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GWAS Study

Human leukocyte antigen variants and risk of hepatocellular carcinoma modified by hepatitis C virus genotypes: A genome-wide association study.

Lee MH, Huang YH, Chen HY et al.

28921602 PubMed ID
GWAS Study Type
2349 Participants
41 Views
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

LM
Lee MH
HY
Huang YH
CH
Chen HY
KS
Khor SS
CY
Chang YH
LY
Lin YJ
JC
Jen CL
LS
Lu SN
YH
Yang HI
NN
Nishida N
SM
Sugiyama M
MM
Mizokami M
YY
Yuan Y
LG
L'Italien G
TK
Tokunaga K
CC
Chen CJ
Chapter II

Abstract

Summary of the research findings

We conducted a genome-wide association study to discover genetic variants associated with hepatitis C virus (HCV)-related hepatocellular carcinoma (HCC). We genotyped 502 HCC cases and 749 non-HCC controls using the Axiom-CHB genome-wide array. After identifying single-nucleotide polymorphism clusters located in the human leukocyte antigen (HLA) region which were potentially associated with HCC, HLA-DQB1 genotyping was performed to analyze 994 anti-HCV seropositives collected in the period 1991-2013 in a community-based cohort for evaluating long-term predictability of HLA variants for identifying the risk of HCC. Cox proportional hazards models were used to estimate the hazard ratios and 95% confidence intervals of HLA genotypes for determining the aforementioned HCC risk. Eight single-nucleotide polymorphisms in the proximity of HLA-DQB1 were associated with HCC (P < 8.7 × 10-8 ) in the genome-wide association study. Long-term follow-up showed a significant association with HLA-DQB1*03:01 and DQB1*06:02 (P < 0.05). The adjusted hazard ratios associated with HCC were 0.45 (0.30-0.68) and 2.11 (1.34-3.34) for DQB1*03:01 and DQB1*06:02, respectively. After stratification by HCV genotypes, DQB1*03:01 showed protective effects only in patients with HCV genotype 1, whereas DQB1*06:02 conferred risk of HCC only in patients with HCV non-1 genotypes. HLA imputation analyses revealed that HLA-DRB1*15:01, which is in linkage disequilibrium with DQB1*06:02, also increased the risk of HCC (odds ratio, 1.96; 95% confidence interval, 1.31-2.93). Haplotype analysis supported that DQB1*03:01 and DQB1*06:02 are primarily protective and susceptible variants, respectively. Conclusion: HLA-DQB1 was independently associated with HCC; HCV genotypes modified the effects of HLA-DQB1 on the risk of HCC. (Hepatology 2018;67:651-661).

502 Chinese ancestry cases, 749 Chinese ancestry controls

Chapter III

Study Statistics

Key metrics and study information

2349
Total Participants
GWAS
Study Type
Yes
Replicated
669 Chinese ancestry cases, 429 Chinese ancestry controls
Replication Participants
East Asian
Ancestry
Taiwan
Recruitment Country
Chapter IV

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