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蛋白Z依赖性蛋白酶抑制剂基因内的突变与静脉血栓栓塞性疾病相关:一种新的易栓症形式。

Mutations within the protein Z-dependent protease inhibitor gene are associated with venous thromboembolic disease: a new form of thrombophilia.

作者信息

Van de Water Neil, Tan Tina, Ashton Fern, O'Grady Anna, Day Tony, Browett Peter, Ockelford Paul, Harper Paul

机构信息

Department of Haematology, Auckland Hospital, Auckland, New Zealand.

出版信息

Br J Haematol. 2004 Oct;127(2):190-4. doi: 10.1111/j.1365-2141.2004.05189.x.

Abstract

Protein Z-dependent protease inhibitor (ZPI) is a serpin that inhibits the activated coagulation factors X and XI. The precise physiological significance of ZPI in the control of haemostasis is unknown although a deficiency of ZPI may be predicted to alter this balance. The coding region of the ZPI gene was screened for mutations using denaturing high-performance liquid chromatography. 16 mutations/polymorphisms within the coding region of ZPI were identified including two mutations, which generated stop codons at residues R67 and W303. We observed nonsense mutations within the ZPI gene in 4.4% of thrombosis patients (n = 250) compared with 0.8% of controls (n = 250). The difference in distribution of stop codon mutations between thrombosis patients and controls was significant (P = 0.02) with an odds ratio of 5.7 (95% confidence interval, 1.25-26.0). Our results suggest an association between ZPI deficiency and venous thrombosis and we propose that ZPI deficiency is potentially a new form of thrombophilia.

摘要

蛋白Z依赖性蛋白酶抑制剂(ZPI)是一种丝氨酸蛋白酶抑制剂,可抑制活化的凝血因子X和XI。尽管预计ZPI缺乏可能会改变这种平衡,但其在止血控制中的精确生理意义尚不清楚。使用变性高效液相色谱法筛选ZPI基因的编码区突变。在ZPI编码区内鉴定出16个突变/多态性,其中包括两个突变,它们在R67和W303残基处产生了终止密码子。我们在4.4%的血栓形成患者(n = 250)中观察到ZPI基因内的无义突变,而对照组(n = 250)中这一比例为0.8%。血栓形成患者和对照组之间终止密码子突变分布的差异具有统计学意义(P = 0.02),优势比为5.7(95%置信区间,1.25 - 26.0)。我们的结果表明ZPI缺乏与静脉血栓形成之间存在关联,并且我们提出ZPI缺乏可能是一种新的易栓症形式。

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