首页> 外文OA文献 >Poremećaji genskoga izražaja u bolesnika s juvenilnim seronegativnim spondiloartropatijama Distinctive gene expression in patients with juvenile seronegative spondyloarthtopathy
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Poremećaji genskoga izražaja u bolesnika s juvenilnim seronegativnim spondiloartropatijama Distinctive gene expression in patients with juvenile seronegative spondyloarthtopathy

机译:青少年血清阴性脊柱关节病患者基因表达障碍青少年血清阴性脊柱关节病患者的特异性基因表达

摘要

Introduction: Juvenile spondyloarthritis (jSpA) refers to spectrum of unpredictableudinflammatory diseases with overlapping features in children younger than 16 years. There is audstrong association of jSpA with HLA-B27 genotype, but many studies shows that otherudgenetic factors, of which we have little or no knowledge, plays a role in the development ofudjSpA. ----- Patients and methods: In this study participated 45 children with obtained HLA genotypeudand diagnosis of jSpA according to ILAR criteria, as well as 11 children with other forms ofudJIA and 12 children without diagnosis of inflammatory disease. DNA microarray geneudexpression was preformed in 11 patients with jSpA and in 4 participants without diagnosis ofudinflammatory disease, along with bioinformatic analysis of retrieved data. Carefully selecteduddifferentially expressed genes where analyzed by qRT-PCR in all participants. ----- Results: Microarray results and bioinformatic analysis revealed 745 differentially expressedudgenes involved in various inflammatory processes in jSpA patients, while qRT-PCR analysisudconfirmed data universality and specificity. ----- Conclusion: Our findings showed that jSpA is polygenic disease with malfunction in antigenudrecognition and activation of immunological response, in migration of inflammatory cells andudin regulation of the immune system. Results of our study can be used for further investigationudof disease patophisiology and new treatment options.
机译:简介:少年性脊柱关节炎(jSpA)是指16岁以下儿童中具有重叠特征的不可预测的发炎性疾病。 jSpA与HLA-B27基因型之间有很强的联系,但是许多研究表明,我们所知甚少或根本不了解的其他预算因素在 udjSpA的发生中发挥了作用。 -----患者和方法:本研究纳入了45名根据ILAR标准获得HLA基因型 jSpA诊断的儿童,以及11名其他形式 udJIA的儿童和12名未诊断出炎性疾病的儿童。在11名jSpA患者和4名未诊断出 uditis疾病的参与者中进行了DNA芯片基因表达减退,同时对检索到的数据进行了生物信息学分析。仔细选择差异表达的基因,通过qRT-PCR分析所有参与者。 -----结果:芯片结果和生物信息学分析显示jSpA患者中有745种差异表达参与多种炎症过程的肿瘤,而qRT-PCR分析则证实了数据的普遍性和特异性。 -----结论:我们的研究结果表明jSpA是一种多基因疾病,在抗原未识别和免疫应答激活,炎性细胞迁移和 udin免疫系统调节方面均存在功能障碍。我们的研究结果可用于进一步研究疾病的病因学和新的治疗选择。

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    Lamot Lovro;

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  • 年度 2014
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