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Investigation of rheumatoid arthritis genetic susceptibility markers in the early rheumatoid arthritis study further replicates the TRAF1 association with radiological damage

机译:类风湿性关节炎的调查早期类风湿性关节炎研究中的遗传易感性标志物进一步复制了TRaF1与放射性损伤的关联

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摘要

Objective. The TRAF1 genetic region conferring susceptibility to rheumatoid arthritis (RA) has been reported to associate with radiological damage. We aimed to test RA genetic susceptibility markers for association with a continuous measure of radiological damage over time using longitudinal modeling techniques. Methods. Sixty-seven RA susceptibility variants were genotyped in 474 patients in the Early Rheumatoid Arthritis Study (ERAS) using Sequenom MassArray technology. Correlation between genetic markers and Larsen score was assessed longitudinally using zero-inflated negative binomial regression to include repeat measurements in the same individual at different timepoints. Genetic markers associated with radiological damage in ERAS were tested using the same modeling techniques on previously published data from the Norfolk Arthritis Register (NOAR). Results. The single marker associated longitudinally with Larsen score in ERAS (p = 0.02) and in NOAR (p = 0.04) was rs2900180 at the TRAF1 locus. Analysis of individual timepoints in ERAS showed that rs2900180 displays its effect primarily on the extent of Larsen score early in the disease course. Combined longitudinal analysis of the 2 cohorts suggests further association of several loci with Larsen score (KIF5A, PTPN22, AFF3, TAGAP) and therefore a significant accumulation of RA severity markers among RA susceptibility markers (p = 0.016). Conclusion. The marker rs2900180 is associated with the extent of radiological damage in the ERAS cohort. This represents the second independent study correlating rs2900180 at the TRAF1 locus with radiological severity in RA. Replication in a large dataset is required to establish the role of other RA susceptibility loci in disease severity. Copyright © 2013 The Journal of Rheumatology.
机译:目的。据报道,TRAF1遗传区赋予类风湿性关节炎(RA)的易感性与放射损伤有关。我们的目标是使用纵向建模技术测试RA遗传易感性标志物,以随着时间的推移连续评估放射损伤。方法。使用Sequenom MassArray技术在早期类风湿性关节炎研究(ERAS)中对474名患者的67种RA敏感性变异进行了基因分型。使用零膨胀负二项式回归来纵向评估遗传标记与Larsen评分之间的相关性,以包括同一个人在不同时间点的重复测量。使用相同的建模技术,根据诺福克关节炎登记处(NOAR)先前发布的数据,对与ERAS中的放射损伤相关的遗传标记进行了测试。结果。在TRAF1位点,与ERAS(p = 0.02)和NOAR(p = 0.04)的Larsen评分纵向相关的单个标记是rs2900180。对ERAS中各个时间点的分析表明,rs2900180主要在疾病过程的早期对Larsen评分的程度发挥作用。对这两个队列的纵向综合分析表明,多个基因座与Larsen评分(KIF5A,PTPN22,AFF3,TAGAP)进一步相关,因此在RA易感性标记之间存在大量RA严重性标记(p = 0.016)。结论。标记rs2900180与ERAS队列中的放射损伤程度有关。这代表了第二项独立研究,将TRAF1基因座处的rs2900180与RA的放射学严重程度相关联。需要在大型数据集中复制才能确定其他RA易感基因座在疾病严重程度中的作用。版权所有©2013风湿病杂志。

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