Up Regulation of ZNF76 rs10947540 and SCUBE3 rs1888822 Single Nucleotide Polymorphisms as a Genetic Risk Factor in Egyptian Patients with Rheumatoid Arthritis.

IF 2.9 4区 医学 Q3 IMMUNOLOGY
Immunological Investigations Pub Date : 2025-01-01 Epub Date: 2024-12-19 DOI:10.1080/08820139.2024.2418569
Eman Abd Allah Fouda, Alshimaa Mohamed Elmalawany, Eman Masoud Abd El Gayed, Salah Mohamed El-Kousy, Heba Saber Mohamed, Ahmed B Zaid, Mohamed Farag Ali Assar
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引用次数: 0

Abstract

Introduction: The protein SCUBE3 has been observed to exhibit an association with various autoimmune conditions, including psoriasis and rheumatoid arthritis. Genetic experiments have revealed that changes in Zinc finger protein-coding sequences correlate with an increased vulnerability to developing autoimmune diseases, so we aimed to study investigates the involvement of ZNF76 rs10947540 and SCUBE3 rs1888822 gene expression in individuals diagnosed with Rheumatoid Arthritis.

Methods: In a case-control study conducted from January 2022 to March 2023, 80 adults with RA from Menoufia University Hospital were compared with 80 age- and gender-matched healthy controls. Single nucleotide polymorphisms (SNPs) ZNF76 rs10947540 and SCUBE3 rs1888822 were analysed using real-time polymerase chain reaction (PCR).

Results: ZNF76 rs10947540 demonstrated a 7.125-fold increased risk for RA in CC genotype individuals and a 2.958-fold risk associated with the C allele. Those with the TC genotype had a 2.523-fold increased risk. Similarly, SCUBE3 rs1888822 showed a 6.364-fold risk for RA in TT genotype individuals and a 3.065-fold risk for T allele carriers. GT genotype individuals had a 2.765-fold risk.

Discussion: Our study suggests that ZNF76 rs10947540 and SCUBE3 rs1888822 polymorphisms may be risk factors for RA in Egyptian patients. Understanding the genetic variations associated with higher risk underscores the role of genetics in RA progression.

ZNF76 rs10947540和SCUBE3 rs1888822单核苷酸多态性上调在埃及类风湿关节炎患者中的遗传风险因素
导读:已经观察到蛋白SCUBE3与多种自身免疫性疾病(包括牛皮癣和类风湿性关节炎)相关。遗传实验显示锌指蛋白编码序列的变化与自身免疫性疾病易感性增加相关,因此我们旨在研究ZNF76 rs10947540和SCUBE3 rs1888822基因表达在类风湿关节炎患者中的作用。方法:在2022年1月至2023年3月进行的一项病例对照研究中,将来自Menoufia大学医院的80名成人RA患者与80名年龄和性别匹配的健康对照组进行比较。采用实时聚合酶链反应(PCR)对ZNF76 rs10947540和SCUBE3 rs1888822的单核苷酸多态性(snp)进行分析。结果:ZNF76 rs10947540显示,CC基因型个体患RA的风险增加7.125倍,与C等位基因相关的风险增加2.958倍。TC基因型患者的风险增加了2.523倍。同样,scucbe3 rs1888822在TT基因型个体中显示出6.364倍的RA风险,在T等位基因携带者中显示出3.065倍的风险。GT基因型个体的风险为2.765倍。讨论:我们的研究提示ZNF76 rs10947540和SCUBE3 rs1888822多态性可能是埃及RA患者的危险因素。了解与高风险相关的遗传变异强调了遗传在类风湿关节炎进展中的作用。
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来源期刊
Immunological Investigations
Immunological Investigations 医学-免疫学
CiteScore
5.50
自引率
7.10%
发文量
49
审稿时长
3 months
期刊介绍: Disseminating immunological developments on a worldwide basis, Immunological Investigations encompasses all facets of fundamental and applied immunology, including immunohematology and the study of allergies. This journal provides information presented in the form of original research articles and book reviews, giving a truly in-depth examination of the latest advances in molecular and cellular immunology.
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