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Association of polymorphism in MicroRNA 219-1 with clearance of hepatitis B virus infection.
DC Field | Value | Language |
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dc.contributor.author | Cheong, JY | - |
dc.contributor.author | Shin, HD | - |
dc.contributor.author | Kim, YJ | - |
dc.contributor.author | Cho, SW | - |
dc.date.accessioned | 2014-05-15 | - |
dc.date.available | 2014-05-15 | - |
dc.date.issued | 2013 | - |
dc.identifier.issn | 0146-6615 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/9958 | - |
dc.description.abstract | Polymorphisms in the primary microRNA region may be associated with natural course of hepatitis B virus (HBV) infection. This study evaluated if the mircoRNA 219-1 (miR-219-1) polymorphism can influence the susceptibility towards persistence of HBV infection and the progression to hepatocellular carcinoma (HCC) in patients with chronic HBV infection. A total of 1,439 individuals having either past or present evidence of HBV infection were enrolled for the study. The subjects were divided into four groups; (1) spontaneous recovery (n = 404), (2) chronic HBV carrier (n = 313), (3) chronic HBV carrier with cirrhosis (n = 305), and (4) hepatocellular carcinoma (n = 417). Genotyping was performed at three polymorphic variants (rs421446, rs107822, and rs213210) in the pri-miRNA region of miR-219-1. The rs421446 T allele was found to be strongly associated with HBV clearance (OR = 0.73, P = 0.0005 in a codominant model and OR = 0.67, P = 0.0009 in a dominant model, OR = 0.69, P = 0.04 in a recessive model, respectively). The rs107822 G allele was also found to be associated with HBV clearance (OR = 0.79, P = 0.008 in a codominant model and OR = 0.72, P = 0.01 in a dominant model, respectively). In haplotype analysis, ht2 (T-G-T) and ht1 (C-A-C) were found to be in significant association with the clearance of HBV. However, no significant association was observed between miR-219-1 polymorphism and the risk of HCC occurrence. This result suggests that polymorphisms in the pri-miRNA region of miR-219-1 might be a genetic factor for HBV clearance after infection. | - |
dc.format | application/pdf | - |
dc.language.iso | en | - |
dc.subject.MESH | Adolescent | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Aged | - |
dc.subject.MESH | Aged, 80 and over | - |
dc.subject.MESH | Carcinoma, Hepatocellular | - |
dc.subject.MESH | Carrier State | - |
dc.subject.MESH | Case-Control Studies | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Hepatitis B | - |
dc.subject.MESH | Hepatitis B virus | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Liver Cirrhosis | - |
dc.subject.MESH | Liver Neoplasms | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | MicroRNAs | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Polymorphism, Genetic | - |
dc.subject.MESH | Young Adult | - |
dc.title | Association of polymorphism in MicroRNA 219-1 with clearance of hepatitis B virus infection. | - |
dc.type | Article | - |
dc.identifier.pmid | 23508906 | - |
dc.contributor.affiliatedAuthor | 정, 재연 | - |
dc.contributor.affiliatedAuthor | 조, 성원 | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.1002/jmv.23551 | - |
dc.citation.title | Journal of medical virology | - |
dc.citation.volume | 85 | - |
dc.citation.number | 5 | - |
dc.citation.date | 2013 | - |
dc.citation.startPage | 808 | - |
dc.citation.endPage | 814 | - |
dc.identifier.bibliographicCitation | Journal of medical virology, 85(5). : 808-814, 2013 | - |
dc.identifier.eissn | 1096-9071 | - |
dc.relation.journalid | J001466615 | - |
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