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开始口服抗凝治疗后不久,蛋白C抗原减少并形成异常蛋白。

Decrease in protein C antigen and formation of an abnormal protein soon after starting oral anticoagulant therapy.

作者信息

Viganò S, Mannucci P M, Solinas S, Bottasso B, Mariani G

出版信息

Br J Haematol. 1984 Jun;57(2):213-20.

PMID:6547348
Abstract

Changes in protein C antigen (PC:Ag) have been compared with those in factor II, VII, IX and X antigens (II:Ag; VII:Ag; IX:Ag and X:Ag) in 10 patients starting on oral anticoagulant therapy with warfarin, monitored with thrombotest. Between days 0 and 3 of therapy, PC:Ag decreased at the same rate as VII:Ag, whilst IX:Ag, X:Ag and II:Ag decreased at progressively slower rates. On days 15 and 21, clotting proteins and PC:Ag did not differ significantly. Before and after warfarin, PC:Ag had the same mobility on crossed immunoelectrophoresis in Ca2+-free agarose gel; with Ca2+, a protein with faster anodal mobility appeared on day 1 and became maximal 5 d after warfarin was started. These findings indicate that the rate of PC decrease is closer to that of factor VII than those of factors IX, X and II, and that an abnormal PC with poor Ca2+-binding properties appears soon after treatment is started. The early decrease in the physiological inactivator (i.e. PC) might contribute to the poor antithrombotic efficacy of anticoagulant therapy during the first days.

摘要

在10例开始使用华法林进行口服抗凝治疗并采用凝血试验监测的患者中,对蛋白C抗原(PC:Ag)的变化与凝血因子II、VII、IX和X抗原(II:Ag;VII:Ag;IX:Ag和X:Ag)的变化进行了比较。在治疗的第0天至第3天之间,PC:Ag与VII:Ag以相同的速率下降,而IX:Ag、X:Ag和II:Ag下降的速率逐渐减慢。在第15天和第21天,凝血蛋白和PC:Ag没有显著差异。在使用华法林前后,PC:Ag在无钙琼脂糖凝胶的交叉免疫电泳中具有相同的迁移率;在有钙的情况下,一种具有更快阳极迁移率的蛋白质在第1天出现,并在开始使用华法林后5天达到最大值。这些发现表明,PC下降的速率比因子IX、X和II更接近因子VII,并且在开始治疗后不久就会出现一种钙结合特性较差的异常PC。生理性灭活剂(即PC)的早期下降可能导致抗凝治疗最初几天的抗血栓疗效不佳。

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