶-1b基因多態性和頸動脈粥樣硬化易感性的關聯情況。 方法選擇西安交通大學醫學院第一附屬醫院神經內科自2006年1月至2010年12月收治的231例腦梗死住院患者為患者組,同期社區健康自願參與研究者231例為對照組,運用PCR及單覈苷痠多態性技術分析2組成員轉化生長網子β1基因與內皮素轉換酶-1b基因多態性分型,比較2組間基因和基因型差異。 結果患者組和對照組轉化生長因子β1基因的rs51695112位點基因和基因型差異有統計學意義(x2=6.120、6.890,P=0.045、0.033),G等位基因和G/G基因型為頸動脈粥樣硬化易感性的高危因素(OR=1.320、1.410);患者組和對照組內皮素轉換酶-1b基因rs32570233位點基因和基因型差異有統計學意義(x2=6.320、7.180,P=0.041、0.022),A等位基因和A/A基因型為頸動脈粥樣硬化易感性的高危因素(OR=1.470、1.530)。 結論轉化生長因子β1基因、內皮素轉換酶-1b基因多態性與頸動脈粥樣硬化相關聯。
목적탐토전화생장인자β1기인여내피소전환매-1b기인다태성화경동맥죽양경화역감성적관련정황。 방법선택서안교통대학의학원제일부속의원신경내과자2006년1월지2010년12월수치적231례뇌경사주원환자위환자조,동기사구건강자원삼여연구자231례위대조조,운용PCR급단핵감산다태성기술분석2조성원전화생장망자β1기인여내피소전환매-1b기인다태성분형,비교2조간기인화기인형차이。 결과환자조화대조조전화생장인자β1기인적rs51695112위점기인화기인형차이유통계학의의(x2=6.120、6.890,P=0.045、0.033),G등위기인화G/G기인형위경동맥죽양경화역감성적고위인소(OR=1.320、1.410);환자조화대조조내피소전환매-1b기인rs32570233위점기인화기인형차이유통계학의의(x2=6.320、7.180,P=0.041、0.022),A등위기인화A/A기인형위경동맥죽양경화역감성적고위인소(OR=1.470、1.530)。 결론전화생장인자β1기인、내피소전환매-1b기인다태성여경동맥죽양경화상관련。
Objective To study the relationship between polymorphisms of transforming growth factor β1 gene and endothelin converting enzyme-1b gene and susceptibility of carotid atherosclerosis. Methods Two hundred and thirty-one patients with carotid atherosclerosis, admitted to and received treatment in our hospital from January 2006 to December 2010, and 231 healthy volunteers were chosen in our study. The polymorphisms of transforming growth factor β1 gene and endothelin converting enzyme-lb gene in these 2 groups were detected with PCR and single nucleotide polymorphism; the differences of these gene and genotype between the 2 groups were compared by statistical analysis.Results The gene and genotype of transforming growth factor β1 gene at rs51695112 locus were significantly different between patient group and control group (x2=6.120, 6.890;P=0.045, 0.033, respectively); the G allele and G/G genotype were risk factors of carotid atherosclerosis susceptibility (OR=1.320, 1.410, respectively). The gene and genotype of endothelin converting enzyme-1b gene at rs32570233 locus were significantly different between the patient group and the control group (x2=6.320, 7.180; P=0.041, 0.022); the A allele and A/A genotype were the risk factors of carotid atherosclerosis susceptibility (OR=1.470, 1.530, respectively). Conclusion There is an association between polymorphisms of transforming growth factor β 1 gene and endothelin converting enzyme-1b gene and carotid atherosclerosis.