Association of PTPN22 and NLRP3 Gene Polymorphisms with Psoriasis Susceptibility in a Han Chinese Population.

IF 1.2 4区 生物学 Q4 GENETICS & HEREDITY
Genetic testing and molecular biomarkers Pub Date : 2026-04-01 Epub Date: 2026-04-07 DOI:10.1177/19450265261440160
Jiajia Zhang, Wei Xia, Yafeng Tan, Liangliang Ouyang, Fusheng Xie, Tao Jiang
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引用次数: 0

Abstract

Objective: To investigate the associations among protein tyrosine phosphatase (PTPN22), nucleotide-binding oligomerization domain-like receptor protein 3 (NLRP3) and genetic susceptibility to psoriasis in the Jiujiang population.

Methods: A total of 120 psoriasis patients and 90 healthy controls were enrolled. Polymerase chain reaction-based sequencing was performed to determine the distribution of PTPN22 rs1310182, rs2488457, and NLRP3 rs10754558 genotypes. Logistic regression analysis was conducted to evaluate the associations between the genotypes, alleles, and genetic models of these three loci and psoriasis susceptibility. The associations between these polymorphisms and disease subtypes or severity were also explored.

Results: With respect to the PTPN22 rs2488457 locus, the GG genotype and G allele were identified as risk factors for psoriasis susceptibility (p = 0.026 and p = 0.004, respectively). In the dominant model, carriers of the GG genotype exhibited a significantly higher risk of psoriasis than did those with the GC+CC genotype (p = 0.016). No significant associations were observed between the rs1310182 or rs10754558 polymorphisms and psoriasis susceptibility (p > 0.05). In addition, none of the three loci were significantly correlated with the disease subtype or severity (p > 0.05).

Conclusions: In the Jiujiang population, the GG genotype and G allele of the PTPN22 rs2488457 locus may be key factors influencing psoriasis susceptibility.

PTPN22和NLRP3基因多态性与中国汉族银屑病易感性的关系
目的:探讨九江人群酪氨酸蛋白磷酸酶(PTPN22)、核苷酸结合寡聚结构域样受体蛋白3 (NLRP3)与银屑病遗传易感性的关系。方法:选取120例银屑病患者和90例健康对照者。采用基于聚合酶链反应的测序方法确定PTPN22 rs1310182、rs2488457和NLRP3 rs10754558基因型的分布。Logistic回归分析这三个位点的基因型、等位基因和遗传模型与银屑病易感性之间的关系。这些多态性与疾病亚型或严重程度之间的关系也被探讨。结果:PTPN22 rs2488457位点GG基因型和G等位基因是银屑病易感性的危险因素(p = 0.026和p = 0.004)。在优势模型中,GG基因型携带者患牛皮癣的风险明显高于GC+CC基因型携带者(p = 0.016)。rs1310182或rs10754558多态性与银屑病易感性之间无显著相关性(p < 0.05)。此外,三个基因座与疾病亚型或严重程度均无显著相关性(p < 0.05)。结论:在九江人群中,PTPN22 rs2488457位点GG基因型和G等位基因可能是影响银屑病易感性的关键因素。
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来源期刊
CiteScore
2.50
自引率
7.10%
发文量
63
审稿时长
1 months
期刊介绍: Genetic Testing and Molecular Biomarkers is the leading peer-reviewed journal covering all aspects of human genetic testing including molecular biomarkers. The Journal provides a forum for the development of new technology; the application of testing to decision making in an increasingly varied set of clinical situations; ethical, legal, social, and economic aspects of genetic testing; and issues concerning effective genetic counseling. This is the definitive resource for researchers, clinicians, and scientists who develop, perform, and interpret genetic tests and their results. Genetic Testing and Molecular Biomarkers coverage includes: -Diagnosis across the life span- Risk assessment- Carrier detection in individuals, couples, and populations- Novel methods and new instrumentation for genetic testing- Results of molecular, biochemical, and cytogenetic testing- Genetic counseling
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