Literature DB >> 27766527

High prevalence of congenital thrombophilia in patients with pregnancy-related or idiopathic venous thromboembolism/pulmonary embolism.

Makoto Ikejiri1, Hideo Wada2, Norikazu Yamada3, Maki Nakamura1, Naoki Fujimoto4, Kaname Nakatani1, Akimasa Matsuda3, Yosihito Ogihara3, Takeshi Matsumoto5, Yuki Kamimoto6, Tomoaki Ikeda6, Naoyuki Katayama7, Masaaki Ito3.   

Abstract

Congenital thrombophilia which is characterized by deficiencies in proteins such as antithrombin (AT), protein C (PC) and protein S (PS), is a major cause of venous thromboembolism (VTE). A total of 130 patients with VTE were evaluated for congenital thrombophilia based on the activity of AT, PC, or PS. Fifteen VTE patients with congenital AT deficiency (11.5 %), 16 with congenital PC deficiency (12.3 %) and eight with congenital PS deficiency (6.2 %) were diagnosed using DNA analysis. The frequency of congenital AT deficiency was significantly higher in subjects with pregnancy-related and idiopathic VTE than in those with VTE due to other causes, and congenital PC and PS deficiency were frequently associated with idiopathic VTE. Among the groups examined, the plasma levels of AT were the lowest in subjects with pregnancy-related VTE. Although our findings may have been influenced by some unintentional bias, congenital thrombophilia is nevertheless a major cause of VTE in pregnant patients as well as in young or middle-aged patients without any underlying diseases.

Entities:  

Keywords:  AT; DVT; PC; PE; PS

Mesh:

Substances:

Year:  2016        PMID: 27766527     DOI: 10.1007/s12185-016-2111-2

Source DB:  PubMed          Journal:  Int J Hematol        ISSN: 0925-5710            Impact factor:   2.490


  40 in total

1.  Homozygous protein C deficiency: identification of a novel missense mutation that causes impaired secretion of the mutant protein C.

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Journal:  J Lab Clin Med       Date:  1992-06

Review 2.  Air travel and venous thromboembolism: minimizing the risk.

Authors:  John R Bartholomew; Jonathan L Schaffer; Georges F McCormick
Journal:  Cleve Clin J Med       Date:  2011-02       Impact factor: 2.321

3.  Risk of venous thromboembolism occurrence among adults with selected autoimmune diseases: a study among a U.S. cohort of commercial insurance enrollees.

Authors:  Hussain R Yusuf; W Craig Hooper; Scott D Grosse; Christopher S Parker; Sheree L Boulet; Thomas L Ortel
Journal:  Thromb Res       Date:  2014-10-22       Impact factor: 3.944

4.  Nonsynonymous mutations in three anticoagulant genes in Japanese patients with adverse pregnancy outcomes.

Authors:  Reiko Neki; Toshiyuki Miyata; Tomio Fujita; Koichi Kokame; Daisuke Fujita; Shigeyuki Isaka; Tomoaki Ikeda; Jun Yoshimatsu
Journal:  Thromb Res       Date:  2014-02-21       Impact factor: 3.944

5.  Frequent association of thrombophilia in cerebral venous sinus thrombosis.

Authors:  Makoto Ikejiri; Akihiro Shindo; Yuichiro Ii; Hidekazu Tomimoto; Norikazu Yamada; Takeshi Matsumoto; Yasunori Abe; Kaname Nakatani; Tsutomu Nobori; Hideo Wada
Journal:  Int J Hematol       Date:  2012-03       Impact factor: 2.490

6.  Symptomatic type 1 protein C deficiency caused by a de novo Ser270Leu mutation in the catalytic domain.

Authors:  B Lind; P Koefoed; S Thorsen
Journal:  Br J Haematol       Date:  2001-06       Impact factor: 6.998

7.  Protein S secretion differences of missense mutants account for phenotypic heterogeneity.

Authors:  Y Espinosa-Parrilla; T Yamazaki; N Sala; B Dahlbäck; P G de Frutos
Journal:  Blood       Date:  2000-01-01       Impact factor: 22.113

8.  Three missense mutations in the protein C heavy chain causing type I and type II protein C deficiency.

Authors:  T Miyata; Y Z Zheng; T Sakata; N Tsushima; H Kato
Journal:  Thromb Haemost       Date:  1994-01       Impact factor: 5.249

9.  Formation of a covalent disulfide-linked antithrombin-albumin complex by an antithrombin variant, antithrombin "Northwick Park".

Authors:  H Erdjument; D A Lane; H Ireland; M Panico; V Di Marzo; I Blench; H R Morris
Journal:  J Biol Chem       Date:  1987-10-05       Impact factor: 5.157

10.  Impaired secretion of the elongated mutant of protein C (protein C-Nagoya). Molecular and cellular basis for hereditary protein C deficiency.

Authors:  K Yamamoto; M Tanimoto; N Emi; T Matsushita; J Takamatsu; H Saito
Journal:  J Clin Invest       Date:  1992-12       Impact factor: 14.808

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  1 in total

1.  Update on the Clot Waveform Analysis.

Authors:  Hideo Wada; Takeshi Matsumoto; Kohshi Ohishi; Katsuya Shiraki; Motomu Shimaoka
Journal:  Clin Appl Thromb Hemost       Date:  2020 Jan-Dec       Impact factor: 2.389

  1 in total

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