Genome-Wide Association Study for Chronic Hepatitis B Infection in the Thai Population.

Bibliographic Details
Title: Genome-Wide Association Study for Chronic Hepatitis B Infection in the Thai Population.
Authors: Ashouri, Saeideh, Khor, Seik-Soon, Hitomi, Yuki, Sawai, Hiromi, Nishida, Nao, Sugiyama, Masaya, Kawai, Yosuke, Posuwan, Nawarat, Tangkijvanich, Pisit, Komolmit, Piyawat, Tsuiji, Makoto, Shotelersuk, Vorasuk, Poovorawan, Yong, Mizokami, Masashi, Tokunaga, Katsushi
Source: Frontiers in Genetics; 6/13/2022, Vol. 13, p1-10, 10p
Subject Terms: CHRONIC hepatitis B, GENOME-wide association studies, GENETIC variation, SINGLE nucleotide polymorphisms, HEPATITIS B virus
Abstract: To identify novel host genetic variants that predispose to hepatitis B virus (HBV) persistence, we performed the first genome-wide association study in the Thai population involving 318 cases of chronic hepatitis B and 309 healthy controls after quality control measures. We detected the genome-wide significant association of the HLA class II region (HLA-DPA1/DPB1 , rs7770370, p -value = 7.71 × 10−10, OR = 0.49) with HBV chronicity. Subsequent HLA allele imputation revealed HLA-DPA1*01:03 (Pc = 1.21 × 10−6, OR = 0.53), HLA-DPB1*02:01 (Pc = 2.17 × 10−3, OR = 0.50), and HLA-DQB1*06:09 (Pc = 2.17 × 10−2, OR = 0.07) as protective alleles, and HLA-DPA1*02:02 (Pc = 6.32 × 10−5, OR = 1.63), HLA-DPB1*05:01 (Pc = 1.13 × 10−4, OR = 1.72), HLA-DPB1*13:01 (Pc = 4.68 × 10−2, OR = 1.60), and HLA-DQB1*03:03 (Pc = 1.11 × 10−3, OR = 1.84) as risk alleles for HBV persistence. We also detected suggestive associations in the PLSCR1 (rs35766154), PDLIM5 (rs62321986), SGPL1 (rs144998273), and MGST1 (rs1828682) loci. Among single-nucleotide polymorphisms in the PLSCR1 locus, rs1061307 was identified as the primary functional variant by in silico/in vitro functional analysis. In addition to replicating the association of the HLA class II region, we detected novel candidate loci that provide new insights into the pathophysiology of chronic hepatitis B. [ABSTRACT FROM AUTHOR]
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Database: Complementary Index
More Details
ISSN:16648021
DOI:10.3389/fgene.2022.887121
Published in:Frontiers in Genetics
Language:English