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No association for Chinese HBV-related hepatocellular carcinoma susceptibility SNP in other East Asian populations.

Title
 No association for Chinese HBV-related hepatocellular carcinoma susceptibility SNP in other East Asian populations.
Authors
 Hiromi Sawai; Nao Nishida; Katsushi Tokunaga; Masashi Mizokami; Yasuhito Tanaka; Yusuke Nakamura; Man-Fung Yuen; Jun Yong Park; Kwang-Hyub Han; Sang Hoon Ahn; Masaya Sugiyama; Kiyoaki Ito; Tatsuya Ide; Yoichi Hiasa; Yoshikazu Murawaki; Keisuke Hino; Masaaki Korenaga; Eiji Mita; Yoshito Itoh; Kentaro Matsuura; Eiji Tanaka; Shuichi Kaneko; Masao Honda; Namiki Izumi; Yasuhiro Asahina; Masayuki Kurosaki; Masaaki Watanabe; Satoshi Mochida; Koichi Abe; Jong-Hon Kang; Shuhei Hige; Megumi Yamaoka; Yoriko Mawatari; Koichi Matsuda; Hamdi Mbarek
Issue Date
2012
Journal Title
 BMC Medical Genetics
ISSN
 1471-2350
Citation
 BMC Medical Genetics, Vol.13(null) : 47, 2012
Abstract
BACKGROUND: A recent genome-wide association study (GWAS) using chronic HBV (hepatitis B virus) carriers with and without hepatocellular carcinoma (HCC) in five independent Chinese populations found that one SNP (rs17401966) in KIF1B was associated with susceptibility to HCC. In the present study, a total of 580 HBV-derived HCC cases and 1351 individuals with chronic hepatitis B (CHB) or asymptomatic carrier (ASC) were used for replication studies in order to evaluate the reported association with HBV-derived HCC in other East Asian populations. RESULTS: We did not detect any associations between rs17401966 and HCC in the Japanese cohorts (replication 1: OR = 1.09, 95 % CI = 0.82-1.43; replication 2: OR = 0.79, 95 % CI = 0.54-1.15), in the Korean cohort (replication 3: OR = 0.95, 95 % CI = 0.66-1.36), or in the Hong Kong Chinese cohort (replication 4: OR = 1.17, 95 % CI = 0.79-1.75). Meta-analysis using these cohorts also did not show any associations with P = 0.97. CONCLUSIONS: None of the replication cohorts showed associations between rs17401966 and HBV-derived HCC. This may be due to differences in the genetic diversity among the Japanese, Korean and Chinese populations. Other reasons could be the high complexity of multivariate interactions between the genomic information and the phenotype that is manifesting. A much wider range of investigations is needed in order to elucidate the differences in HCC susceptibility among these Asian populations.
URI
http://ir.ymlib.yonsei.ac.kr/handle/22282913/89788
DOI
10.1186/1471-2350-13-47
Appears in Collections:
1. 연구논문 > 1. College of Medicine > Dept. of Internal Medicine
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