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首页> 外文期刊>Clinical rheumatology >IgG anti-beta(2) glycoprotein I antibodies in Malaysian patients with antiphospholipid syndrome and systemic lupus erythematosus: prevalence and clinical correlations.
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IgG anti-beta(2) glycoprotein I antibodies in Malaysian patients with antiphospholipid syndrome and systemic lupus erythematosus: prevalence and clinical correlations.

机译:马来西亚抗磷脂综合症和系统性红斑狼疮患者的IgG抗β(2)糖蛋白I抗体:患病率和临床相关性。

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The aim of this study was to investigate the incidence of IgG anticardiolipin antibody (ACL) and IgG anti-beta(2) glycoprotein I antibody (anti-beta2GPI) positivity in patients with primary or secondary antiphospholipid syndrome (APS) and systemic lupus erythematosus (SLE), to assess the association between IgG ACL and anti-beta2GPI, and the relationship between the presence of ACL and anti-beta2GPI with the clinical manifestations of APS. IgG ACL and IgG anti-beta2GPI levels were measured in 51 SLE patients, 20 patients with SLE and APS (secondary APS) and 11 primary APS patients using commercially available ELISA kits. Relationships between laboratory data and clinical manifestations of the patients were examined. The incidence of IgG ACL positivity was significantly higher in primary (36.4%) and secondary (40%) APS than in SLE (13.7%) patients (P = 0.02). The incidence of IgG anti-beta2GPI positivity was significantly higher in primary (54.5%) and secondary (35%) APS than in SLE (7.8%) patients (P = 0.0006). Mean levels of IgG ACL and anti-beta2GPI were significantly higher in the primary and secondary APS than in the SLE patients (P = 0.002 for both). A significant relationship was found between IgG ACL and IgG anti-beta2GPI (P = 0.01, R(2) = 0.56). There was a significant correlation between the presence of IgG ACL and a history of thrombosis in the combined primary and secondary APS group, but not in SLE patients. In conclusion, in this study IgG ACL and IgG anti-beta2GPI are closely related and mean levels of IgG ACL and IgG anti-beta2GPI are higher in patients with either primary or secondary APS than in SLE patients.
机译:这项研究的目的是调查在原发性或继发性抗磷脂综合征(APS)和系统性红斑狼疮(APS)患者中IgG抗心磷脂抗体(ACL)和IgG抗β(2)糖蛋白I抗体(anti-beta2GPI)阳性的发生率( SLE),以评估IgG ACL和抗beta2GPI之间的关联,以及ACL和抗beta2GPI的存在与APS临床表现之间的关系。使用市售ELISA试剂盒对51例SLE患者,20例SLE和APS(继发性APS)患者和11例原发性APS患者进行了IgG ACL和IgG抗β2GPI检测。检查实验室数据与患者临床表现之间的关系。初次(36.4%)和继发(40%)APS的IgG ACL阳性发生率显着高于SLE(13.7%)患者(P = 0.02)。初次(54.5%)和继发性(35%)APS的IgG抗β2GPI阳性发生率显着高于SLE(7.8%)患者(P = 0.0006)。在原发性和继发性APS中,IgG ACL和抗β2GPI的平均水平显着高于SLE患者(两者均为P = 0.002)。发现IgG ACL和IgG抗beta2GPI之间存在显着关系(P = 0.01,R(2)= 0.56)。在合并的原发性和继发性APS组中,IgG ACL的存在与血栓形成史之间存在显着相关性,但在SLE患者中则没有。总之,在这项研究中,原发性或继发性APS患者的IgG ACL和IgG抗β2GPI密切相关,并且IgG ACL和IgG抗β2GPI的平均水平高于SLE患者。

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