Evidence map›Paper›PMID 42622066›Full record

ArticlePediatrics international : official journal of the Japan Pediatric Society

Loci Associated With Susceptibility to Biliary Atresia-A Genome-Wide Association Study in Taiwan.

Chieh-Yu Chu, Chi-San Tai, Chien-Ting Hsu, Kai-Chi Chang, Huey-Ling Chen, Yen-Hsuan Ni, Mei-Hwei Chang, Jia-Feng Wu

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Article in Pediatrics international : official journal of the Japan Pediatric Society. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Chieh-Yu ChuDepartment of Pediatrics, National Taiwan University Hospital Yunlin Branch, Douliu City, Taiwan.
Chi-San TaiDepartment of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan.
Chien-Ting HsuDepartment of Pediatrics, National Taiwan University Hospital Hsinchu Branch, Hsinchu, Taiwan.
Kai-Chi ChangDepartment of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan.ORCID https://orcid.org/0000-0002-9720-3810
Huey-Ling ChenDepartment of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan.ORCID https://orcid.org/0000-0002-4074-5838
Yen-Hsuan NiDepartment of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan.ORCID https://orcid.org/0000-0002-1158-5249
Mei-Hwei ChangDepartment of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan.ORCID https://orcid.org/0000-0002-3648-9261
Jia-Feng WuDepartment of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan.ORCID https://orcid.org/0000-0001-6343-1658

Funding

National Taiwan University Hospital NTUH.110-T05National Taiwan University Hospital NTUH.111-T0009National Taiwan University Hospital NTUH. 112-E0009
6 · The paper itself

Abstract

backgroundBiliary atresia (BA) is the leading cause of pediatric liver transplantation worldwide. However, the genetic background remains unclear in most patients. In this genome-wide association study (GWAS), we aimed to identify genetic loci that contribute to susceptibility to BA.

methodsWe recruited 189 BA patients (85 males and 104 females) and 558 non-BA controls (275 males and 283 females) for this GWAS analysis using the Axiom Genome-Wide TWB 2.0 Array with 686,463 single-nucleotide polymorphisms (SNPs). The MassARRAY Sequenom analysis was then applied to validate the identified top SNPs.

resultsWe identified rs139120621 (odds ratio [OR] = 17.31, p = 2.78 × 10

conclusionsWe identified novel loci of BA susceptibility SNPs in a Taiwanese cohort by the GWAS analysis. These findings shed light on the genetic factors in the pathophysiology of BA that might be applied to the future development of therapeutic agents for BA patients.

Indexed as

Biliary AtresiaGenetic Predisposition to DiseaseGenome-Wide Association StudyFemaleHumansInfantMalePolymorphism, Single NucleotideTaiwanbiliary atresiagenome‐wide association studyplatelet‐derived growth factor Csingle‐nucleotide polymorphism

Identifiers

PMID42622066
PMCPMC13491567

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.