Literature DB >> 28503122

Thrombosis in Inherited Fibrinogen Disorders.

Wolfgang Korte1, Man-Chiu Poon2, Alfonso Iorio3, Michael Makris4,5.   

Abstract

Although inherited fibrinogen disorders (IFD) are primarily considered to be bleeding disorders, they are associated with a higher thrombotic complication risk than defects in other clotting factors. Managing IFD patients with thrombosis is challenging as anticoagulant treatment may exacerbate the underlying bleeding risk which can be life-threatening. Due to the low prevalence of IFD, there is little information on pathophysiology or optimal treatment of thrombosis in these patients. We searched the literature for cases of thrombosis among IFD patients and identified a total of 128 patient reports. In approximately half of the cases, thromboses were spontaneous, while in the others trauma, surgery, and parturition contributed to the risk. The true mechanism(s) of thrombosis in IFD patients remain to be elucidated. A variety of anticoagulant treatments have been used in the treatment or prevention of thrombosis, sometimes with concurrent fibrinogen replacement therapy. There is no definite evidence that fibrinogen supplementation increases the risk of thrombosis, and it may potentially be effective in the treatment and prevention of both thrombosis and hemorrhage in IFD patients.

Entities:  

Keywords:  Blood coagulation disorders; Congenital; Fibrinogen; Hemorrhage; Inherited; Thrombosis

Year:  2017        PMID: 28503122      PMCID: PMC5425758          DOI: 10.1159/000452864

Source DB:  PubMed          Journal:  Transfus Med Hemother        ISSN: 1660-3796            Impact factor:   3.747


  93 in total

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Review 2.  Fibrin(ogen) and thrombotic disease.

Authors:  R A S Ariëns
Journal:  J Thromb Haemost       Date:  2013-06       Impact factor: 5.824

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Journal:  Arterioscler Thromb Vasc Biol       Date:  1996-05       Impact factor: 8.311

4.  Hypofibrinogenaemia and massive thrombosis.

Authors:  I M Nilsson; J E Niléhn; S Cronberg; G Nordén
Journal:  Acta Med Scand       Date:  1966-07

Review 5.  Fibrinogen replacement therapy for congenital fibrinogen deficiency.

Authors:  L Bornikova; F Peyvandi; G Allen; J Bernstein; M J Manco-Johnson
Journal:  J Thromb Haemost       Date:  2011-09       Impact factor: 5.824

6.  Thrombophilic dysfibrinogen Tokyo V with the amino acid substitution of gammaAla327Thr: formation of fragile but fibrinolysis-resistant fibrin clots and its relevance to arterial thromboembolism.

Authors:  Akiei Hamano; Jun Mimuro; Motonori Aoshima; Takeyoshi Itoh; Noboru Kitamura; Susumu Nishinarita; Katsuhiro Takano; Akira Ishiwata; Yuji Kashiwakura; Kazuki Niwa; Tomoko Ono; Seiji Madoiwa; Teruko Sugo; Michio Matsuda; Yoichi Sakata
Journal:  Blood       Date:  2004-01-08       Impact factor: 22.113

7.  Increased prothrombin activation in a patient with congenital afibrinogenemia is reversible by fibrinogen substitution.

Authors:  W Korte; A Feldges
Journal:  Clin Investig       Date:  1994-05

8.  Hereditary dysfibrinogenemia in a patient with thrombotic disease.

Authors:  N Carrell; D A Gabriel; P M Blatt; M E Carr; J McDonagh
Journal:  Blood       Date:  1983-08       Impact factor: 22.113

9.  Afibrinogenaemia: a rare cause of young myocardial infarct.

Authors:  N Kumar; R Padma Kumar; B Ramesh; N Garg
Journal:  Singapore Med J       Date:  2008-04       Impact factor: 1.858

Review 10.  Thromboembolism in patients with congenital afibrinogenaemia. Long-term observational data and systematic review.

