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Value of IgA anticardiolipin and anti-beta(2)-glycoprotein I antibody testing in patients with pregnancy morbidity

机译:IgA抗心磷脂和抗β(2)-糖蛋白I抗体检测在妊娠合并症患者中的价值

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摘要

Objective: To study the prevalence of IgA antiphospholipid antibodies, particularly anticardiolipin antibodies (aCL) and anti-β2-glycoprotein I (aβ2GPI), in a cohort of patients with pregnancy morbidity.Patients and methods: Serum samples from four groups of patients were studied by an in house enzyme linked immunosorbent assay (ELISA). Group I: 28 patients with primary antiphospholipid syndrome (PAPS) (median age 32.5 years, range 25–34). Twelve patients had a history of thrombosis. All were positive for IgG/M aCL or lupus anticoagulant (LA), or both. Group II: 28 patients with unexplained pregnancy morbidity (median age 35 years, range 23–48). Seven had history of thrombosis. Nine patients were positive for IgG/M aCL. None from this group fulfilled Sapporo criteria for APS. Group III: 28 patients with systemic lupus erythematosus (SLE) (median age 34 years, range 25–52). Eleven had a history of thrombosis. Twenty one patients had IgG/M aCL and/or LA, but only 19 fulfilled Sapporo criteria for APS.Results: IgA aCL were found in 12, 6, and 14 patients from the groups with PAPS, unexplained pregnancy morbidity, and SLE, respectively. Most patients had these antibodies together with IgG/IgM aCL. Three patients from the group with unexplained pregnancy morbidity and two with SLE had IgA aCL alone. IgA aβ2GPI was present in one patient from each group. All IgA aβ2GPI were present together with IgG and/or IgM aβ2GPI.Conclusions: The prevalence of IgA aCL is high in patients with pregnancy morbidity, although IgA aCL are usually present together with IgG and/or IgM aCL. IgA aβ2GPI are not useful in identifying additional women with APS and pregnancy morbidity.
机译:目的:研究一组IgA抗磷脂抗体,尤其是抗心磷脂抗体(aCL)和抗β2-糖蛋白I(aβ2GPI)在妊娠合并症患者中的患病率和方法:研究了四组患者的血清样本通过内部酶联免疫吸附测定(ELISA)。第一组:28例原发性抗磷脂综合征(PAPS)患者(中位年龄32.5岁,范围25-34)。 12名患者有血栓形成史。 IgG / M aCL或狼疮抗凝剂(LA)或两者均为阳性。第二组:28例原因不明的孕妇(中位年龄35岁,范围23-48)。七名有血栓形成史。九名患者的IgG / M aCL阳性。该组中没有一个满足APS的札幌标准。第三组:28例系统性红斑狼疮(SLE)患者(中位年龄34岁,范围25-52)。十一名有血栓形成史。 21名患者具有IgG / M aCL和/或LA,但只有19名满足APS的札幌标准。结果:PAPS,原因不明的妊娠和SLE组的12、6和14名患者分别发现了IgA aCL。 。大多数患者将这些抗体与IgG / IgM aCL一起使用。该组中有三例妊娠原因无法解释的患者和两名SLE患者仅接受了IgA aCL。每组中一名患者存在IgAaβ2GPI。结论:尽管有IgA aCL与IgG和/或IgM aCL并存,但所有IgAaβ2GPI均与IgG和/或IgMaβ2GPI并存。 IgAaβ2GPI不能用于识别其他患有APS和妊娠率的女性。

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