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Thrombosis, Arterial and Fibrinogen

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Encyclopedia of Molecular Mechanisms of Disease
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Synonyms

A alpha polypeptide; FGA

Definition and Characteristics

Fibrinogen is a 340 kD glycoprotein of three nonidentical polypeptides linked by disulfide bonds. The promoter regions from these genes contain hepatic nuclear factor 1 and interleukin-6 responsive elements. The latter may be responsible for most of the biological variation during acute phase reactions. Thrombin causes a limited proteolysis of fibrinogen releasing fibrinopeptides A and B from the N terminal regions of the alpha and beta chains respectively. Thrombin also activates factor XIII (fibrin-stabilizing factor), which enables cross linking of fibrin molecules into a polymerized fibrin meshwork.

Prevalence

Nine and five percent of fibrinogen variability is accountable to beta chain polymorphisms detected by BclI and HaeIII, respectively [1]. The –455 A allele is present in ~20% of the population and these individuals have ~10% higher fibrinogen levels compared to those with the GG genotype [2].

Genes

Evidence...

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References

  1. Lane DA, Grant PJ (2000) Role of hemostatic gene polymorphisms in venous and arterial thrombotic disease. Blood 95:1517–32

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  2. Reiner AP, Siscovick DS, Rosendaal FR (2001) Hemostatic risk factors and arterial thrombotic disease. Thromb Haemost 85:584–95

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  3. Lim BC, Ariens RA, Carter AM, Weisel JW, Grant PJ (2003) Genetic regulation of fibrin structure and function: complex gene-environment interactions may modulate vascular risk. Lancet 361:1424–31

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  4. Kottke-Marchant K (2002) Genetic polymorphisms associated with venous and arterial thrombosis. Arch Pathol Lab Med 126:295–304

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© 2009 Springer-Verlag GmbH Berlin Heidelberg

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Cate, H.T. (2009). Thrombosis, Arterial and Fibrinogen. In: Lang, F. (eds) Encyclopedia of Molecular Mechanisms of Disease. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-29676-8_633

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