Thrombophilic mutations and risk of retinal vein occlusion

Detalhes bibliográficos
Autor(a) principal: Biancardi, Ana Luiza
Data de Publicação: 2007
Outros Autores: Gadelha, Telma, Borges, Wander Inturias Sergillo, Moraes Jr., Haroldo Vieira De [UNIFESP], Spector, Nelson
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1590/S0004-27492007000600016
http://repositorio.unifesp.br/handle/11600/4005
Resumo: PURPOSE: The association of retinal vein occlusion and hereditary thrombophilia abnormalities is not established, with controversial results in the literature. This study investigates the association between retinal vein occlusion and three thrombophilic mutations: factor V 1691A (factor V Leiden), prothrombin 20210A (PT 20210A) and homozygous methylenetetrahydrofolate reductase 677T (MTHFR 677TT). METHODS: 55 consecutive retinal vein occlusion patients and 55 controls matched by age, gender and race, were tested for the presence of the following mutations: factor V Leiden, PT 20210A and MTHFR 677TT. The frequencies of the three mutations in cases and controls were compared. RESULTS: Factor V Leiden was found in 3.6% of patients and in 0% of controls; PT 20210A was found in 1.8% of patients and 3.6% of controls, (matched-pair odds ratio, 0.5; 95% confidence interval, 0.04 to 5.51); MTHFR 677TT was found in 9% of patients and 9% of controls (matched-pair odds ratio, 1; 95% confidence interval, 0.92 to 3.45). Arterial hypertension was more frequent in patients than controls (matched-pair odds ratio, 3.4; 95% confidence interval, 1.25 to 9.21). CONCLUSIONS: This study suggests that thrombophilic mutations are not risk factors for RVO. Routine investigation of hereditary thrombophilia in these patients is not justified.
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spelling Thrombophilic mutations and risk of retinal vein occlusionMutações trombofílicas e risco de oclusão venosa retinianaRetinal vein occlusionRisk factorsThrombophiliaFactor VProthrombinMethylenetetrahydrofolate reductase (NADPH2)Oclusão da veia retinianaFatores de riscoTrombofiliaFator VProtrombinaMetilenotetraidrofolato redutase (NADPH2)PURPOSE: The association of retinal vein occlusion and hereditary thrombophilia abnormalities is not established, with controversial results in the literature. This study investigates the association between retinal vein occlusion and three thrombophilic mutations: factor V 1691A (factor V Leiden), prothrombin 20210A (PT 20210A) and homozygous methylenetetrahydrofolate reductase 677T (MTHFR 677TT). METHODS: 55 consecutive retinal vein occlusion patients and 55 controls matched by age, gender and race, were tested for the presence of the following mutations: factor V Leiden, PT 20210A and MTHFR 677TT. The frequencies of the three mutations in cases and controls were compared. RESULTS: Factor V Leiden was found in 3.6% of patients and in 0% of controls; PT 20210A was found in 1.8% of patients and 3.6% of controls, (matched-pair odds ratio, 0.5; 95% confidence interval, 0.04 to 5.51); MTHFR 677TT was found in 9% of patients and 9% of controls (matched-pair odds ratio, 1; 95% confidence interval, 0.92 to 3.45). Arterial hypertension was more frequent in patients than controls (matched-pair odds ratio, 3.4; 95% confidence interval, 1.25 to 9.21). CONCLUSIONS: This study suggests that thrombophilic mutations are not risk factors for RVO. Routine investigation of hereditary thrombophilia in these patients is not justified.OBJETIVOS: A associação entre oclusão venosa retiniana e trombofilias hereditárias não está estabelecida, com resultados controversos na literatura. O presente estudo investiga a associação entre a oclusão venosa retiniana e três mutações trombofílicas: fator V 1691A (fator V Leiden), protrombina 20210A (PT 20210A) e mutação C677T do gene da metileno-tetra-hidro-folato redutase (MTHFR 677TT). MÉTODOS: Cinquenta e cinco pacientes portadores de oclusão venosa retiniana e 55 controles pareados por idade, sexo e raça foram testados para a presença das seguintes mutações: fator V Leiden, PT 20210A e MTHFR 677TT. As freqüências das três mutações em casos e controles foram comparadas. RESULTADOS: Fator V Leiden foi encontrado em 3,6% dos pacientes e em 0% dos controles; PT 20210A foi encontrada em 1.8% dos pacientes e em 3,6% dos controles, (odds ratio, 0,5; 95% IC, 0,04 to 5,51); MTHFR 677TT foi encontrada em 9% dos pacientes e em 9% dos controles (odds ratio, 1; 95% IC, 0,92 to 3,45). Hipertensão arterial foi encontrada mais freqüentemente em pacientes do que em controles (odds ratio, 3,4; 95% IC, 1,25 to 9,21). CONCLUSÕES: O presente estudo sugere que mutações trombofílicas não são fatores de risco para oclusão venosa retiniana. A investigação rotineira para trombofilias hereditárias neste grupo de pacientes não é indicada.Universidade Federal do Rio de JaneiroUFRJ Department of Internal Medicine Service of HematologyInstituto Brasileiro de OftalmologiaUniversidade Federal de São Paulo (UNIFESP)Universidade Federal do Rio de Janeiro Department of Internal MedicineUNIFESPSciELOConselho Brasileiro de OftalmologiaUniversidade Federal do Rio de JaneiroUFRJ Department of Internal Medicine Service of HematologyInstituto Brasileiro de OftalmologiaUniversidade Federal de São Paulo (UNIFESP)Universidade Federal do Rio de Janeiro Department of Internal MedicineBiancardi, Ana