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本文引用的文献

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A prospective approach to investigating the natural history of preclinical rheumatoid arthritis (RA) using first-degree relatives of probands with RA.一种利用类风湿关节炎(RA)先证者的一级亲属来研究临床前期类风湿关节炎自然史的前瞻性方法。
Arthritis Rheum. 2009 Dec 15;61(12):1735-42. doi: 10.1002/art.24833.
2
An eight-gene blood expression profile predicts the response to infliximab in rheumatoid arthritis.一种八基因血液表达谱可预测类风湿关节炎对英夫利昔单抗的应答。
PLoS One. 2009 Oct 22;4(10):e7556. doi: 10.1371/journal.pone.0007556.
3
Clinical approaches to early inflammatory arthritis.早期炎症性关节炎的临床处理方法。
Nat Rev Rheumatol. 2009 Nov;5(11):627-33. doi: 10.1038/nrrheum.2009.203. Epub 2009 Sep 29.
4
Blood autoantibody and cytokine profiles predict response to anti-tumor necrosis factor therapy in rheumatoid arthritis.血液自身抗体和细胞因子谱可预测类风湿关节炎对抗肿瘤坏死因子治疗的反应。
Arthritis Res Ther. 2009;11(3):R76. doi: 10.1186/ar2706. Epub 2009 May 21.
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Recent progress in rheumatoid arthritis genetics: one step towards improved patient care.类风湿关节炎遗传学的最新进展:向改善患者护理迈进的一步。
Curr Opin Rheumatol. 2009 May;21(3):262-71. doi: 10.1097/BOR.0b013e32832a2e2d.
6
Evidence that cytokines play a role in rheumatoid arthritis.细胞因子在类风湿性关节炎中起作用的证据。
J Clin Invest. 2008 Nov;118(11):3537-45. doi: 10.1172/JCI36389.
7
Protein biochip array technology for cytokine profiling predicts etanercept responsiveness in rheumatoid arthritis.用于细胞因子谱分析的蛋白质生物芯片阵列技术可预测类风湿关节炎患者对依那西普的反应性。
Clin Exp Immunol. 2008 Aug;153(2):188-95. doi: 10.1111/j.1365-2249.2008.03691.x. Epub 2008 Jun 18.
8
Use of multiple biomarkers to improve the prediction of death from cardiovascular causes.使用多种生物标志物改善心血管病因死亡的预测。
N Engl J Med. 2008 May 15;358(20):2107-16. doi: 10.1056/NEJMoa0707064.
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Antibodies to citrullinated proteins in arthritis: pathology and promise.关节炎中瓜氨酸化蛋白抗体:病理学与前景
Curr Opin Rheumatol. 2008 May;20(3):300-5. doi: 10.1097/BOR.0b013e3282fbd22a.
10
Association of rheumatoid factor and anti-cyclic citrullinated peptide positivity, but not carriage of shared epitope or PTPN22 susceptibility variants, with anti-tumour necrosis factor response in rheumatoid arthritis.类风湿关节炎中类风湿因子和抗环瓜氨酸肽阳性与抗肿瘤坏死因子反应相关,但共同表位或PTPN22易感变异的携带情况与之无关。
Ann Rheum Dis. 2009 Jan;68(1):69-74. doi: 10.1136/ard.2007.084715. Epub 2008 Mar 28.

类风湿关节炎的生物标志物:实现个体化诊疗

Biomarkers for rheumatoid arthritis: making it personal.

作者信息

Lindstrom Tamsin M, Robinson William H

机构信息

Geriatric Research Education and Clinical Center (GRECC), VA Palo Alto Health Care System, Palo Alto, CA, USA.

出版信息

Scand J Clin Lab Invest Suppl. 2010;242:79-84. doi: 10.3109/00365513.2010.493406.

DOI:10.3109/00365513.2010.493406
PMID:20515283
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3417774/
Abstract

Effective treatment of rheumatoid arthritis (RA) has been hampered by the heterogeneity of the disease. Although early intervention can result in disease remission, it requires early diagnosis - and current diagnostic tests are not sufficiently accurate or sensitive in the early stages of RA. As a result, RA is typically diagnosed only once damage to the joints has already begun, a time at which the window for optimal treatment may have been missed. Furthermore, a significant proportion of RA patients do not respond to any given therapeutic. Research efforts are increasingly focused on discovery of biomarkers that enable early diagnosis and stratification of RA, and thus the implementation of timely, targeted therapy. Biomarkers have the potential to transform the management of RA by enabling not only early diagnosis, but also assessment and prediction of disease severity, selection of therapy, and monitoring of response to therapy. In this mini review, we discuss the development of molecular biomarkers for RA.

摘要

类风湿关节炎(RA)的异质性阻碍了其有效治疗。尽管早期干预可使疾病缓解,但这需要早期诊断——而目前的诊断测试在RA早期阶段的准确性和敏感性不足。因此,RA通常在关节损伤已经开始时才被诊断出来,此时可能已经错过了最佳治疗时机。此外,相当一部分RA患者对任何给定的治疗方法都没有反应。研究工作越来越集中在发现能够实现RA早期诊断和分层的生物标志物,从而实施及时、有针对性的治疗。生物标志物不仅有可能通过实现早期诊断来改变RA的管理,还能对疾病严重程度进行评估和预测、选择治疗方法以及监测治疗反应。在本综述中,我们讨论了RA分子生物标志物的发展。