MICA基因第5外显子与乙肝后肝硬变的相关性研究  被引量:2

The correlation between liver cirrhosis by hepatitis B and MICA exon 5 gene

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作  者:姜孝新[1] 蒋艳[1] 李艳雯[1] 伍小平[1] 

机构地区:[1]南华大学附属第一医院检验科,衡阳市421001

出  处:《实用检验医师杂志》2013年第2期76-78,108,共4页Chinese Journal of Clinical Pathologist

基  金:基金项目:国家自然基金项目资助(31200141);湖南省教育厅项目资助(11C1110);湖南省自然基金项目资助(08JJ3060)

摘  要:目的研究MICA基因多态性、sMICA分子与乙肝后肝硬化(livercirrhosis,LC)的相关性。方法采用MICA—STR微卫星基因分型技术检测101例HBsAg阳性LC患者和141例健康对照者MICA基因第5外显子的基因多态性,并进行统计学分析。结果在101例湖南汉族HBsAg阳性LC患者中检测到5种MICA基因第5外显子等位基因,频率分别为:MICA*A4(10.9%),MICA*A5(37.1%),MICA*A5.1(34.2%),MICA*A6(7.4%),MICA*A9(10.4%)。15种基因型分别为MICA*A4/A4,MICA*A4/A5.MICA*A4/A5.1.MICA*A4/A6,MICA*A4/A9,MICA*A5/A5,MICA*A5/A5.1,MICA*A5/A6.MICA*A5/A9,MICA*A5.1/A5.1,MICA*A5.1/A6,MICA*A5.1/A9,MICA*A6/A6,MICA*A6/A9,MICA*A9/A9。MICA*A5.1基因与LC发病正相关(P=0.042),OR值为1.398,与患者性别无关(χ^2=0.08,P=0.778)。结论MICA*A5.1基因与乙肝后LC发病正相关,提示该基因可能是乙肝后出现LC的重要易感基因。Objective To study MICA gene polymorphism and the correlation of sMICA with HBsAg positive liver cirrhosis (LC). Methods MICA-STR mierosatellite genotyping was used to characterize the polymorphism of MICA exon 5 in 101 patients with HBsAg positive LC and 141 normal controls, and the relevance index between them was calculated. Results 5 kinds allelic gene and their frequencies were identified in MICA exon 5 and showed as below: MICA * A4 ( 10.9% ), MICA * A5 (37.1%), MICA * A5.1 (34.2%), MICA * A6 (7.4%), MICA * A9 ( 10.4% ). 15 genotypes including MICA * A4/A4, MICA * A4/A5, MICA A4/A5.1, MICA * A4/A6, MICA * A4/A9, MICA * A5/A5, MICA * A5/A5.1, MICA * A5/A6, MICA * A5/ A9, MICA * A5. 1/A5.1, MICA * A5. 1/A6, MICA * A5.1/A9, MICA * A6/A6, MICA * A6/A9, MICA * A9/ A9. Only MICA * A5.1 was positively associated with LC onset (P= 0.042), OR was 1.398, but was not associated with gender (χ^2= 0.08,P= 0.778). Conclusion MICA * A5.1 gene may be an important susceptibility gene leading to LC after infected with hepatitis B according to the positive correlation between MICA * A5.1 and hepatitis B induced LC.

关 键 词:MICA基因 可溶性MICA 肝硬化 乙型肝炎病毒 

分 类 号:R392.2[医药卫生—免疫学]

 

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