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Lack of association between hepatitis B virus infection and polymorphism of mannose-binding lectin gene in Korean population.
DC Field | Value | Language |
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dc.contributor.author | Cheong, JY | - |
dc.contributor.author | Cho, SW | - |
dc.contributor.author | Lim, SK | - |
dc.contributor.author | Shin, DH | - |
dc.contributor.author | Yoon, SK | - |
dc.contributor.author | Lee, JE | - |
dc.contributor.author | Hahm, KB | - |
dc.contributor.author | Kim, JH | - |
dc.date.accessioned | 2011-06-20T05:45:52Z | - |
dc.date.available | 2011-06-20T05:45:52Z | - |
dc.date.issued | 2005 | - |
dc.identifier.issn | 1011-8934 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/2975 | - |
dc.description.abstract | Mannose-binding lectin (MBL) plays an important role in immune defense. This study was undertaken to investigate the association between hepatitis B virus infection and polymorphisms of MBL gene. We assessed the single nucleotide polymorphism at codon 54 in exon 1 of MBL in patients with hepatitis B virus infection and HBsAg negative controls in Korean population. A total of 498 enrolled subjects was classified into four groups. Group 1; Clearance, Group 2; Inactive healthy carrier, Group 3; Chronic hepatitis, Group 4; Liver cirrhosis. MBL gene polymorphisms at codon 54 led to three genotypes (G/G, G/A, A/A). When we divided subjects into clearance group (group 1) and persistence group (group 2-4), G/G genotype and A-allele carrier were observed in 55.6% and 44.4% in clearance group, 64.8% and 35.2% in persistence group (p=0.081), respectively. When hepatitis B virus persistent cases were divided into inactive healthy carrier (group 2) and disease progression group (group 3 and 4), MBL gene polymorphisms at codon 54 were not related to disease progression (p=0.166). MBL gene polymorphism at codon 54 was not associated with the clearance of hepatitis B virus infection nor progression of disease in chronic hepatitis B virus infection. | - |
dc.language.iso | en | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Alleles | - |
dc.subject.MESH | Codon | - |
dc.subject.MESH | Disease Progression | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Fibrosis | - |
dc.subject.MESH | Genotype | - |
dc.subject.MESH | Hepatitis | - |
dc.subject.MESH | Hepatitis B | - |
dc.subject.MESH | Hepatitis B virus | - |
dc.subject.MESH | Heterozygote | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Korea | - |
dc.subject.MESH | Lectins | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Mannose-Binding Lectin | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Polymorphism, Genetic | - |
dc.subject.MESH | Polymorphism, Single Nucleotide | - |
dc.title | Lack of association between hepatitis B virus infection and polymorphism of mannose-binding lectin gene in Korean population. | - |
dc.type | Article | - |
dc.identifier.pmid | 15716605 | - |
dc.identifier.url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2808578/ | - |
dc.contributor.affiliatedAuthor | 정, 재연 | - |
dc.contributor.affiliatedAuthor | 조, 성원 | - |
dc.contributor.affiliatedAuthor | 함, 기백 | - |
dc.contributor.affiliatedAuthor | 김, 진홍 | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.3346/jkms.2005.20.1.65 | - |
dc.citation.title | Journal of Korean medical science | - |
dc.citation.volume | 20 | - |
dc.citation.number | 1 | - |
dc.citation.date | 2005 | - |
dc.citation.startPage | 65 | - |
dc.citation.endPage | 69 | - |
dc.identifier.bibliographicCitation | Journal of Korean medical science, 20(1). : 65-69, 2005 | - |
dc.identifier.eissn | 1598-6357 | - |
dc.relation.journalid | J010118934 | - |
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