Literature DB >> 19535131

Hereditary protein C deficiency caused by the Ala267Thr mutation in the protein C gene is associated with symptomatic and asymptomatic venous thrombosis.

Lena Tjeldhorn1, Per Morten Sandset, Kaia Haugbro, Grethe Skretting.   

Abstract

INTRODUCTION: Protein C (PC) is a key anticoagulant that regulates hemostasis, and inherited deficiency of PC is an established risk factor for venous thrombosis (VT). The factor V Leiden mutation causing activated PC (APC) resistance is an additional risk factor for VT. Reduced PC levels in the circulation and/or APC resistance do not necessarily lead to thrombotic disease. In the present study we describe and characterize an ethnic Lebanese family in which individuals with reduced PC levels and APC resistance have various clinical symptoms.
METHODS: PC activity and antigen levels and APC resistance in the family members were quantified with commercial kits. Sequencing of PC DNA and mRNA was performed with BigDye Terminator Cycle Sequencing kit on the ABI 3730 Genetic Analyzer.
RESULTS: PC antigen and anticoagulant activity in the plasma of the proband and family members ranged from 9% to 69% and 3% to 63%, respectively, compared to levels measured in pooled normal plasma. Sequencing analysis of the PC gene of family members revealed that they were either homozygous or heterozygous for the Ala267Thr mutation. In addition, three of them exhibited APC resistance. None of the family members, except the proband, have had a history of VT despite that two of them have two genetic risk factors for thrombosis. (c) 2009 Elsevier Ltd. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19535131     DOI: 10.1016/j.thromres.2009.05.013

Source DB:  PubMed          Journal:  Thromb Res        ISSN: 0049-3848            Impact factor:   3.944


  5 in total

1.  A delayed presentation of homozygous protein C deficiency in a series of children: a report on two molecular defects.

Authors:  Abdullah A Baothman; Enaam AlSobhi; Hassan A Khayat; Raed E Alsulami; Abdulaziz S Alkahtani; Abdelraheem A Al-Thobyani; Yousef I Marzouk; Mohammad A Abdelaal
Journal:  Clin Case Rep       Date:  2017-02-06

2.  A review of the diverse genetic disorders in the Lebanese population: highlighting the urgency for community genetic services.

Authors:  Ghunwa Nakouzi; Khalil Kreidieh; Soha Yazbek
Journal:  J Community Genet       Date:  2014-09-27

3.  Functional characterization of the protein C A267T mutation: evidence for impaired secretion due to defective intracellular transport.

Authors:  Lena Tjeldhorn; Nina Iversen; Kirsten Sandvig; Jonas Bergan; Per Morten Sandset; Grethe Skretting
Journal:  BMC Cell Biol       Date:  2010-09-06       Impact factor: 4.241

Review 4.  The inflammatory actions of coagulant and fibrinolytic proteases in disease.

Authors:  Michael Schuliga
Journal:  Mediators Inflamm       Date:  2015-03-24       Impact factor: 4.711

5.  The chemical chaperone sodium 4-phenylbutyrate improves the secretion of the protein CA267T mutant in CHO-K1 cells trough the GRASP55 pathway.

Authors:  Maria Eugenia Chollet; Ellen Skarpen; Nina Iversen; Per Morten Sandset; Grethe Skretting
Journal:  Cell Biosci       Date:  2015-10-09       Impact factor: 7.133

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.