Evidence map›Paper›PMID 40340985›Full record

ArticleJournal of the Chinese Medical Association : JCMA2025

Association of PBRM1 rs2251219 with major depressive disorder and biochemical variables in a Taiwanese cohort.

Kuan-Ju Chou, Chuan-Hsun Yu, Yu-Ting Yan, Po-Hsiu Kuo, Shih-Jen Tsai

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Article in Journal of the Chinese Medical Association : JCMA, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Effect ofBJPsych open · 2026
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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Kuan-Ju ChouDepartment of General Psychiatry, Yu Li Hospital, Ministry of Health and Welfare, Hualien, Taiwan, ROC.
Chuan-Hsun YuDepartment of General Psychiatry, Yu Li Hospital, Ministry of Health and Welfare, Hualien, Taiwan, ROC.
Yu-Ting YanDepartment of Public Health & Institute of Epidemiology and Preventive Medicine, National Taiwan University, Taipei, Taiwan, ROC.
Po-Hsiu KuoDepartment of Public Health & Institute of Epidemiology and Preventive Medicine, National Taiwan University, Taipei, Taiwan, ROC.
Shih-Jen TsaiDepartment of Psychiatry, National Taiwan University Hospital, Taipei, Taiwan, ROC.ORCID 0000-0002-9987-022

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGenetic studies have identified more than 100 loci linked to major depressive disorder (MDD), underscoring its polygenic characteristics. Although the protein polybromo-1 ( PBRM1 ) rs2251219 polymorphism was reported to be associated with MDD, this has not been corroborated by additional studies. In the present study, the associations between PBRM1 rs2251219, MDD, and key biochemical variables were evaluated in a large Taiwanese cohort.

methodsData were collected from 117 679 individuals aged 30 to 90 years who were enrolled in the Taiwan Biobank. MDD diagnoses were based on self-reported data validated through national insurance claims records. Genotyping was conducted with an Axiom Genome-Wide Array, and associations with biochemical variables were analyzed through a general linear model adjusted for age and sex.

resultsA significant association was observed between PBRM1 rs2251219 and MDD risk ( p = 0.021 for genotype and p = 0.025 for allele). Individuals with the T allele had a higher MDD risk than C/C genotype carriers did. Biochemical differences were also observed, with T/T carriers with lower body mass index, platelet counts, albumin concentrations, and fasting glucose levels and higher red blood cell counts, hematocrit levels, and uric acid levels.

conclusionThe PBRM1 rs2251219 polymorphism was associated with both MDD and biochemical measurement variation. These findings support the effects of the PBRM1 rs2251219 polymorphism on blood protein levels and psychiatric traits.

Indexed as

Major Depressive DisorderNuclear ProteinsPolymorphism, Single NucleotideAdultAgedAged, 80 and overCohort StudiesFemaleGenotypeHumansMaleMiddle AgedTaiwanNuclear ProteinsAssociation studyBiochemical variablesMajor depressive disorderTaiwan Biobank

Identifiers

PMID40340985
PMCPMC12637117

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