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Search for mutations in the genes for coagulation factors V and VIII with a possible predisposition to activated protein C resistance.

作者信息

Bokarewa M I, Falk G, Bremme K, Blombäck M, Wiman B

机构信息

Department of Clinical Chemistry/Blood Coagulation Research, Karolinska Hospital, Stockholm, Sweden.

出版信息

Eur J Clin Invest. 1997 Apr;27(4):340-5. doi: 10.1046/j.1365-2362.1997.1180660.x.

DOI:10.1046/j.1365-2362.1997.1180660.x
PMID:9134384
Abstract

A total of 74 non-pregnant women with a previous episode of thrombosis were investigated for activated protein C (APC) resistance in the aPTT-based and factor IXa-X-based assays and for the presence of mutations in all APC-cleavage sites in the heavy chains of factor V and factor VIII. DNA fragments were amplified with the polymerase chain reaction (PCR) and those encoding for the Arg-306 and Arg-506 (factor V) and for Arg-740 (factor VIII) cleavage sites were subjected to restriction enzyme analysis. DNA fragments of 29 selected patients corresponding to the Arg-306 and Arg-679 cleavage sites in factor V, and to the Arg-336 and Arg-562 cleavage sites in factor VIII were sequenced. APC resistance was found in 40 cases, using the aPTT-based assay and in 35, using the factor IXa-X-based assay (23 patients were APC resistant in both assays), whereas 22 individuals had a normal response to APC. Forty-three patients carried Arg-506 to Gln mutation in factor V. No other polymorphism or mutation was found in the genes for factors V or VIII in the vicinity of the APC cleavage sites. It was concluded that the difference in response to APC in the two assays may not be explained by the presence of mutations in the APC cleavage sites of factor V and factor VIII in this group of patients. The data do not exclude the presence of mutations elsewhere in the factor V or factor VIII genes.

摘要

相似文献

1
Search for mutations in the genes for coagulation factors V and VIII with a possible predisposition to activated protein C resistance.
Eur J Clin Invest. 1997 Apr;27(4):340-5. doi: 10.1046/j.1365-2362.1997.1180660.x.
2
Influence of factor VIII/von Willebrand complex on the activated protein C-resistance phenotype and on the risk for venous thromboembolism in heterozygous carriers of the factor V Leiden mutation.凝血因子VIII/血管性血友病因子复合物对凝血因子V莱顿突变杂合子携带者活化蛋白C抵抗表型及静脉血栓栓塞风险的影响。
Blood Coagul Fibrinolysis. 1999 Oct;10(7):409-16.
3
A chromogenic assay for activated protein C resistance.活化蛋白C抵抗的显色测定法。
Br J Haematol. 1995 Aug;90(4):884-91. doi: 10.1111/j.1365-2141.1995.tb05210.x.
4
Cleavage of factor V at Arg 506 by activated protein C and the expression of anticoagulant activity of factor V.活化蛋白C对因子V在精氨酸506处的切割及因子V抗凝活性的表达。
Blood. 1999 Apr 15;93(8):2552-8.
5
Molecular mechanisms of activated protein C resistance. Properties of factor V isolated from an individual with homozygosity for the Arg506 to Gln mutation in the factor V gene.活化蛋白C抵抗的分子机制。从因子V基因中存在精氨酸506突变为谷氨酰胺纯合子的个体中分离出的因子V的特性。
Biochem J. 1996 Jan 15;313 ( Pt 2)(Pt 2):467-72. doi: 10.1042/bj3130467.
6
Inherited resistance to activated protein C, a major cause of venous thrombosis, is due to a mutation in the factor V gene.遗传性活化蛋白C抵抗是静脉血栓形成的主要原因,它是由凝血因子V基因的突变引起的。
Haemostasis. 1994 Mar-Apr;24(2):139-51. doi: 10.1159/000217094.
7
Absence of mutations at the activated protein C cleavage sites of factor VIII in 125 patients with venous thrombosis.125例静脉血栓形成患者中因子VIII活化蛋白C裂解位点无突变。
Br J Haematol. 1996 Mar;92(3):740-3. doi: 10.1046/j.1365-2141.1996.349885.x.
8
Factor Va is inactivated by activated protein C in the absence of cleavage sites at Arg-306, Arg-506, and Arg-679.在精氨酸-306、精氨酸-506和精氨酸-679处不存在切割位点的情况下,凝血因子Va会被活化蛋白C灭活。
J Biol Chem. 2004 Feb 20;279(8):6567-75. doi: 10.1074/jbc.M308574200. Epub 2003 Dec 2.
9
Coagulation assay with improved specificity to factor V mutants insensitive to activated protein C.对活化蛋白C不敏感的因子V突变体具有更高特异性的凝血测定法。
Thromb Res. 1995 Nov 1;80(3):255-64. doi: 10.1016/0049-3848(95)00174-p.
10
Resistance to activated protein C (APC): mutation at Arg506 of coagulation factor V and vascular access thrombosis in haemodialysis patients.对活化蛋白C(APC)的抵抗:凝血因子V的精氨酸506突变与血液透析患者的血管通路血栓形成
Nephrol Dial Transplant. 1996 Apr;11(4):668-72. doi: 10.1093/oxfordjournals.ndt.a027357.

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