期刊文献+

乙肝患者MBL EXON I 54位基因频率检测

The Study on MBL EXON I 54 Gene Frequency in Hepatitis B Virus Infection
下载PDF
导出
摘要 目的:检测健康人及慢性乙肝患者MBL基因Exon I 54位密码子点突变的情况。方法:对MBL 54位密码子基因突变采用PCR-RLFP检测法。结果:检测64例健康汉族人54位密码子的点突变情况,野生型(GGC/GGC)为44例,占68.8%;突变杂合型(GGC/GAC)为19例,占29.6%,突变纯合子型(GAC/GAC)为1例,占1.6%,基因频率分别为GGC为0.836;GAC为0.164。检测54例乙肝患者,野生型为21例,占38.89%;突变杂合型为32例,占59.26%,突变纯合子型为1例,占1.85%,基因频率分别为GGC为0.6852;GAC为0.3148,健康人及慢性乙肝患者MBL基因54位密码子点突变有显著性差异,χ2=10.681P=0.005(按基因型统计);χ2=6.258P=0.012(按基因统计)。结论:乙肝患者组较健康对照组MBL基因Exon I 54位密码子点突变频率显著升高,提示该项指标在乙肝发生机理中的作用应进一步研究。 Objective: To analyze the genotypes of MBL Exon I 54 in the healthy and patients with HBV infection. Methods: The situations of PCR-RFLP method was used to describe and detect genotypes of MBL Exon I 54. Results:The situations of genotypes of MBL Exon I 54 in 64 healthy cases were that 44 people (68. 8%)were wildtype, 19 people(29.6%)were heterozygous(wildtype and mutant)1 people was mutant occupying 1.6 %, the genotypes of GGC and GAC were 0. 836 and 0. 164 respectively. The situations of genotypes of MBL in 54 HBV infections were that 21 people(38.89%) ,32 people(59.26%)were heterozygous(wild-type and mutant), 1 peoplewas mutant(1.85%) ,the genotype of GGC and GAC were 0. 6852 and 0. 3148. there was statistical significance between HBV infections and healthy(x^2= 10. 681 ,P=0. 005(genotype),x^2 =6. 258 P= 0. 012(gene)). Conclusion:The results show th.at MBL genotypes influence recovery from hepatitis B virus infection and need to study deeply.
出处 《河北北方学院学报(医学版)》 2008年第1期14-16,共3页 Journal of Hebei North University:Medical Edition
关键词 甘露糖结合凝集素 聚合酶链反应 肝炎病毒/乙型 基因型 Mannose-binding lectins PCR Hepatitis virus B Genotype
  • 相关文献

参考文献6

二级参考文献26

  • 1赵铁军,贾天军,程建君,刘华.检测MBL EXON Ⅰ 52位密码子突变PCR-SSP方法的建立[J].国际检验医学杂志,2004,26(5):396-398. 被引量:6
  • 2贾天军 刘士先.人甘露聚糖结合蛋白的提取及检测方法[J].中华现代实用医学杂志,1999,2(3):83-83.
  • 3Lau YL,Chan SY, Turner MW, et al. Mannosc--binding protein in preterm infants: decvelopment peofile and clinical significance. Clin Exp Immunol,1995,102:649-654
  • 4Peterslund NA, Koch C, Jensenius JC, et al. Association between deficiency of mannose-binding lectin and severe infections after chemotherapy. Lance,2001,358(9282) :637-638.
  • 5Neth O,Hann I,Turner MW,et al.Deficiency of mannose-binding lectin and burden of infection in children with malignancy:a prospective study.Lancet,2001,25(358):614-618
  • 6Kilpatrick DC. Mannan-binding lectin: clinical significance and applications. Biochim Biophys Acta,2002,1572(2-3):401-413
  • 7Sasaki K, Tsutsumi A,Wakamiya N,et al. Mannese-blnding lectln polymorphism in patients with hepatitisC vires infection .Scand J Gastroenterol,2000,9:960-965.
  • 8Steffensen R, Thiel S, Vanning K ,et al.Detection of structural and promoter polymorphism in the mannan-binding lectin(MBL) gene by polymerase chain reaction with sequence- specific primer.J Immunol Method,2000,241:33-42.
  • 9Boldt ABW, Petzl-Erler M L. A new strategy for mannose-binding lectin gene haplotyping.Human Mutation, 2002,19: 296-306.
  • 10Kilpatrick DC. Mannan - binding lectin: clinical significance and applicatiors. Biochim Biophys Acta, 2002, 1572(2~ 3): 401

共引文献30

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