Evidence map›Paper›PMID 42741325›Full record

ArticleTobacco induced diseases2026

Shared genetic architecture of smoking dependence and Crohn's disease: A cross-trait analysis of GWAS summary statistics.

Aocheng Ji, Wenbin Xu, Hao Xiong, Huan Zhong, Chunyan Zeng

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Article in Tobacco induced diseases, 2026. 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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5 · Who and what money

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5 authors.

Aocheng JiDepartment of Gastroenterology, Jiangxi Province Hospital of Integrated Chinese and Western Medicine, Nanchang, China.
Wenbin XuDepartment of Gastroenterology, Jiangxi Province Hospital of Integrated Chinese and Western Medicine, Nanchang, China.
Hao XiongEye Hospital of China Academy of Chinese Medical Sciences, Beijing, China.
Huan ZhongDepartment of Biochemistry and Molecular Biology, University of British Columbia, Vancouver, Canada.
Chunyan ZengDepartment of Gastroenterology, Jiangxi Province Hospital of Integrated Chinese and Western Medicine, Nanchang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSmoking dependence (SD) and Crohn's disease (CD) are epidemiologically associated, but whether this relationship reflects shared genetic susceptibility remains unclear.

methodsWe conducted a cross-trait genetic analysis of SD and CD using publicly available genome-wide association study (GWAS) summary statistics from European-ancestry populations. Genome-wide genetic correlation was estimated using linkage disequilibrium score regression (LDSC) and high-definition likelihood (HDL). Pleiotropic variants were identified using PLACO and mapped to genomic loci using FUMA. Regional signal sharing was assessed by Bayesian colocalization. Functional analyses included stratified LDSC, Multi-marker Analysis of GenoMic Annotation (MAGMA), GTEx tissue analysis, and Metascape. Expression-linked candidate genes were prioritized using expression quantitative trait locus (eQTL)-based summary-data-based Mendelian randomization (SMR) with heterogeneity in dependent instruments (HEIDI) testing. Genetically informed spatial mapping of cells for complex traits (gsMap) was used for spatial mapping.

resultsSD and CD showed positive genetic correlation by LDSC (rg=0.2090, p=0.0008) and HDL (rg=0.3817, p=0.00106). PLACO identified 81 genome-wide significant pleiotropic SNPs, which were mapped by FUMA to three loci at 1p31.3, 5p13.1, and 12q12, represented by rs11209031, rs1395152, and rs17467116, respectively. MAGMA identified 22 FDR-significant genes, four of which remained Bonferroni significant:

conclusionsSD and CD showed measurable shared genetic susceptibility, with convergent evidence from pleiotropic loci, immune-inflammatory pathway enrichment, tissue-level associations, and spatial transcriptomic mapping.

Indexed as

Crohn's diseasegsMapPLACOsmoking dependence

Identifiers

PMID42741325
PMCPMC13573291

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