Lin Li, Jiankang Shan, Haixin Fang, Guangqi An, Min Zhang, Pengyi Zhou, Kunpeng Xie, Bo Jin, Haiyan Zhu, Xuemin Jin, Peizeng Yang, Liping Du
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The results revealed no statistically significant correlation between the two specified single-nucleotide polymorphisms of <i>TBX21</i> (rs11657479 C/T and rs4794067 C/T) and susceptibility to AS. However, upon conducting stratification analysis, our findings demonstrated a significant association between rs11657479 and susceptibility to human leucocyte antigen (HLA)-B27<sup>+</sup> AS in allelic (C vs. T: odds ratio [OR] = 1.52, 95%CI = 1.09–2.11, corrected <i>p</i> [pc] = .028), heterozygous (CT vs. TT: OR = 1.63, 95%CI = 1.13–2.34, pc = .016) and dominant (CT + CC vs. TT: OR = 1.60, 95%CI = 1.12–2.28, pc = .018) models. Furthermore, the haplotype rs4794067/C-rs11657479/C of <i>TBX21</i> was found to increase the risk of HLA-B27<sup>+</sup> AS cases. In conclusion, our findings indicate a correlation between <i>TBX21</i> gene polymorphism and HLA-B27<sup>+</sup> AS patients within the Chinese population.</p>","PeriodicalId":14003,"journal":{"name":"International Journal of Immunogenetics","volume":"51 3","pages":"143-148"},"PeriodicalIF":2.3000,"publicationDate":"2024-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Correlation of TBX21 gene polymorphisms with ankylosing spondylitis in a Chinese population\",\"authors\":\"Lin Li, Jiankang Shan, Haixin Fang, Guangqi An, Min Zhang, Pengyi Zhou, Kunpeng Xie, Bo Jin, Haiyan Zhu, Xuemin Jin, Peizeng Yang, Liping Du\",\"doi\":\"10.1111/iji.12659\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Genome-wide association studies analysis has revealed associations between ankylosing spondylitis (AS) and loci on the <i>TBX21</i> gene across various populations. 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引用次数: 0
摘要
全基因组关联研究分析表明,在不同人群中,强直性脊柱炎(AS)与TBX21基因上的位点存在关联。本研究旨在探讨中国人群强直性脊柱炎发病风险较高与 TBX21 基因的两个多态性位点之间是否存在关联。为此,我们对363名强直性脊柱炎患者和907名健康人进行了病例对照调查。基因分型采用 iPLEX Gold 基因分型测定法进行。使用 SPSS 23.0 和 SHEsis 软件对基因型和单倍型进行了分析。结果显示,TBX21的两个特定单核苷酸多态性(rs11657479 C/T和rs4794067 C/T)与强直性脊柱炎易感性之间没有统计学意义上的显著相关性。然而,在进行分层分析后,我们的研究结果表明,rs11657479 与等位基因(C vs. T:几率比[OR] = 0.5)中人类白细胞抗原(HLA)-B27+ AS 的易感性有显著关联。T:比值比 [OR] = 1.52,95%CI = 1.09-2.11,校正 p [pc] = .028)、杂合子(CT vs. TT:OR = 1.63,95%CI = 1.13-2.34,pc = .016)和显性(CT + CC vs. TT:OR = 1.60,95%CI = 1.12-2.28,pc = .018)模型。此外,还发现 TBX21 的单倍型 rs4794067/C-rs11657479/C 增加了 HLA-B27+ AS 病例的风险。总之,我们的研究结果表明,在中国人群中,TBX21 基因多态性与 HLA-B27+ AS 患者之间存在相关性。
Correlation of TBX21 gene polymorphisms with ankylosing spondylitis in a Chinese population
Genome-wide association studies analysis has revealed associations between ankylosing spondylitis (AS) and loci on the TBX21 gene across various populations. This study aimed to investigate if there is a connection between a higher risk of AS in a Chinese population and two polymorphism loci on the TBX21 gene. To achieve this, we performed a case–control investigation involving 363 patients with AS and 907 healthy individuals. Genotyping was carried out using the iPLEX Gold genotyping assay. The analysis of genotypes and haplotypes was performed using SPSS 23.0 and SHEsis software. The results revealed no statistically significant correlation between the two specified single-nucleotide polymorphisms of TBX21 (rs11657479 C/T and rs4794067 C/T) and susceptibility to AS. However, upon conducting stratification analysis, our findings demonstrated a significant association between rs11657479 and susceptibility to human leucocyte antigen (HLA)-B27+ AS in allelic (C vs. T: odds ratio [OR] = 1.52, 95%CI = 1.09–2.11, corrected p [pc] = .028), heterozygous (CT vs. TT: OR = 1.63, 95%CI = 1.13–2.34, pc = .016) and dominant (CT + CC vs. TT: OR = 1.60, 95%CI = 1.12–2.28, pc = .018) models. Furthermore, the haplotype rs4794067/C-rs11657479/C of TBX21 was found to increase the risk of HLA-B27+ AS cases. In conclusion, our findings indicate a correlation between TBX21 gene polymorphism and HLA-B27+ AS patients within the Chinese population.
期刊介绍:
The International Journal of Immunogenetics (formerly European Journal of Immunogenetics) publishes original contributions on the genetic control of components of the immune system and their interactions in both humans and experimental animals. The term ''genetic'' is taken in its broadest sense to include studies at the evolutionary, molecular, chromosomal functional and population levels in both health and disease. Examples are:
-studies of blood groups and other surface antigens-
cell interactions and immune response-
receptors, antibodies, complement components and cytokines-
polymorphism-
evolution of the organisation, control and function of immune system components-
anthropology and disease associations-
the genetics of immune-related disease: allergy, autoimmunity, immunodeficiency and other immune pathologies-
All papers are seen by at least two independent referees and only papers of the highest quality are accepted.