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Morphology and Progression in Primary Varicose Vein Disorder Due to 677C>T and 1298A>C Variants of MTHFR

BACKGROUND: Clinical assessment and prognostic stratification of primary varicose veins have remained controversial and the molecular pathogenesis is unknown. Previous data have suggested a contribution of the MTHFR (methylenetetrahydrofolate reductase) polymorphism c.677C>T. METHODS: We collecte...

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Autores principales: Wilmanns, Christoph, Cooper, Alexis, Wockner, Leesa, Katsandris, Sotirios, Glaser, Nadine, Meyer, Alexander, Bartsch, Oliver, Binder, Harald, Walter, Paul Karl, Zechner, Ulrich
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4484817/
https://www.ncbi.nlm.nih.gov/pubmed/26137554
http://dx.doi.org/10.1016/j.ebiom.2015.01.006
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author Wilmanns, Christoph
Cooper, Alexis
Wockner, Leesa
Katsandris, Sotirios
Glaser, Nadine
Meyer, Alexander
Bartsch, Oliver
Binder, Harald
Walter, Paul Karl
Zechner, Ulrich
author_facet Wilmanns, Christoph
Cooper, Alexis
Wockner, Leesa
Katsandris, Sotirios
Glaser, Nadine
Meyer, Alexander
Bartsch, Oliver
Binder, Harald
Walter, Paul Karl
Zechner, Ulrich
author_sort Wilmanns, Christoph
collection PubMed
description BACKGROUND: Clinical assessment and prognostic stratification of primary varicose veins have remained controversial and the molecular pathogenesis is unknown. Previous data have suggested a contribution of the MTHFR (methylenetetrahydrofolate reductase) polymorphism c.677C>T. METHODS: We collected blood and vein specimens from 159 consecutive patients undergoing varicose vein surgery, or autologous vein reconstruction for arterial occlusive disease as controls. We compared the frequencies of c.677C>T and another polymorphism of MTHFR, c.1298A>C, with morphology and types of complicated disease. Morphology was recorded as a trunk or perforator type and peripheral congestive complication was defined as chronic venous insufficiency (CEAP C3–6) associated with edema and skin manifestations. FINDINGS: Multivariate analysis of genotypes for c.677C>T and c.1298A>C indicated that c.677C>T was associated significantly with the trunk phenotype (43/53 patients, 81%, p < 0.01), while c.1298A>C was associated significantly with the perforator phenotype (18/24 patients, 75%, p < 0.01) of primary varicose veins. Accordingly, when both c.677C>T and c.1298A>C displayed a heterozygous genotype, the patients were more likely to present with both phenotypes. Additionally, c.1298A>C was found to be strongly linked to the congestive complication (34/51 patients, 67%, p < 0.01). INTERPRETATION: Both polymorphisms of MTHFR may be involved in the morphological specification of primary varicose veins and contribute to the development of complicated disease. FUNDING: None.
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spelling pubmed-44848172015-07-01 Morphology and Progression in Primary Varicose Vein Disorder Due to 677C>T and 1298A>C Variants of MTHFR Wilmanns, Christoph Cooper, Alexis Wockner, Leesa Katsandris, Sotirios Glaser, Nadine Meyer, Alexander Bartsch, Oliver Binder, Harald Walter, Paul Karl Zechner, Ulrich EBioMedicine Original Article BACKGROUND: Clinical assessment and prognostic stratification of primary varicose veins have remained controversial and the molecular pathogenesis is unknown. Previous data have suggested a contribution of the MTHFR (methylenetetrahydrofolate reductase) polymorphism c.677C>T. METHODS: We collected blood and vein specimens from 159 consecutive patients undergoing varicose vein surgery, or autologous vein reconstruction for arterial occlusive disease as controls. We compared the frequencies of c.677C>T and another polymorphism of MTHFR, c.1298A>C, with morphology and types of complicated disease. Morphology was recorded as a trunk or perforator type and peripheral congestive complication was defined as chronic venous insufficiency (CEAP C3–6) associated with edema and skin manifestations. FINDINGS: Multivariate analysis of genotypes for c.677C>T and c.1298A>C indicated that c.677C>T was associated significantly with the trunk phenotype (43/53 patients, 81%, p < 0.01), while c.1298A>C was associated significantly with the perforator phenotype (18/24 patients, 75%, p < 0.01) of primary varicose veins. Accordingly, when both c.677C>T and c.1298A>C displayed a heterozygous genotype, the patients were more likely to present with both phenotypes. Additionally, c.1298A>C was found to be strongly linked to the congestive complication (34/51 patients, 67%, p < 0.01). INTERPRETATION: Both polymorphisms of MTHFR may be involved in the morphological specification of primary varicose veins and contribute to the development of complicated disease. FUNDING: None. Elsevier 2015-01-15 /pmc/articles/PMC4484817/ /pubmed/26137554 http://dx.doi.org/10.1016/j.ebiom.2015.01.006 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Wilmanns, Christoph
Cooper, Alexis
Wockner, Leesa
Katsandris, Sotirios
Glaser, Nadine
Meyer, Alexander
Bartsch, Oliver
Binder, Harald
Walter, Paul Karl
Zechner, Ulrich
Morphology and Progression in Primary Varicose Vein Disorder Due to 677C>T and 1298A>C Variants of MTHFR
title Morphology and Progression in Primary Varicose Vein Disorder Due to 677C>T and 1298A>C Variants of MTHFR
title_full Morphology and Progression in Primary Varicose Vein Disorder Due to 677C>T and 1298A>C Variants of MTHFR
title_fullStr Morphology and Progression in Primary Varicose Vein Disorder Due to 677C>T and 1298A>C Variants of MTHFR
title_full_unstemmed Morphology and Progression in Primary Varicose Vein Disorder Due to 677C>T and 1298A>C Variants of MTHFR
title_short Morphology and Progression in Primary Varicose Vein Disorder Due to 677C>T and 1298A>C Variants of MTHFR
title_sort morphology and progression in primary varicose vein disorder due to 677c>t and 1298a>c variants of mthfr
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4484817/
https://www.ncbi.nlm.nih.gov/pubmed/26137554
http://dx.doi.org/10.1016/j.ebiom.2015.01.006
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