Thrombophilic mutations and risk of retinal vein occlusion
Autor(a) principal: | |
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Data de Publicação: | 2007 |
Outros Autores: | , , , |
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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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 |
_version_ |
1814268364969738240 |