Prevalence of Chromosomal Abnormalities in Spontaneous Abortions or Fetal Deaths

Detalhes bibliográficos
Autor(a) principal: Bastos, Raquel
Data de Publicação: 2014
Outros Autores: Ramalho, Carla, Dória, Sofia
Tipo de documento: Artigo
Idioma: por
eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/3952
Resumo: Introduction: Spontaneous abortion is one of the most frequent problems of pregnancy, estimated to affect, at least, one in every four women who tries to conceive. The main purpose of this work was to study the prevalence of chromosomal abnormalities in gestational losses, evaluating their relation with maternal age, gestational age and previous abortion history.Material and Methods: Retrospective study of 401 pregnancy loss cases that have gone through cytogenetic and anatomopathologic analysis between January 2008 and June 2012, in Centro Hospitalar de S. João, Oporto.Results: Of the 401 cases sent to cytogenetic study, it was possible to obtain information about the chromosomal complement in 333 cases, of which 72.7% showed normal karyotype, and 27.3% abnormal karyotype. Aneuploidies represented 92.3% of the identified chromosomopathies, with trisomies being the most frequent, related with an advanced maternal age and an early gestational age. There was no agreement between the results of the cytogenetic and the anatomopathologic analysis.Discussion/Conclusion: The prevalence of chromosomal abnormalities, during the first trimester, is similar between sporadic and recurrent miscarriages. With increased maternal age, trisomies, the most frequent type of aneuploidy, are more likely to occur, with a mean increment in probability of 7.4% per year. A significant karyotype-pathological correlation was not established. Maternal contamination is the main obstacle to the accurate determination of the prevalence of chromosomal abnormalities. The molecular cytogenetic techniques already available can overcome the limitations of the conventional technique.
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spelling Prevalence of Chromosomal Abnormalities in Spontaneous Abortions or Fetal DeathsEstudo da Prevalência de Anomalias Cromossómicas em Abortamentos Espontâneos ou Mortes FetaisIntroduction: Spontaneous abortion is one of the most frequent problems of pregnancy, estimated to affect, at least, one in every four women who tries to conceive. The main purpose of this work was to study the prevalence of chromosomal abnormalities in gestational losses, evaluating their relation with maternal age, gestational age and previous abortion history.Material and Methods: Retrospective study of 401 pregnancy loss cases that have gone through cytogenetic and anatomopathologic analysis between January 2008 and June 2012, in Centro Hospitalar de S. João, Oporto.Results: Of the 401 cases sent to cytogenetic study, it was possible to obtain information about the chromosomal complement in 333 cases, of which 72.7% showed normal karyotype, and 27.3% abnormal karyotype. Aneuploidies represented 92.3% of the identified chromosomopathies, with trisomies being the most frequent, related with an advanced maternal age and an early gestational age. There was no agreement between the results of the cytogenetic and the anatomopathologic analysis.Discussion/Conclusion: The prevalence of chromosomal abnormalities, during the first trimester, is similar between sporadic and recurrent miscarriages. With increased maternal age, trisomies, the most frequent type of aneuploidy, are more likely to occur, with a mean increment in probability of 7.4% per year. A significant karyotype-pathological correlation was not established. Maternal contamination is the main obstacle to the accurate determination of the prevalence of chromosomal abnormalities. The molecular cytogenetic techniques already available can overcome the limitations of the conventional technique.Introdução: O abortamento espontâneo é um dos problemas mais frequentes da gravidez, estimando-se que afete, pelo menos, 25% das mulheres que tentam engravidar. O objetivo principal deste trabalho foi o estudo da prevalência das anomalias cromossómicas em perdas gestacionais, analisando a sua relação com a idade materna, idade gestacional e história de abortamentos prévios.Material e Métodos: Realizou-se um estudo retrospetivo em 401 casos de perdas de gravidez que efetuaram análise citogenética e anátomo-patológica, entre janeiro de 2008 e junho de 2012, no Centro Hospitalar de S. João.Resultados: Dos 401 casos enviados para estudo citogenético foi possível obter informação sobre o complemento cromossómico em 333 casos, dos quais 72,7% apresentaram cariótipo normal e 27,3% cariótipo anormal. As aneuploidias representaram 92,3% das cromossomopatias identificadas, sendo as