Advances in the genetics of rheumatoid arthritis point to subclassification into distinct disease subsets.

Advances in the genetics of rheumatoid arthritis point to subclassification into distinct disease subsets.
复制标题

类风湿关节炎的遗传学进展将亚分类分为不同的疾病子集。

DOI:
10.1186/ar2384
复制
发表时间:
2008
影响因子:
4.9
通讯作者:
Huizinga TW
Huizinga TW
中科院分区:
医学2区
文献类型:
--
作者:
van der Helm-van Mil AH;Huizinga TW

文献摘要

参考文献

被引文献

相似文献

在过去的几年中,类风湿性关节炎(RA)易感性的遗传学研究取得了相当大的进展。几十年来,HLA-DRB1 等位基因是唯一广泛复制的遗传因素,但现在已发现更多易患 RA 的遗传风险因素。有趣的是,观察到的几个遗传变异赋予抗瓜氨酸肽抗体(ACPA)阳性 RA 的风险,并且两个变异可能仅限于 ACPA 阴性 RA,这表明需要对 RA 进行亚分类。当前的手稿评论最近发现了易患 ACPA 阳性 RA 和 ACPA 阴性 RA 的遗传因素。此外,尽管很少进行探索,但影响病程严重程度的遗传变异也得到了讨论。
In the past few years considerable advances have been made in the genetics of susceptibility to rheumatoid arthritis (RA). For decades the HLA-DRB1 alleles were the only extensively replicated genetic factor, but more genetic risk factors have now been identified that predispose to RA. Interestingly, several of the observed genetic variants conferred risk to anticitrulline-peptide antibody (ACPA)-positive RA and two variants may be restricted to ACPA-negative RA, pointing to the need for subclassification of RA. The current manuscript reviews recently identified genetic factors predisposing to ACPA-positive RA and ACPA-negative RA. Additionally, although being scarcely explored, genetic variants affecting the severity of disease course are discussed.
DOI: 10.1086/516736
发表时间: 2007-05-01
影响因子: 9.8
作者:
Kallberg, Henrik;Padyukov, Leonid;Alfredsson, Lars
通讯作者: Alfredsson, Lars
DOI: 10.1186/ar1889
发表时间: 2006
影响因子: 4.9
作者:
Hoppe B;Häupl T;Gruber R;Kiesewetter H;Burmester GR;Salama A;Dörner T
通讯作者: Dörner T
DOI: 10.1186/ar1164
发表时间: 2004
影响因子: 4.9
作者:
Dörr S;Lechtenböhmer N;Rau R;Herborn G;Wagner U;Müller-Myhsok B;Hansmann I;Keyszer G
通讯作者: Keyszer G
DOI: 10.1136/ard.2006.061390
发表时间: 2007-06-01
影响因子: 27.4
作者:
Garnier, Sophie;Dieude, Philippe;Cornelis, Francois
通讯作者: Cornelis, Francois
DOI: 10.1002/art.22814
发表时间: 2007-08-01
影响因子: --
作者:
Marinou, I.;Healy, J.;Wilson, A. G.
通讯作者: Wilson, A. G.