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一种用于疟疾中因子 VII 缺乏底物制备及凝血研究的新方法。

A new method for factor VII deficient substrate preparation and coagulation studies in malaria.

作者信息

Rojanasthien S, Surakamollert V, Isarangkura P, Boonpucknavig S

机构信息

Hematology Division, Ramathibodi Hospital, Faculty of Medicine, Mahidol University, Bangkok, Thailand.

出版信息

Southeast Asian J Trop Med Public Health. 1993;24 Suppl 1:225-8.

PMID:7886582
Abstract

A simplified technique using DEAE-cellulose chromatography for the preparation of factor VII deficient substrate was developed in order to reduce the high cost of individual factor VII assay in the routine coagulation laboratory. The substrate prepared from cryo-removed human and bovine plasma had a high correlation (r = 0.9929) with two of the most popular imported commercial substrates available (DADE, Ortho). When compared several other imported commercial substrates of equal quality, the prepared substrate was 3,000 to 6,000 times cheaper. Using the prepared factor VII deficient substrate along with other commercial substrates available, two hundred and fifty patients with malaria (fifty cases of P. vivax and two hundred cases of P. falciparum) were studied for coagulation and fibrinolysis abnormalities. Only P. falciparum infections showed prolonged PT and aPTT which correlated with the degree of parasitemia (r = 0.0972). Factors V, VII, and IX were the most sensitive parameters in the expression of coagulation defects and most coagulation abnormalities were due to liver involvement. Plasmin activity was normal in P. vivax patients but it was significantly increased in P. falciparum patients with > 5% parasitemia. Only two of the complicated cases of P. falciparum patients showed the evidence of DIC.

摘要

为降低常规凝血实验室中单个因子 VII 检测的高昂成本,开发了一种使用二乙氨基乙基纤维素色谱法制备因子 VII 缺乏底物的简化技术。从去除冷沉淀的人血浆和牛血浆制备的底物与两种最常用的进口商业底物(达德、奥索)具有高度相关性(r = 0.9929)。与其他几种质量相当的进口商业底物相比,制备的底物便宜 3000 至 6000 倍。使用制备的因子 VII 缺乏底物以及其他可用的商业底物,对 250 例疟疾患者(50 例间日疟原虫和 200 例恶性疟原虫)进行了凝血和纤维蛋白溶解异常研究。仅恶性疟原虫感染显示凝血酶原时间(PT)和活化部分凝血活酶时间(aPTT)延长,且与寄生虫血症程度相关(r = 0.0972)。因子 V、VII 和 IX 是凝血缺陷表达中最敏感的参数,大多数凝血异常是由于肝脏受累。间日疟原虫患者的纤溶酶活性正常,但在寄生虫血症>5%的恶性疟原虫患者中显著升高。仅两例恶性疟原虫复杂病例显示有弥散性血管内凝血(DIC)证据。

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