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巨细胞动脉炎中的血管性血友病因子抗原与纤溶酶原激活物抑制剂

von Willebrand factor antigen and plasminogen activator inhibitor in giant cell arteritis.

作者信息

Nordborg E, Andersson R, Tengborn L, Edén S, Bengtsson B A

机构信息

Department of Rheumatology, University of Göteborg, Sweden.

出版信息

Ann Rheum Dis. 1991 May;50(5):316-20. doi: 10.1136/ard.50.5.316.

Abstract

Sixty three patients (51 women, 12 men) with giant cell arteritis were studied by serial analyses of von Willebrand factor antigen (vWF: Ag) concentration and plasminogen activator inhibitor activity. Their mean age at the time of diagnosis was 71 years. Two hundred and one randomly selected subjects from the general population, aged 75 years, served as controls. The mean concentration of vWF:Ag in the patients with giant cell arteritis before the start of corticosteroid treatment was 2.63 (SD 1.35) IU/ml compared with 1.71 (0.69) IU/ml in the general population. The vWF:Ag concentration slowly decreased and reached the control range about 18 months after the diagnosis. The vWF:Ag did not correlate with the clinical group of giant cell arteritis nor with the results of temporal artery biopsy. Flare ups and vascular complications were not indicated by the vWF:Ag. Plasminogen activator inhibitor activity in the patients was not significantly different from that of the general population at any time. It was concluded that the determination of vWF:Ag and plasminogen activator inhibitor activity is of limited clinical value in the diagnosis, prognosis, and monitoring of steroid treatment in patients with giant cell arteritis.

摘要

通过对血管性血友病因子抗原(vWF:Ag)浓度和纤溶酶原激活物抑制剂活性进行系列分析,对63例巨细胞动脉炎患者(51名女性,12名男性)进行了研究。他们诊断时的平均年龄为71岁。从普通人群中随机选取201名75岁的受试者作为对照。在开始使用皮质类固醇治疗前,巨细胞动脉炎患者的vWF:Ag平均浓度为2.63(标准差1.35)IU/ml,而普通人群为1.71(0.69)IU/ml。vWF:Ag浓度缓慢下降,在诊断后约18个月达到对照范围。vWF:Ag与巨细胞动脉炎的临床分组或颞动脉活检结果均无相关性。vWF:Ag未提示病情复发和血管并发症。患者的纤溶酶原激活物抑制剂活性在任何时候与普通人群均无显著差异。得出结论,测定vWF:Ag和纤溶酶原激活物抑制剂活性在巨细胞动脉炎患者的诊断、预后及类固醇治疗监测方面临床价值有限。

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