Authors:  Michael Nagler; Johanna A Kremer Hovinga; Lorenzo Alberio; Kristiina Peter-Salonen; Hendrik von Tengg-Kobligk; Daniel Lottaz; Marguerite Neerman-Arbez; Bernhard Lämmle
Journal:  Thromb Haemost       Date:  2016-07-07       Impact factor: 5.249

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  20 in total

1.  Identification of mutations in SLC4A1, GP1BA and HFE in a family with venous thrombosis of unknown cause by next-generation sequencing.

Authors:  Wei-An Chang; Chau-Chyun Sheu; Kuan-Ting Liu; Jheng-Heng Shen; Meng-Chi Yen; Po-Lin Kuo
Journal:  Exp Ther Med       Date:  2018-09-04       Impact factor: 2.447

Review 2.  Rare thrombophilic conditions.

Authors:  Gian Luca Salvagno; Chiara Pavan; Giuseppe Lippi
Journal:  Ann Transl Med       Date:  2018-09

3.  Congenital dysfibrinogenaemia presented with preterm premature rupture of the membranes and vaginal bleeding.

Authors:  Zaker I Schwabkey; Farrell C Sheehan; Courtney Bellomo; Mihir Raval
Journal:  BMJ Case Rep       Date:  2020-09-18

4.  Identification of Two Novel Fibrinogen Bβ Chain Mutations in Two Slovak Families with Quantitative Fibrinogen Disorders.

Authors:  Tomas Simurda; Jana Zolkova; Zuzana Snahnicanova; Dusan Loderer; Ingrid Skornova; Juraj Sokol; Jan Hudecek; Jan Stasko; Zora Lasabova; Peter Kubisz
Journal:  Int J Mol Sci       Date:  2017-12-29       Impact factor: 5.923

5.  Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population.

Authors:  Arshi Naz; Arijit Biswas; Tehmina Nafees Khan; Anne Goodeve; Nisar Ahmed; Nazish Saqlain; Shariq Ahmed; Ikram Din Ujjan; Tahir S Shamsi; Johannes Oldenburg
Journal:  Thromb J       Date:  2017-09-12

Review 6.  Clinical Consequences and Molecular Bases of Low Fibrinogen Levels.

Authors:  Marguerite Neerman-Arbez; Alessandro Casini
Journal:  Int J Mol Sci       Date:  2018-01-08       Impact factor: 5.923

Review 7.  Genetic Variants in the FGB and FGG Genes Mapping in the Beta and Gamma Nodules of the Fibrinogen Molecule in Congenital Quantitative Fibrinogen Disorders Associated with a Thrombotic Phenotype.

Authors:  Tomas Simurda; Monika Brunclikova; Rosanna Asselta; Sonia Caccia; Jana Zolkova; Zuzana Kolkova; Dusan Loderer; Ingrid Skornova; Jan Hudecek; Zora Lasabova; Jan Stasko; Peter Kubisz
Journal:  Int J Mol Sci       Date:  2020-06-29       Impact factor: 5.923

Review 8.  Fibrinolysis and Inflammation in Venous Thrombus Resolution.

Authors:  Subhradip Mukhopadhyay; Tierra A Johnson; Nadire Duru; Marguerite S Buzza; Nisha R Pawar; Rajabrata Sarkar; Toni M Antalis
Journal:  Front Immunol       Date:  2019-06-14       Impact factor: 7.561

9.  A Chinese family with congenital Dysfibrinogenemia carries a heterozygous missense mutation in FGA: Concerning the genetic abnormality and clinical treatment.

Authors:  Jihao Zhou; Peng Zhu; Xinyou Zhang
Journal:  Pak J Med Sci       Date:  2017 Jul-Aug       Impact factor: 1.088

10.  A Novel Mutation in the Fibrinogen Bβ Chain (c.490G>A; End of Exon 3) Causes a Splicing Abnormality and Ultimately Leads to Congenital Hypofibrinogenemia.

Authors:  Chiaki Taira; Kazuyuki Matsuda; Shinpei Arai; Mitsutoshi Sugano; Takeshi Uehara; Nobuo Okumura
Journal:  Int J Mol Sci       Date:  2017-11-20       Impact factor: 5.923

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