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Extra-criteria manifestations of antiphospholipid syndrome: Risk assessment and management

机译:抗磷脂综合征的额外标准表现:风险评估和管理

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ObjectivesExtra-criteria manifestations of antiphospholipid syndrome (APS) might impact on prognosis and morbidity of the disease. In this study, we aimed to evaluate a population of patients with primary APS (PAPS) whether the extra-criteria manifestations were more frequently found in subjects with higher adjusted Global APS Score (aGAPSS) values when compared to patients with thrombotic and/or obstetric APS (“criteria” manifestations) only. MethodsClinical records were analyzed to retrieve extra-criteria manifestation of APS, cardiovascular risk factors and antiphospholipid antibodies profile. The aGAPSS was calculated by adding the points, as follows: 3 for hyperlipidaemia, 1 for arterial hypertension, 5 for anticardiolipin antibodies IgG/IgM, 4 for anti-β2 glycoprotein I IgG/IgM, and 4 for lupus anticoagulant. ResultsThis retrospective multicenter study included 89 consecutive PAPS [mean age 43.1 (S.D. ± 12.9), female 67%, 52% arterial and 65% venous]. Twenty-seven patients (30.3%) had a history of livedo, 19 (21.3%) had a history of confirmed thrombocytopenia, 3 (3.4%) had biopsy-proven antiphospholipid antibodies (aPL)-related nephropathy and 3 (3.4%) had a history of valvulopathy. Patients with extra-criteria manifestations presented a mean aGAPSS significantly higher [mean 10.30 (S.D. ± 3.57, range: 4–17) vs mean 8.16 (S.D. ± 3.52;range: 4–16,p= 0.005). When comparing patients with and without extra-criteria manifestations, the first group had significantly higher incidence of anti-β2GPI antibodies positivity (59% and 33%, respectively,p= 0.015), double aPL positivities (53% and 31%, respectively,p= 0.034), cerebrovascular events history (52% and 24%, respectively,p= 0.007) and arterial hypertension (52% and 24%, respectively,p= 0.007). ConclusionsOur results suggest that patients with higher aGAPSS, might be at higher risk for developing extra-criteria manifestations of APS and should therefore undergo a thorough laboratory and instrumental evaluation.
机译:抗磷脂综合征(APS)的客观XTRA标准可能影响疾病的预后和发病率。在这项研究中,我们旨在评估初级APS(PAPS)患者患者患者是否在具有较高调整后的全球APS评分(AGAPSS)值的受试者中更常见的标准表现,与血栓形成和/或产科患者相比APS(“标准”表现形式)。分析了方法临床记录以检测AP,心血管危险因素和抗磷脂抗体谱的额外标准表现。通过添加点来计算agapss,如下:3用于高脂血症,1用于动脉高血压,5用于抗真磷脂抗体IgG / IgM,4用于抗β2糖蛋白I IgG / IgM,4,用于狼疮抗凝血剂4。结果Strsthis回顾性多中心研究包括89个连续的PAP [平均年龄43.1(S.D.±12.9),女67%,52%的动脉和65%的静脉]。二十七名患者(30.3%)历史,19(21.3%)有确诊的血小板减少症的历史,3(3.4%)有活检证明的抗磷脂抗体(APL)相关的肾病和3(3.4%) valvulopathy的历史。标准表现出的患者显着提高了平均值[平均10.30(S.D.±3.57,范围:4-17)VS平均值8.16(S.D.±3.52;范围:4-16,P = 0.005)。在将患者与无额外标准表现进行比较时,第一组的抗-β2GPi抗体阳性的发病率显着更高(分别为59%和33%,P = 0.015),分别是双APL正皮(53%和31%, P = 0.034),脑血管事件史(分别为52%和24%,P = 0.007)和动脉高压(分别为52%和24%,P = 0.007)。结论您的结果表明,患有更高的患者,可能存在较高的风险,以发展APS的额外标准表现,因此应该接受彻底的实验室和工具评估。

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