Antineutrophil cytoplasmic antibodies in primary Sjögren's syndrome: prevalence and clinical significance.

J Font, M Ramos-Casals, R Cervera, X Bosch, E Mirapeix, M García-Carrasco, R M Morlà, M Ingelmo
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引用次数: 66

Abstract

Objective: To evaluate the prevalence of cytoplasmic (c) and perinuclear (p) antineutrophil cytoplasmic antibodies (ANCA) in patients with primary Sjogren's syndrome (SS), and to correlate the presence of ANCA with extraglandular and immunological manifestations related to SS.

Methods: In a cross-sectional study, we included 82 consecutive patients (75 female and seven male; mean age 61 yr; range 33-87 yr) attending our unit. All patients fulfilled four or more of the diagnostic criteria for SS proposed by the European Community Study Group in 1993. Extraglandular manifestations such as arthralgia and/or arthritis, Raynaud's phenomenon, autoimmune thyroiditis, peripheral neuropathy, renal involvement and cutaneous vasculitis were also recorded. Serum samples were examined by indirect immunofluorescence (IIF) and by ELISA using as substrates myeloperoxidase (MPO) and proteinase 3 (PR3).

Results: ANCA were detected in nine (11%) patients: seven had pANCA and two an atypical pattern. These two atypical ANCA became cANCA when paraformaldehyde fixation was applied. ELISA findings showed that two patients had antibodies against MPO, and no patient had antibodies to PR3. The most common extraglandular manifestations in the ANCA-positive patients were articular involvement in six (66%) patients, peripheral neuropathy in five (55%), Raynaud's phenomenon in four (44%) and cutaneous vasculitis in four (44%). Of the four patients with cutaneous vasculitis and ANCA, two had a mononuclear inflammatory vascular disease (MIVD) in the biopsy specimen. When compared with patients without ANCA, those with these antibodies had a higher prevalence of cutaneous vasculitis (44% vs 8%, P = 0.01), Raynaud's phenomenon (44% vs 8%, P = 0.01) and peripheral neuropathy (55% vs 7%, P < 0.001).

Conclusion: ANCA positivity can be found in patients with primary SS and its detection is associated with the presence of clinical manifestations attributable to vascular involvement (cutaneous vasculitis, peripheral neuropathy and Raynaud's phenomenon).

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抗中性粒细胞胞浆抗体在原发性Sjögren综合征中的患病率及临床意义。
目的:评估原发性干燥综合征(SS)患者胞浆(c)和核周(p)抗中性粒细胞胞浆抗体(ANCA)的患病率,并探讨ANCA的存在与SS相关的腺外和免疫表现之间的关系。方法:在一项横切面研究中,我们纳入了82例连续患者(75名女性和7名男性;平均年龄61岁;33-87岁,在我们部队服役。所有患者均符合1993年欧洲共同体研究小组提出的四项或以上的SS诊断标准。腺外表现如关节痛和/或关节炎、雷诺现象、自身免疫性甲状腺炎、周围神经病变、肾脏受累和皮肤血管炎也被记录。以骨髓过氧化物酶(MPO)和蛋白酶3 (PR3)为底物,采用间接免疫荧光(IIF)和酶联免疫吸附试验(ELISA)检测血清样品。结果:9例(11%)患者检测到ANCA,其中7例为pANCA, 2例为非典型。应用多聚甲醛固定后,这两种非典型ANCA变为cANCA。ELISA结果显示2例患者有MPO抗体,无PR3抗体。anca阳性患者最常见的腺外表现为6例(66%)的关节受累,5例(55%)的周围神经病变,4例(44%)的雷诺现象和4例(44%)的皮肤血管炎。在4例皮肤血管炎和ANCA患者中,2例活检标本显示单核炎症性血管疾病(MIVD)。与无ANCA的患者相比,有这些抗体的患者有更高的皮肤血管炎(44%比8%,P = 0.01)、雷诺现象(44%比8%,P = 0.01)和周围神经病变(55%比7%,P < 0.001)的患病率。结论:原发性SS患者可发现ANCA阳性,其检测与血管受累的临床表现(皮肤血管炎、周围神经病变、雷诺现象)有关。
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