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血清自身抗体在系统性硬化症患者中的临床情况

Clinical setting of patients with systemic sclerosis by serum autoantibodies.

作者信息

Picillo U, Migliaresi S, Marcialis M R, Ferruzzi A M, Tirri G

机构信息

Institute of Clinical Medicine, Rheumatology Unit, Faculty of Medicine 2nd University of Naples, Italy.

出版信息

Clin Rheumatol. 1997 Jun;16(4):378-83. doi: 10.1007/BF02242455.

DOI:10.1007/BF02242455
PMID:9259252
Abstract

Associations of antinuclear (ANA) and anticardiolipin (aCL) antibodies with clinical manifestations were analyzed in patients with systemic sclerosis (SSc). We studied 105 SSc patients: 28 had limited cutaneous SSc (lcSSc) involving fingers; 36 had intermediate cutaneous SSc involving limbs and face; 33 had diffuse cutaneous SSc (dcSSc) involving the trunk; 8 had a sclerosis sine scleroderma. Clinical manifestations and instrumental and laboratory findings were considered to calculate a disease score. Serum anticentromere (ACA), anti-topoisomerase I (anti-topo I) antibodies, and aCL (of IgG/IgA/IgM classes) were investigated by conventional methods. ACA positive patients (n=18), compared to ACA negative, showed higher prevalence of IcSSc (p < 0.001), lower prevalence of restrictive ventilatory defect (p=0.006), and lower disease score (p=0.008). Anti-topo I positive patients (n= 70) showed lower prevalence of lcSSc (p =0.001) compared to anti-topo I negative. In aCL positive patients (n=27) widespread skin and visceral involvement occurred more frequently than in aCL negative. The association with myocardial ischemia or necrosis (p=0.010) was significant. Occurrence of ACA excluded the coexistence of anti-topo I (p < 0.001), and aCL (p=0.037). aCL positive patients showed higher disease score in comparison with ACA positive patients (p=0.003). In conclusion ACA recognize patients with a mild disease. aCL in contrast to ACA are better than anti-topo I in recognizing the most severe pictures of SSc.

摘要

分析了抗核(ANA)和抗心磷脂(aCL)抗体与系统性硬化症(SSc)患者临床表现之间的关联。我们研究了105例SSc患者:28例为局限型皮肤SSc(lcSSc),累及手指;36例为中间型皮肤SSc,累及四肢和面部;33例为弥漫型皮肤SSc(dcSSc),累及躯干;8例为无硬皮病的硬化症。考虑临床表现、仪器检查和实验室检查结果来计算疾病评分。采用传统方法检测血清抗着丝点(ACA)、抗拓扑异构酶I(抗topo I)抗体以及IgG/IgA/IgM类别的aCL。与ACA阴性患者相比,ACA阳性患者(n = 18)中lcSSc的患病率更高(p < 0.001),限制性通气功能障碍的患病率更低(p = 0.006),疾病评分更低(p = 0.008)。与抗topo I阴性患者相比,抗topo I阳性患者(n = 70)中lcSSc的患病率更低(p = 0.001)。在aCL阳性患者(n = 27)中,皮肤和内脏广泛受累的情况比aCL阴性患者更常见。与心肌缺血或坏死的关联具有显著性(p = 0.010)。ACA阳性排除了抗topo I(p < 0.001)和aCL(p = 0.037)同时存在的情况。与ACA阳性患者相比,aCL阳性患者的疾病评分更高(p = 0.003)。总之,ACA可识别病情较轻的患者。与ACA相比,aCL在识别最严重的SSc病例方面优于抗topo I。

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本文引用的文献

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Patients with anticentromere antibodies, clinical features, diagnoses and evolution.患有抗着丝点抗体的患者、临床特征、诊断及病情演变。
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Anticardiolipin, anticentromere and anti-Scl-70 antibodies in patients with systemic sclerosis and severe digital ischaemia.系统性硬化症合并严重指端缺血患者的抗心磷脂抗体、抗着丝点抗体和抗Scl-70抗体
Ann Rheum Dis. 1994 Aug;53(8):540-2. doi: 10.1136/ard.53.8.540.
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