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Antiphospholipid antibodies in primary Sjogren's syndrome: prevalence and clinical significance in a series of 74 patients.

机译:原发性干燥综合征中的抗磷脂抗体:74例患者的患病率和临床意义。

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摘要

The aim of this study is to determine prevalence, clinical significance of antiphospholipid antibodies (aPL) including anticardiolipin antibodies (aCL), anti-beta2GP1 and lupus anticoagulant (LA) in a cohort of 74 patients with primary Sjogren's syndrome (pSS) according to revised European criteria. aPL were found in 25 (34%) patients; IgG in 23 (12 had low titres, six moderate titres and five high titres) and IgM in five (three and two had respectively moderate and high titres). Eight (11%) patients were found to have LA; anti-beta2GP1 antibodies were detected only in three (4%) patients. Only two patients with LA, aPL and beta2GP1 had recurrent venous thrombosis. One patient with moderate titres of aPL exhibited recurrent spontaneous foetal losses. Peripheral neuropathies without cryoglobulinemia were more frequent in the aPL group. Other systemic involvements of pSS were the same in both groups with or without aPL. Patients with aPL have more concurrent immunological diseases such as thyroiditis andprimary biliary cirrhosis and a higher prevalence of hypergammaglobulinemia (P < 0.05). Even if aPL prevalence reached 30% in pSS, titres were usually low, with a close correlation with hypergammaglobulinemia but not with antiphospholipid syndrome, which is related to positivity of both LA and aPL.
机译:这项研究的目的是根据修订版确定74例原发性干燥综合征(pSS)患者的抗磷脂抗体(aPL)(包括抗心磷脂抗体(aCL),抗β2GP1和狼疮抗凝剂(LA))的患病率,临床意义欧洲标准。在25(34%)位患者中发现了aPL; IgG中的23种抗体(12滴度低,6种中等滴度和5种高滴度)和IgM的5种抗体(3种和2种滴度分别为中等和高滴度)。发现八名(11%)患者患有洛杉矶;仅在三名(4%)患者中检测到了抗beta2GP1抗体。仅两名LA,aPL和beta2GP1的LA患者复发静脉血栓形成。一名具有中等滴度aPL的患者表现出反复自然流产。在aPL组中,无冷球蛋白血症的周围神经病变更为常见。在有或没有aPL的两组中,pSS的其他全身性参与都是相同的。患有aPL的患者有更多的并发免疫疾病,例如甲状腺炎和原发性胆汁性肝硬化,以及高球蛋白球蛋白血症的患病率更高(P <0.05)。即使在pSS中aPL的患病率达到30%,滴度通常也很低,与高球蛋白血症相关,而与抗磷脂综合征无关,这与LA和aPL的阳性有关。

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