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CFI-rs7356506 is a genetic protective factor for acute anterior uveitis in Chinese patients

机译:CFI-rs7356506是中国患者急性前葡萄膜炎的遗传保护因子

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Background: Complement Factor I (CFI ) and the CD46 complement regulator (CD46) play an important role in the complement activation pathways, which is known to affect the development of uveitis. The present study was performed to investigate the association of the CFI and CD46 genes with acute anterior uveitis (AAU). Methods: A total of 600 subjects (300 patients with AAU and 300 healthy controls) were recruited for this case-control study. Six CFI single nucleotide polymorphisms (SNP) (rs7356506, rs10029485, rs11726949, rs12512308, rs7438961, rs998538) and four CD46 SNPs (rs12138764, rs2466571, rs2796278, rs7545126) were genotyped using Sequenom MassARRAY technology. Allele and genotype frequencies were compared between patients and controls using the χ2 test. Analyses were stratified for gender, human leukocyte antigen (HLA)-B27, and ankylosing spondylitis status. Results: Rs7356506 in the CFI gene was found to be protective against AAU. There was a significant increase in the frequency of the A allele (p=0.003, pc=0.03, OR=0.684, CI 0.534 to 0.876) and AA homozygosity (p=0.004, pc=0.04, OR=0.624, CI 0.452 to 0.862) in AAU patients as compared to controls. Stratified analysis, according to gender and HLA-B27 status for AAU, also revealed the association with CFI-rs7356506. None of the tested SNPs of CD46 were associated with AAU. Conclusions: This study has revealed a significant association between AAU and CFI-rs7356506, suggesting that CFI is involved in the pathogenesis of AAU, and that its influence on AAU may differ depending on gender and HLA-B27 status.
机译:背景:补体因子I(CFI)和CD46补体调节剂(CD46)在补体激活途径中起着重要作用,已知该途径会影响葡萄膜炎的发展。本研究旨在研究CFI和CD46基因与急性前葡萄膜炎(AAU)的关联。方法:本研究共招募了600名受试者(300名AAU患者和300名健康对照)。使用Sequenom MassARRAY技术对六个CFI单核苷酸多态性(SNP)(rs7356506,rs10029485,rs11726949,rs12512308,rs7438961,rs998538)和四个CD46 SNP(rs12138764,rs2466571,rs2796278,rs7545126)进行基因分型。使用χ2检验比较患者和对照组之间的等位基因和基因型频率。分析按性别,人类白细胞抗原(HLA)-B27和强直性脊柱炎状态进行分层。结果:发现CFI基因中的Rs7356506对AAU具有保护作用。 A等位基因(p = 0.003,pc = 0.03,OR = 0.684,CI 0.534至0.876)和AA纯合子(p = 0.004,pc = 0.04,OR = 0.624,CI 0.452至0.862)的频率显着增加与对照组相比)。根据AAU的性别和HLA-B27状况进行的分层分析也揭示了与CFI-rs7356506的关联。 CD46的所有测试SNP均与AAU无关。结论:这项研究揭示了AAU和CFI-rs7356506之间的显着关联,表明CFI参与了AAU的发病机理,并且其对AAU的影响可能取决于性别和HLA-B27状态。

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