Two cases of congenital dysfibrinogenemia associated with thrombosis - Fibrinogen Praha III and Fibrinogen Plzen
Language English Country Germany Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
19718467
DOI
10.1160/th08-11-0771
PII: 08-11-0771
Knihovny.cz E-resources
- MeSH
- Platelet Aggregation MeSH
- Adult MeSH
- Fibrin chemistry MeSH
- Fibrinogen genetics MeSH
- Fibrinogens, Abnormal genetics MeSH
- Blood Coagulation MeSH
- Middle Aged MeSH
- Humans MeSH
- Microscopy, Electron, Scanning MeSH
- Mutation MeSH
- Pulmonary Embolism genetics MeSH
- Coagulation Protein Disorders complications congenital diagnosis genetics MeSH
- Thrombosis complications diagnosis genetics MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Fibrin MeSH
- Fibrinogen MeSH
- Fibrinogens, Abnormal MeSH
Congenital dysfibrinogenemia is a rare disease characterised by inherited abnormality in the fibrinogen molecule, resulting in functional defects. Two patients, a 26-year-old woman and a 61-year-old man, both with history of thrombotic events, had abnormal coagulation test results. DNA sequencing showed the heterozygous gamma Y363N mutation (Fibrinogen Praha III) and the heterozygous Aalpha N106D mutation (Fibrinogen Plzen), respectively. Fibrin polymerisation, after addition of either thrombin or reptilase, showed remarkably delayed polymerisation in both cases. Fibrinolysis experiments showed slower tPA initiated lysis of clots. SDS-PAGE did not show any difference between normal and Praha III and Plzen fibrinogens. Both mutations had a significant effect on platelet aggregation. In the presence of either ADP or TRAP, both mutations caused the decrease of platelet aggregation. SEM revealed abnormal clot morphology, with a large number of free ends and narrower fibres of both fibrin Praha III and Plzen. Praha III mutation was situated in the polymerisation pocket "a". The replacement of the bulky aromatic side chain of tyrosine by the polar uncharged small side chain of asparagine may lead to a conformational change, possibly altering the conformation of the polymerisation pocket. The Plzen mutation is situated in the coiled-coil connector and this replacement of polar uncharged asparagine residue by polar acidic aspartate changes the alpha-helical conformation of the coiled-coil connector; and may destabilise hydrogen bonds in its neighborhood. Although both mutations are situated in different regions of the molecule, both mutations have a very similar effect on fibrinogen functions and both are connected with thromboses.
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