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日本系统性硬化症患者血清抗核抗体的临床及预后关联

Clinical and prognostic associations based on serum antinuclear antibodies in Japanese patients with systemic sclerosis.

作者信息

Kuwana M, Kaburaki J, Okano Y, Tojo T, Homma M

机构信息

Department of Medicine, Keio University School of Medicine, Tokyo, Japan.

出版信息

Arthritis Rheum. 1994 Jan;37(1):75-83. doi: 10.1002/art.1780370111.

Abstract

OBJECTIVE

To clarify the clinical features and prognosis of systemic sclerosis (SSc) based on serum antinuclear antibodies (ANA).

METHODS

We studied 275 consecutive Japanese patients newly diagnosed as having SSc, who were first evaluated during the period 1971-1990. Eight SSc-related ANA were identified using indirect immunofluorescence, double immunodiffusion, or immunoprecipitation assays. Clinical and prognostic features were retrospectively analyzed in patient groups, categorized by their serum ANA.

RESULTS

Cumulative survival rates at 10 years after diagnosis of SSc were 93% in patients with anticentromere antibodies (ACA), 72% in those with anti-U1 RNP, 66% in those with anti-DNA topoisomerase I (anti-topo I), and 30% in those with anti-RNA polymerases I, II, and III (anti-RNAP). Major organ involvement linked to cause of death included biliary cirrhosis in patients with ACA, isolated pulmonary arterial hypertension and cerebral hemorrhage in those with anti-U1 RNP, pulmonary interstitial fibrosis in those with anti-topo I, and cardiac and renal involvement in those with anti-RNAP.

CONCLUSION

Determinations of serum ANA in SSc patients are useful in predicting organ involvement and long-term outcome.

摘要

目的

基于血清抗核抗体(ANA)阐明系统性硬化症(SSc)的临床特征及预后。

方法

我们研究了1971年至1990年期间首次接受评估的275例新诊断为SSc的连续日本患者。使用间接免疫荧光、双向免疫扩散或免疫沉淀试验鉴定了8种与SSc相关的ANA。对按血清ANA分类的患者组的临床和预后特征进行回顾性分析。

结果

SSc诊断后10年的累积生存率,抗着丝点抗体(ACA)患者为93%,抗U1核糖核蛋白(RNP)患者为72%,抗DNA拓扑异构酶I(抗拓扑异构酶I)患者为66%,抗RNA聚合酶I、II和III(抗RNAP)患者为30%。与死亡原因相关的主要器官受累包括ACA患者的胆汁性肝硬化、抗U1 RNP患者的孤立性肺动脉高压和脑出血、抗拓扑异构酶I患者的肺间质纤维化,以及抗RNAP患者的心脏和肾脏受累。

结论

测定SSc患者的血清ANA有助于预测器官受累情况和长期预后。

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