期刊文献+

乙肝病毒A1762、G1764双突变是筛选男性HBsAg携带者肝癌最高危人群的生物学标记 被引量:5

HBV Core Promoter Double Mutations(A1762、G1764)Constitute a Valuable Biomarker to Identitya Subset of HBsAg Male Carriers at Extremely High Risk of Hepatocellular Carcinoma
下载PDF
导出
摘要 目的探讨乙肝病毒A1762、G1764双突变是否可作为筛选HBsAg携带者肝癌最高危人群的生物学标记。方法对2 258名乙肝病毒无症状携带者进行前瞻性队列研究,其中HBV A1762、G1764双突变株组1 261人,野毒株组997人,跟踪随访队列,每6个月1次对观察对象抽血进行甲胎蛋白(AFP)检测及B超体检以检查肝癌发病情况。结果观察48个月,2 258名乙肝病毒无症状携带者中,共发生肝癌72例,突变株组64例,野毒株组8例,发病率分别为932.2/10万人年和203.5/10万人年,两组发病率差异有统计学意义(P<0.001),相对危险度(RR)为4.58。突变株组男性发病率1 827.8/10万人年,明显高于野毒株组的180.5/10万人年,两者比较差异有统计学意义(P<0.001),相对危险度为10.13。92.5%的男性病例有双突变;突变株组女性发病率为686.6/10万人年,高于野毒株组的233.3/10万人年,两组比较差异有统计学意义(P<0.05),但相对危险度仅为2.94。结论双突变是筛选男性HBsAg携带者中肝癌最高危人群的很好生物学标记,但对女性筛选肝癌高危人群的意义不如男性。 Objective To determine whether HBV core promoter double mutations(A1762,G1764) constitute a valuable biomarker to identity a subset of HBsAg carriers at extremely high risk of hepatocellular carcinoma(HCC). Methods A cohort of 2 258 HBsAg positive subjects was recruited, which consist of HBV A1762, G1764 mutant group (n = 1 261 )and wild type group (n = 997 ). The study subjects were followed up 6-monthly with a purpose to diagnose HCC by measurements of serum alpha-fetoprotein levels and uhrasonographic examinations. Results Seventy-two cases of HCC were diagnosed after 48 months of follow-up. There were 64 cases in the mutant group and 8 cases in the wild-type group,giving HCC rates of 932.2/100 000 versus 203.5/100 000 person-years, respectively, the difference was signifieant(P 〈 0. 001 ). The relative risk (RR) was 4.58. With further stratification according to gender, the incidence rates of male mutant group and male wild-type group were 1827.8/1(10 000 and 180. 5/100 000 person-years, respectively. The difference was also significant (P 〈0. 001 )and RR was 10. 13. Specially ,92.5% (49/53)of the male cases in the cohort were infected with the mutant type. The incidence rates of female mutant group and female wild-type group were 686.6/100 000 and 233.3/100 000 person-years respectlvely,the difference was significant (P 〈0. 05) ,RR was only 2.94. Conclusion The data suggested that the double mutations (A1762、G1764)may be a good biomarker to identify a subset of male HBsAg carriers at extremely high risk of HCC but the value is less in female.
出处 《广西医学》 CAS 2011年第2期129-132,共4页 Guangxi Medical Journal
基金 英国Wellcome基金会资助项目(072058/Z/03/Z)
关键词 乙型肝炎病毒 表面抗原无症状携带者 A1762、G1764双突变 生物学标记 Hepatitis B virus HBsAg asymptomatic carriers A1762, G1764 double mutations Biomarker
  • 相关文献

参考文献5

二级参考文献29

共引文献156

同被引文献39

  • 1周建良,吴诗品.拉米夫定治疗乙型肝炎病毒B、C基因型疗效比较[J].中华肝脏病杂志,2004,12(8):489-490. 被引量:25
  • 2无.慢性乙型肝炎防治指南[J].实用肝脏病杂志,2006,9(1):8-18. 被引量:825
  • 3Stephan Schaefer.Hepatitis B virus taxonomy and hepatitis B virus genotypes[J].World Journal of Gastroenterology,2007,13(1):14-21. 被引量:43
  • 4郭耿龙,徐启桓,陈禄彪,张卡.265例原发性肝癌患者的乙型肝炎病毒血清学标志物分析[J].新医学,2007,38(1):28-29. 被引量:12
  • 5Michaelis M,Kleinschmidt M C,Barth S.Anti-cancer effects of artesunate in a panel of chemoresistant neuroblastoma cell lines[J].Biochem Pharmacol,2010,79 (2):130-136.
  • 6Ribeiro I R,Olliaro P.Safety of artemisinin and its derivatives.A review of published and unpublished clinical trials[J].Med Trop,1998,58(3):50-53.
  • 7Efferth T,Sauerbrey A,Olbrich A,et al.Molecular modes of ac-tion of artesunate in tumor cell lines[J].Mol Pharmacol,2003,64 (2):382-394.
  • 8Johann-Liang R,Albrecht R.Safety evaluations of drugs containing artemisinin derivatives for the treatment of malaria[J].Clin Infect Dis,2003,36(12):1627-1628.
  • 9Rasheed S A,Efferth T,Asangani I A,et al.First evidence that the antimalarial drug artesunate inhibits invasion and in vivo metastasis in lung cancer by targeting essential extracellular proteases[J].Int J Cancer,2010,127(6):1475-1485.
  • 10Youns M,Hoheisel J D,Efferth T.Traditional Chinese medicines (TCMs) for molecular targeted therapies of tumours[J].Curr Drug Discov Technol,2010,7(1):37-45.

引证文献5

二级引证文献15

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部