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类风湿关节炎(RA)的病因、临床和药物经济学评估。

Pathogenetic, clinical and pharmaco-economic assessment in rheumatoid arthritis (RA).

机构信息

Division of Rheumatology, Institute of Rheumatology, School of Medicine, Catholic University of the Sacred Heart-CIC, Via Moscati 31, Rome, Italy.

出版信息

Intern Emerg Med. 2011 Oct;6 Suppl 1:11-5. doi: 10.1007/s11739-011-0668-6.

DOI:10.1007/s11739-011-0668-6
PMID:22009608
Abstract

Rheumatoid arthritis (RA) has become one of the most studied autoimmune chronic inflammatory diseases (ACIDs), either from the pathogenetic or from the therapeutic point of view. It is recognized that synovial fibroblasts, TH1 and TH17 cells likely play along with the B cells the most relevant role. The disease has a polygenic background that characterizes the seropositive and the seronegative subsets. Over the years, we realized that no more than 15-20% of long-standing RA (LSRA) treated with conventional drugs can reach full remission, whereas the most recent data in early RA (ERA) have demonstrated that 40-60% can be put into clinical and biological remission. This of course is of crucial importance to avoid any progression of the structural damage that leads to functional disability. If we consider that a disability index score (Health Assessment Questionnaire 0-3) of a severe arthritis can cost up to 21,000 EUs, while a mild disease will cost not more than 5,500 EUs per year, it appears very clear that a low disease activity (LDA) or a remission state (Rem) should be the aim in each single patient, in order to keep the workability and maintain the productivity. This is and should be the major aim in each RA patient.

摘要

类风湿关节炎 (RA) 已成为研究最多的自身免疫性慢性炎症性疾病 (ACIDs) 之一,无论是从发病机制还是治疗角度来看。人们认识到,滑膜成纤维细胞、TH1 和 TH17 细胞可能与 B 细胞一起发挥最相关的作用。该疾病具有多基因背景,可将血清阳性和血清阴性亚组区分开来。多年来,我们意识到,在接受常规药物治疗的长期 RA (LSRA) 中,只有不超过 15-20%的患者能够达到完全缓解,而在早期 RA (ERA) 的最新数据中表明,40-60%的患者可以达到临床和生物学缓解。这对于避免导致功能障碍的结构损伤进展当然至关重要。如果我们考虑到严重关节炎的残疾指数评分(健康评估问卷 0-3)可能高达 21,000 欧元,而轻度疾病每年的费用不超过 5,500 欧元,那么很明显,低疾病活动度 (LDA) 或缓解状态 (Rem) 应该成为每个患者的目标,以保持工作能力并维持生产力。这是并且应该是每个 RA 患者的主要目标。

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本文引用的文献

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Arch Oral Biol. 2011 Nov;56(11):1412-8. doi: 10.1016/j.archoralbio.2011.05.005. Epub 2011 Jun 16.
2
Implementation of a treat-to-target strategy in very early rheumatoid arthritis: results of the Dutch Rheumatoid Arthritis Monitoring remission induction cohort study.在极早期类风湿关节炎中实施达标治疗策略:荷兰类风湿关节炎监测缓解诱导队列研究结果
Arthritis Rheum. 2011 Oct;63(10):2865-72. doi: 10.1002/art.30494.
3
The potential role of Th17 in mediating the transition from acute to chronic autoimmune inflammation: rheumatoid arthritis as a model.
早期类风湿关节炎作为缓解的预测指标:一项多中心真实前瞻性研究。
Ann Rheum Dis. 2013 Jun;72(6):858-62. doi: 10.1136/annrheumdis-2012-201456. Epub 2012 Jul 13.
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Discov Med. 2011 May;11(60):413-24.
4
B-cell subsets in the joint compartments of seropositive and seronegative rheumatoid arthritis (RA) and No-RA arthritides express memory markers and ZAP70 and characterize the aggregate pattern irrespectively of the autoantibody status.在血清阳性和血清阴性类风湿关节炎(RA)和非 RA 关节炎的关节隔室中,B 细胞亚群表达记忆标记物和 ZAP70,并且无论自身抗体状态如何,都具有聚集模式的特征。
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