首页> 美国卫生研究院文献>The Journal of Neurology and Psychopathology >Anticardiolipin antibodies in patients with multiple sclerosis do not represent a subgroup of patients according to clinical familial and biological characteristics
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Anticardiolipin antibodies in patients with multiple sclerosis do not represent a subgroup of patients according to clinical familial and biological characteristics

机译:根据临床家族和生物学特征多发性硬化症患者中的抗心磷脂抗体不代表患者亚组

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摘要

Objectives: To determine whether patients with MS who are positive for aCL Ab have specific characteristics. Methods: 285 consecutive patients with MS were tested for aCL Ab positivity. Patients also underwent complete autoimmune screening and were systematically evaluated for clinical characteristics and individual or family history of autoimmune disease. Results: aCL Ab positivity was found in 42 patients (15%). The main isotype was aCL IgM (32 patients, 11%). Demographics and clinical characteristics including sex, age at onset, course of the disease, expanded disability status scale score, and progression index were not different between aCL Ab positive and aCL Ab negative patients. Clinical systems involved at onset or during the course of the disease were not different from what is usually observed in MS. aCL Ab positivity was not associated with an increased frequency of autoimmune disease and was not predictive of a family history of autoimmune disease. Patients positive for aCL IgM were more frequently positive for the presence of non-organ specific antibodies (53% v 39%, respectively, p = 0.02). Conclusions: These results do not support the hypothesis that patients with MS with aCL Ab constitute a subgroup of MS according to demographic clinical and familial characteristics. The greater frequency of other antibodies in aCL Ab positive patients suggests that they only reflect a more general autoimmune activation in MS.
机译:目的:确定aCL Ab阳性的MS患者是否具有特定特征。方法:连续285例MS患者接受了aCL Ab阳性检测。还对患者进行了完整的自身免疫检查,并系统评估了自身免疫疾病的临床特征和个人或家族史。结果:42例患者(15%)发现aCL Ab阳性。主要同种型是aCL IgM(32例患者,占11%)。 aCL Ab阳性和aCL Ab阴性患者的人口统计学和临床​​特征,包括性别,发病年龄,病程,残疾状况扩大量表评分和进展指数均无差异。发病或病程中涉及的临床系统与MS中通常观察到的没有什么不同。 aCL抗体阳性与自身免疫性疾病发生率增加无关,也不能预测自身免疫性疾病家族史。对于aCL IgM呈阳性的患者,其非器官特异性抗体的阳性率更高(分别为53%对39%,p = 0.02)。结论:这些结果不支持以下假设:根据人口统计学临床和家族特征,患有aCL Ab的MS患者属于MS亚组。 aCL Ab阳性患者中其他抗体的出现频率较高,表明它们仅反映了MS中更普遍的自身免疫激活。

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