LuizaGadelha, TelmaBorges, Wander Inturias SergilloMoraes Jr., Haroldo Vieira De [UNIFESP]Spector, Nelson2015-06-14T13:37:12Z2015-06-14T13:37:12Z2007-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion971-974application/pdfhttp://dx.doi.org/10.1590/S0004-27492007000600016Arquivos Brasileiros de Oftalmologia. Conselho Brasileiro de Oftalmologia, v. 70, n. 6, p. 971-974, 2007.10.1590/S0004-27492007000600016S0004-27492007000600016.pdf0004-2749S0004-27492007000600016http://repositorio.unifesp.br/handle/11600/4005engArquivos Brasileiros de Oftalmologiainfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-04T18:48:24Zoai:repositorio.unifesp.br/:11600/4005Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-04T18:48:24Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Thrombophilic mutations and risk of retinal vein occlusion
Mutações trombofílicas e risco de oclusão venosa retiniana
title Thrombophilic mutations and risk of retinal vein occlusion
spellingShingle Thrombophilic mutations and risk of retinal vein occlusion
Biancardi, Ana Luiza
Retinal vein occlusion
Risk factors
Thrombophilia
Factor V
Prothrombin
Methylenetetrahydrofolate reductase (NADPH2)
Oclusão da veia retiniana
Fatores de risco
Trombofilia
Fator V
Protrombina
Metilenotetraidrofolato redutase (NADPH2)
title_short Thrombophilic mutations and risk of retinal vein occlusion
title_full Thrombophilic mutations and risk of retinal vein occlusion
title_fullStr Thrombophilic mutations and risk of retinal vein occlusion
title_full_unstemmed Thrombophilic mutations and risk of retinal vein occlusion
title_sort Thrombophilic mutations and risk of retinal vein occlusion
author Biancardi, Ana Luiza
author_facet Biancardi, Ana Luiza
Gadelha, Telma
Borges, Wander Inturias Sergillo
Moraes Jr., Haroldo Vieira De [UNIFESP]
Spector, Nelson
author_role author
author2 Gadelha, Telma
Borges, Wander Inturias Sergillo
Moraes Jr., Haroldo Vieira De [UNIFESP]
Spector, Nelson
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal do Rio de Janeiro
UFRJ Department of Internal Medicine Service of Hematology
Instituto Brasileiro de Oftalmologia
Universidade Federal de São Paulo (UNIFESP)
Universidade Federal do Rio de Janeiro Department of Internal Medicine
dc.contributor.author.fl_str_mv Biancardi, Ana Luiza
Gadelha, Telma
Borges, Wander Inturias Sergillo
Moraes Jr., Haroldo Vieira De [UNIFESP]
Spector, Nelson
dc.subject.por.fl_str_mv Retinal vein occlusion
Risk factors
Thrombophilia
Factor V
Prothrombin
Methylenetetrahydrofolate reductase (NADPH2)
Oclusão da veia retiniana
Fatores de risco
Trombofilia
Fator V
Protrombina
Metilenotetraidrofolato redutase (NADPH2)
topic Retinal vein occlusion
Risk factors
Thrombophilia
Factor V
Prothrombin
Methylenetetrahydrofolate reductase (NADPH2)
Oclusão da veia retiniana
Fatores de risco
Trombofilia
Fator V
Protrombina
Metilenotetraidrofolato redutase (NADPH2)
description PURPOSE: The association of retinal vein occlusion and hereditary thrombophilia abnormalities is not established, with controversial results in the literature. This study investigates the association between retinal vein occlusion and three thrombophilic mutations: factor V 1691A (factor V Leiden), prothrombin 20210A (PT 20210A) and homozygous methylenetetrahydrofolate reductase 677T (MTHFR 677TT). METHODS: 55 consecutive retinal vein occlusion patients and 55 controls matched by age, gender and race, were tested for the presence of the following mutations: factor V Leiden, PT 20210A and MTHFR 677TT. The frequencies of the three mutations in cases and controls were compared. RESULTS: Factor V Leiden was found in 3.6% of patients and in 0% of controls; PT 20210A was found in 1.8% of patients and 3.6% of controls, (matched-pair odds ratio, 0.5; 95% confidence interval, 0.04 to 5.51); MTHFR 677TT was found in 9% of patients and 9% of controls (matched-pair odds ratio, 1; 95% confidence interval, 0.92 to 3.45). Arterial hypertension was more frequent in patients than controls (matched-pair odds ratio, 3.4; 95% confidence interval, 1.25 to 9.21). CONCLUSIONS: This study suggests that thrombophilic mutations are not risk factors for RVO. Routine investigation of hereditary thrombophilia in these patients is not justified.
publishDate 2007
dc.date.none.fl_str_mv 2007-12-01
2015-06-14T13:37:12Z
2015-06-14T13:37:12Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1590/S0004-27492007000600016
Arquivos Brasileiros de Oftalmologia. Conselho Brasileiro de Oftalmologia, v. 70, n. 6, p. 971-974, 2007.
10.1590/S0004-27492007000600016
S0004-27492007000600016.pdf
0004-2749
S0004-27492007000600016
http://repositorio.unifesp.br/handle/11600/4005
url http://dx.doi.org/10.1590/S0004-27492007000600016
http://repositorio.unifesp.br/handle/11600/4005
identifier_str_mv Arquivos Brasileiros de Oftalmologia. Conselho Brasileiro de Oftalmologia, v. 70, n. 6, p. 971-974, 2007.
10.1590/S0004-27492007000600016
S0004-27492007000600016.pdf
0004-2749
S0004-27492007000600016
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Arquivos Brasileiros de Oftalmologia
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 971-974
application/pdf
dc.publisher.none.fl_str_mv Conselho Brasileiro de Oftalmologia
publisher.none.fl_str_mv Conselho Brasileiro de Oftalmologia
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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