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在早期类风湿关节炎研究中对类风湿关节炎遗传易感性标记物的研究进一步复制了 TRAF1 与放射学损伤的关联。

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

机构信息

Arthritis Research UK Epidemiology Unit, Manchester Academic Health Science Centre, The University of Manchester, Manchester, UK.

出版信息

J Rheumatol. 2013 Feb;40(2):144-56. doi: 10.3899/jrheum.121034. Epub 2012 Dec 15.

Abstract

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.

摘要

目的

已报道 TRAF1 基因区域与类风湿关节炎(RA)的放射学损伤相关。我们旨在使用纵向建模技术,测试 RA 遗传易感性标记物与随时间推移的放射学损伤的连续测量值之间的关联。

方法

使用 Sequenom MassArray 技术,对早期类风湿关节炎研究(ERAS)中的 474 名患者进行 67 个 RA 易感性变体的基因分型。使用零膨胀负二项式回归评估遗传标记物与 Larsen 评分之间的相关性,该方法包括在不同时间点对同一个体进行重复测量。使用相同的建模技术,对先前发表的诺福克关节炎登记处(NOAR)的数据进行测试,以确定与放射学损伤相关的遗传标记物。

结果

在 ERAS 中,与 Larsen 评分呈纵向相关(p = 0.02)且与 NOAR 相关(p = 0.04)的唯一标记物是 TRAF1 基因座上的 rs2900180。ERAS 中个体时间点的分析表明,rs2900180 主要在疾病早期对 Larsen 评分的程度产生影响。对这两个队列的综合纵向分析表明,几个基因座与 Larsen 评分进一步相关(KIF5A、PTPN22、AFF3、TAGAP),因此,RA 易感性标记物中 RA 严重程度标记物的显著积累(p = 0.016)。

结论

rs2900180 标记物与 ERAS 队列的放射学损伤程度相关。这是第二个独立研究,将 TRAF1 基因座上的 rs2900180 与 RA 放射学严重程度相关联。需要在大型数据集上进行复制,以确定其他 RA 易感性基因座在疾病严重程度中的作用。

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