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日本的银屑病关节炎:临床特征差异与精准医学方法

Psoriatic arthritis in Japan: difference in clinical features and approach to precision medicine.

作者信息

Tanaka Yoshiya

机构信息

The First Department of Internal Medicine, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan.

出版信息

Clin Exp Rheumatol. 2016 Jul-Aug;34(4 Suppl 98):49-52. Epub 2016 Jul 20.

PMID:27586804
Abstract

Psoriatic arthritis (PsA) is a chronic and progressive inflammatory arthritis that is common among patients with psoriasis, often resulting in permanent damage of joints and spines. Recent report indicates that the prevalence of PsA among Japanese patients with psoriasis is 14.3%, which is similar or slightly less than that of PsA in Caucasian, 6-42%. Skin disorders precede arthritis in 60-80% of Japanese patients with PsA and oligoarthritis or polyarthritis is the dominant pattern of them. The genotypic backgrounds appear different among Japanese and Caucasians. Biological DMARDs (bDMARDs) targeting cytokines IL-12/IL-23, TNF and IL-17 involved in the pathogenesis of PsA, have been emerging for the treatment. Although background characteristics are various among studies, anti-IL-17 seemed to be slightly better in Japanese than in global, whereas anti-IL-12/23 and anti-TNF tended to be better in global than in Japanese. Because PsA is a clinically heterogeneous disorder, we have tried to classify PsA by phenotypic differences of peripheral lymphocyte using 8-color flow cytometry and found that PsA can be divided to four types, activated Th17-dominant, Th1-dominant, both of them and neither of them. We currently try to treat patients with different bDMARDs based on the difference of lymphocyte phenotype, which may lead to precision medicine of PsA.

摘要

银屑病关节炎(PsA)是一种慢性进行性炎症性关节炎,在银屑病患者中很常见,常导致关节和脊柱的永久性损伤。最近的报告表明,日本银屑病患者中PsA的患病率为14.3%,与白种人中PsA的患病率相似或略低,白种人中PsA的患病率为6%-42%。在60%-80%的日本PsA患者中,皮肤疾病先于关节炎出现,其中少关节炎或多关节炎是主要类型。日本人和白种人的基因背景似乎有所不同。针对参与PsA发病机制的细胞因子IL-12/IL-23、TNF和IL-17的生物性疾病修饰抗风湿药物(bDMARDs)已逐渐用于治疗。尽管各研究中的背景特征各不相同,但抗IL-17药物在日本患者中的疗效似乎略优于全球水平,而抗IL-12/23和抗TNF药物在全球的疗效往往优于日本。由于PsA是一种临床异质性疾病,我们尝试使用8色流式细胞术根据外周淋巴细胞的表型差异对PsA进行分类,发现PsA可分为四种类型:活化的Th17主导型、Th1主导型、两者皆有以及两者皆无。我们目前正尝试根据淋巴细胞表型的差异,使用不同的bDMARDs治疗患者,这可能会带来PsA的精准医学。

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