中华肝脏病杂志
中華肝髒病雜誌
중화간장병잡지
CHINESE JOURNAL OF HEPATOLOGY
2008年
8期
586-589
,共4页
房婕%LIU Zheng-wen%韩群英%LOU Sai%陈静宏
房婕%LIU Zheng-wen%韓群英%LOU Sai%陳靜宏
방첩%LIU Zheng-wen%한군영%LOU Sai%진정굉
肝炎病毒,丙型%转化生长因子β%多态性,单核苷酸
肝炎病毒,丙型%轉化生長因子β%多態性,單覈苷痠
간염병독,병형%전화생장인자β%다태성,단핵감산
Hepatitis C virus%Transforming growth factor beta%Polymorphisrn,single nucleotide
目的 探讨HCV感染者转化生长因子β1(TGF β1)信号肽区密码子25基因多态性与HCV感染的相关性. 方法 采用扩增阻碍突变系统方法,分析106名健康对照者和85例慢性HCV感染者的TGF β1信号肽区密码子25基因多态性. 结果 TGF β1信号肽区密码子25的基因型分布与基因频数在HCV感染组和对照组之间,慢性丙型肝炎组和HCV相关肝硬化组之间的差异均无统计学意义.密码子25基因型分布在ALT正常组和ALT升高组之间的差异无统计学意义,但G基因频数在ALT升高组(G=108)较ALT正常组(G=47)高(P-0.040).密码子25基因型分布在尢病毒血症组(GG=18,CG=5,CC=3)和病毒血症组(GG=55,CG=4)之间的差异有统计学意义(P=0.005),且G等位基因更多出现干病毒血症组(P=0.000).结论 TGF β1信号肽区密码子25G→C突变影响HCV感染肝脏炎性反应,G等位基因与HCV感染病毒血症相关,TGF β1信号肽区密码子25G→C突变可能是影响HCV感染结局的因素之一.
目的 探討HCV感染者轉化生長因子β1(TGF β1)信號肽區密碼子25基因多態性與HCV感染的相關性. 方法 採用擴增阻礙突變繫統方法,分析106名健康對照者和85例慢性HCV感染者的TGF β1信號肽區密碼子25基因多態性. 結果 TGF β1信號肽區密碼子25的基因型分佈與基因頻數在HCV感染組和對照組之間,慢性丙型肝炎組和HCV相關肝硬化組之間的差異均無統計學意義.密碼子25基因型分佈在ALT正常組和ALT升高組之間的差異無統計學意義,但G基因頻數在ALT升高組(G=108)較ALT正常組(G=47)高(P-0.040).密碼子25基因型分佈在尢病毒血癥組(GG=18,CG=5,CC=3)和病毒血癥組(GG=55,CG=4)之間的差異有統計學意義(P=0.005),且G等位基因更多齣現榦病毒血癥組(P=0.000).結論 TGF β1信號肽區密碼子25G→C突變影響HCV感染肝髒炎性反應,G等位基因與HCV感染病毒血癥相關,TGF β1信號肽區密碼子25G→C突變可能是影響HCV感染結跼的因素之一.
목적 탐토HCV감염자전화생장인자β1(TGF β1)신호태구밀마자25기인다태성여HCV감염적상관성. 방법 채용확증조애돌변계통방법,분석106명건강대조자화85례만성HCV감염자적TGF β1신호태구밀마자25기인다태성. 결과 TGF β1신호태구밀마자25적기인형분포여기인빈수재HCV감염조화대조조지간,만성병형간염조화HCV상관간경화조지간적차이균무통계학의의.밀마자25기인형분포재ALT정상조화ALT승고조지간적차이무통계학의의,단G기인빈수재ALT승고조(G=108)교ALT정상조(G=47)고(P-0.040).밀마자25기인형분포재왕병독혈증조(GG=18,CG=5,CC=3)화병독혈증조(GG=55,CG=4)지간적차이유통계학의의(P=0.005),차G등위기인경다출현간병독혈증조(P=0.000).결론 TGF β1신호태구밀마자25G→C돌변영향HCV감염간장염성반응,G등위기인여HCV감염병독혈증상관,TGF β1신호태구밀마자25G→C돌변가능시영향HCV감염결국적인소지일.
Objective To investigate the possible relationship between polymorphism of codon25 in signal peptide region of transforming growth factor beta 1 (TGF β1) and hepatitis C virus (HCV) infection susceptibility. Methods Genotypes ofTGF β1 of 191 subjects (85 HCV infected patients and 106 healthycontrols) were studied. Genotypes of TGF β1 codon25 were determined by amplification refractory mutation system (ARMS). Results Differences of codon25 polymorphism were not found between HCV infected patients and the controls (P>0.05), which showed a similar pattern between the chronic hepatitis C group and HCV-associated liver cirrhosis group (P>0.05). There were no differences of genotype distribution of codon25 between ALT normal and ALT elevated patients (P>0.05), but G allele frequency was higher in ALT elevated group (P=0.040). There were great differences between the distribution of genotypes (P=0.005) and allele frequency (P=0.000) of the HCV RNA positive and the negative groups in that the HCV RNA positive group differed greatly from the negative group. Conclusion Polymorphism of TGF β1 codon25 may influence the grade of liver inflammatory activity. High G allele frequency of codon25 may be associated with viremia in patients with chronic HCV infection. It seems that polymorphism of codon25 in the signal peptide region of TGF β1 may contribute to the outcome of HCV infected patients.