Cargando…
Association of fibrinogen and plasmin inhibitor, but not coagulation factor XIII gene polymorphisms with coronary artery disease
BACKGROUND: In the final phase of clot formation, fibrinogen constitutes frame, whereas factor XIII (FXIII) active form is responsible for the covalent cross-linking of fibrin fibres and plasmin inhibitor (PI), thus contributing to clot stability. It could be expected that any change of coagulation...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society of Medical Biochemists of Serbia, Belgrade
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7982289/ https://www.ncbi.nlm.nih.gov/pubmed/33776563 http://dx.doi.org/10.5937/jomb0-26839 |
_version_ | 1783667690023419904 |
---|---|
author | Bronić, Ana Ferenčak, Goran Bernat, Robert Leniček-Krleža, Jasna Dumić, Jerka Dabelić, Sanja |
author_facet | Bronić, Ana Ferenčak, Goran Bernat, Robert Leniček-Krleža, Jasna Dumić, Jerka Dabelić, Sanja |
author_sort | Bronić, Ana |
collection | PubMed |
description | BACKGROUND: In the final phase of clot formation, fibrinogen constitutes frame, whereas factor XIII (FXIII) active form is responsible for the covalent cross-linking of fibrin fibres and plasmin inhibitor (PI), thus contributing to clot stability. It could be expected that any change of coagulation factors' structure affects the clot formation and modulates the atherothrombotic risk. The aim was to determine the frequency of four single nucleotide polymorphisms: (i) A > G in codon 312 of the fibrinogen α-chain gene (rs6050, Thr312AlaFGA), (ii) C > T at position 10034 of the 3 - untranslated region in the fibrinogen γ-chain gene (rs2066865, 10034C > T FGG), (iii) C > T in codon 564 of the FXIII-A subunit gene (rs5982, Pro564LeuFXIII-A), and (iv) C > T in codon 6 of the plasmin inhibitor gene (rs2070863, Arg6TrpPI) in Croatian patients and their association with coronary artery disease (CAD). METHODS: We performed the unrelated case-control association study on the consecutive sample of patients 18 years old, who had undergone coronary angiography for investigation of chest pain and suspected CAD. The cases were patients with confirmed CAD (N=201), and the controls were the subjects with no CAD (N=119). Samples were genotyped using PCR-RFLP analysis. RESULTS: Observed frequencies of the rare alleles of Thr312Ala FGA, 10034C > T FGG, Leu564Pro FXIII-A and Arg6Trp PI polymorphisms were 21%, 17%, 14%, 20%, respectively. Patients with 10034C > T FGG CC genotype had 3.5 times (95% CI 1.02-12.03) higher adjusted odds for CAD than patients with 10034C > T FGG TT genotype. Patients with Arg6Trp PI CC genotype had 3.86 times (95% CI 1.23-12.12) higher odds for CAD than patients with Arg6Trp PI TT genotype. It seems that those genotype-related higher odds are also male-gender related. No difference was observed regarding any other investigated polymorphism. CONCLUSIONS: Our finding suggests that 10034C > T FGG and Arg6Trp PI are associated with CAD. |
format | Online Article Text |
id | pubmed-7982289 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Society of Medical Biochemists of Serbia, Belgrade |
record_format | MEDLINE/PubMed |
spelling | pubmed-79822892021-03-26 Association of fibrinogen and plasmin inhibitor, but not coagulation factor XIII gene polymorphisms with coronary artery disease Bronić, Ana Ferenčak, Goran Bernat, Robert Leniček-Krleža, Jasna Dumić, Jerka Dabelić, Sanja J Med Biochem Original Paper BACKGROUND: In the final phase of clot formation, fibrinogen constitutes frame, whereas factor XIII (FXIII) active form is responsible for the covalent cross-linking of fibrin fibres and plasmin inhibitor (PI), thus contributing to clot stability. It could be expected that any change of coagulation factors' structure affects the clot formation and modulates the atherothrombotic risk. The aim was to determine the frequency of four single nucleotide polymorphisms: (i) A > G in codon 312 of the fibrinogen α-chain gene (rs6050, Thr312AlaFGA), (ii) C > T at position 10034 of the 3 - untranslated region in the fibrinogen γ-chain gene (rs2066865, 10034C > T FGG), (iii) C > T in codon 564 of the FXIII-A subunit gene (rs5982, Pro564LeuFXIII-A), and (iv) C > T in codon 6 of the plasmin inhibitor gene (rs2070863, Arg6TrpPI) in Croatian patients and their association with coronary artery disease (CAD). METHODS: We performed the unrelated case-control association study on the consecutive sample of patients 18 years old, who had undergone coronary angiography for investigation of chest pain and suspected CAD. The cases were patients with confirmed CAD (N=201), and the controls were the subjects with no CAD (N=119). Samples were genotyped using PCR-RFLP analysis. RESULTS: Observed frequencies of the rare alleles of Thr312Ala FGA, 10034C > T FGG, Leu564Pro FXIII-A and Arg6Trp PI polymorphisms were 21%, 17%, 14%, 20%, respectively. Patients with 10034C > T FGG CC genotype had 3.5 times (95% CI 1.02-12.03) higher adjusted odds for CAD than patients with 10034C > T FGG TT genotype. Patients with Arg6Trp PI CC genotype had 3.86 times (95% CI 1.23-12.12) higher odds for CAD than patients with Arg6Trp PI TT genotype. It seems that those genotype-related higher odds are also male-gender related. No difference was observed regarding any other investigated polymorphism. CONCLUSIONS: Our finding suggests that 10034C > T FGG and Arg6Trp PI are associated with CAD. Society of Medical Biochemists of Serbia, Belgrade 2021-03-12 2021-03-12 /pmc/articles/PMC7982289/ /pubmed/33776563 http://dx.doi.org/10.5937/jomb0-26839 Text en 2021 Ana Bronić, Goran Ferenčak, Robert Bernat, Jasna Leniček-Krleža, Jerka Dumić, Sanja Dabelić, published by CEON/CEES http://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 License. |
spellingShingle | Original Paper Bronić, Ana Ferenčak, Goran Bernat, Robert Leniček-Krleža, Jasna Dumić, Jerka Dabelić, Sanja Association of fibrinogen and plasmin inhibitor, but not coagulation factor XIII gene polymorphisms with coronary artery disease |
title | Association of fibrinogen and plasmin inhibitor, but not coagulation factor XIII gene polymorphisms with coronary artery disease |
title_full | Association of fibrinogen and plasmin inhibitor, but not coagulation factor XIII gene polymorphisms with coronary artery disease |
title_fullStr | Association of fibrinogen and plasmin inhibitor, but not coagulation factor XIII gene polymorphisms with coronary artery disease |
title_full_unstemmed | Association of fibrinogen and plasmin inhibitor, but not coagulation factor XIII gene polymorphisms with coronary artery disease |
title_short | Association of fibrinogen and plasmin inhibitor, but not coagulation factor XIII gene polymorphisms with coronary artery disease |
title_sort | association of fibrinogen and plasmin inhibitor, but not coagulation factor xiii gene polymorphisms with coronary artery disease |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7982289/ https://www.ncbi.nlm.nih.gov/pubmed/33776563 http://dx.doi.org/10.5937/jomb0-26839 |
work_keys_str_mv | AT bronicana associationoffibrinogenandplasmininhibitorbutnotcoagulationfactorxiiigenepolymorphismswithcoronaryarterydisease AT ferencakgoran associationoffibrinogenandplasmininhibitorbutnotcoagulationfactorxiiigenepolymorphismswithcoronaryarterydisease AT bernatrobert associationoffibrinogenandplasmininhibitorbutnotcoagulationfactorxiiigenepolymorphismswithcoronaryarterydisease AT lenicekkrlezajasna associationoffibrinogenandplasmininhibitorbutnotcoagulationfactorxiiigenepolymorphismswithcoronaryarterydisease AT dumicjerka associationoffibrinogenandplasmininhibitorbutnotcoagulationfactorxiiigenepolymorphismswithcoronaryarterydisease AT dabelicsanja associationoffibrinogenandplasmininhibitorbutnotcoagulationfactorxiiigenepolymorphismswithcoronaryarterydisease |