Evidence map›Paper›PMID 42553996›Full record

ArticleInternational journal of rheumatic diseases2026

Genetic Association Between BTN3A1 Polymorphisms and the Risk of Rheumatoid Arthritis in a Chinese Population.

Qingxue Shu, Anfang Huang, Chengsong He

Abstract read
In one paragraph

Article in International journal of rheumatic 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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1 · What the graph read from it

What it found

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2 · The registry

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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

3 authors.

Qingxue ShuDepartment of Rheumatology and Immunology, The Affiliated Hospital, Southwest Medical University, Luzhou, Sichuan, China.
Anfang HuangDepartment of Rheumatology and Immunology, The Affiliated Hospital, Southwest Medical University, Luzhou, Sichuan, China.ORCID https://orcid.org/0000-0002-3860-8383
Chengsong HeDepartment of Rheumatology and Immunology, The Affiliated Hospital, Southwest Medical University, Luzhou, Sichuan, China.ORCID https://orcid.org/0009-0004-9843-1454

Funding

Natural Science Foundation of Sichuan Province 2024NSFSC0615
6 · The paper itself

Abstract

objectivesBTN3A1 has been associated with systemic lupus erythematosus (SLE) and psoriasis; however, its relationship with rheumatoid arthritis (RA) risk, particularly regarding BTN3A1 polymorphisms and RA susceptibility remains unclear.

methodsA total of 390 age- and sex-matched participants, including RA patients and healthy controls, were enrolled. Demographic, laboratory, and clinical data were collected. Five BTN3A1 polymorphisms (rs1796520, rs3857550, rs3208733, rs6912853, rs10456045) were genotyped. Allele and genotype associations between the groups were analyzed, as well as their associations with clinical and laboratory features in RA patients.

resultsAmong RA patients, 79.74% were female and 20.26% were male; among controls, 84.36% were female and 15.64% were male. For rs3208733, the frequencies of the CC genotype and C allele differed significantly between RA patients and controls. For rs6912853, the frequency of the TC genotype differed significantly. For rs10456045, the frequencies of the GG, AG, and GG + AG genotypes differed significantly. Regarding clinical and laboratory associations: for rs1796520, antinuclear antibody (ANA)-positive patients showed higher frequencies of the CC + TC genotype and C allele; anti-Rib-positive patients showed a higher frequency of the C allele. RA patients carrying the CC + TC genotype had fewer swollen joints and higher levels of IL-12p70 and IFN-α than TT carriers. For rs6912853, CC + TC carriers had fewer tender joints and higher levels of C-reactive protein (CRP) and IFN-γ than TT carriers.

conclusionBTN3A1 gene polymorphisms are associated with RA risk, suggesting future therapeutic exploration of BTN3A1 in RA.

Indexed as

Antigens, CDArthritis, RheumatoidButyrophilinsEast Asian PeoplePolymorphism, Single NucleotideAdultCase-Control StudiesChinaFemaleGene FrequencyGenetic Association StudiesGenetic Predisposition to DiseaseHumansMaleMiddle AgedPhenotypeAntigens, CDBTN3A1 protein, humanButyrophilinsBTN3A1polymorphismrheumatoid arthritis

Identifiers

PMID42553996
PMCPMC13439328

What Socratic holds

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Registered trials

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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 Socratic graph.