trissomias as mais frequentes, associadas a uma idade materna avançada e a uma idade gestacional precoce. Não se verificou concordância entre os resultados da análise anátomo-patológica e citogenética.Discussão e Conclusão: A prevalência de anomalias cromossómicas, no primeiro trimestre, foi semelhante entre os casos de abortamento esporádico e recorrente. Com o aumento da idade materna observou-se um aumento das trissomias, com um incremento médio de 7,4% no risco de ocorrência por ano. Não foi estabelecida uma correlação cariótipo-patológica significativa. A contaminação materna da amostra foi o principal entrave à determinação exata da prevalência de anomalias cromossómicas. As técnicas de citogenética molecular já disponíveis podem colmatar esta e outras limitações da técnica convencional.Ordem dos Médicos2014-01-08info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfapplication/pdfhttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/3952oai:ojs.www.actamedicaportuguesa.com:article/3952Acta Médica Portuguesa; Vol. 27 No. 1 (2014): January-February; 42-48Acta Médica Portuguesa; Vol. 27 N.º 1 (2014): Janeiro-Fevereiro; 42-481646-07580870-399Xreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPporenghttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/3952https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/3952/3877https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/3952/3958Bastos, RaquelRamalho, CarlaDória, Sofiainfo:eu-repo/semantics/openAccess2022-12-20T11:03:09Zoai:ojs.www.actamedicaportuguesa.com:article/3952Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:18:39.780209Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Prevalence of Chromosomal Abnormalities in Spontaneous Abortions or Fetal Deaths
Estudo da Prevalência de Anomalias Cromossómicas em Abortamentos Espontâneos ou Mortes Fetais
title Prevalence of Chromosomal Abnormalities in Spontaneous Abortions or Fetal Deaths
spellingShingle Prevalence of Chromosomal Abnormalities in Spontaneous Abortions or Fetal Deaths
Bastos, Raquel
title_short Prevalence of Chromosomal Abnormalities in Spontaneous Abortions or Fetal Deaths
title_full Prevalence of Chromosomal Abnormalities in Spontaneous Abortions or Fetal Deaths
title_fullStr Prevalence of Chromosomal Abnormalities in Spontaneous Abortions or Fetal Deaths
title_full_unstemmed Prevalence of Chromosomal Abnormalities in Spontaneous Abortions or Fetal Deaths
title_sort Prevalence of Chromosomal Abnormalities in Spontaneous Abortions or Fetal Deaths
author Bastos, Raquel
author_facet Bastos, Raquel
Ramalho, Carla
Dória, Sofia
author_role author
author2 Ramalho, Carla
Dória, Sofia
author2_role author
author
dc.contributor.author.fl_str_mv Bastos, Raquel
Ramalho, Carla
Dória, Sofia
description Introduction: Spontaneous abortion is one of the most frequent problems of pregnancy, estimated to affect, at least, one in every four women who tries to conceive. The main purpose of this work was to study the prevalence of chromosomal abnormalities in gestational losses, evaluating their relation with maternal age, gestational age and previous abortion history.Material and Methods: Retrospective study of 401 pregnancy loss cases that have gone through cytogenetic and anatomopathologic analysis between January 2008 and June 2012, in Centro Hospitalar de S. João, Oporto.Results: Of the 401 cases sent to cytogenetic study, it was possible to obtain information about the chromosomal complement in 333 cases, of which 72.7% showed normal karyotype, and 27.3% abnormal karyotype. Aneuploidies represented 92.3% of the identified chromosomopathies, with trisomies being the most frequent, related with an advanced maternal age and an early gestational age. There was no agreement between the results of the cytogenetic and the anatomopathologic analysis.Discussion/Conclusion: The prevalence of chromosomal abnormalities, during the first trimester, is similar between sporadic and recurrent miscarriages. With increased maternal age, trisomies, the most frequent type of aneuploidy, are more likely to occur, with a mean increment in probability of 7.4% per year. A significant karyotype-pathological correlation was not established. Maternal contamination is the main obstacle to the accurate determination of the prevalence of chromosomal abnormalities. The molecular cytogenetic techniques already available can overcome the limitations of the conventional technique.
publishDate 2014
dc.date.none.fl_str_mv 2014-01-08
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dc.publisher.none.fl_str_mv Ordem dos Médicos
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dc.source.none.fl_str_mv Acta Médica Portuguesa; Vol. 27 No. 1 (2014): January-February; 42-48
Acta Médica Portuguesa; Vol. 27 N.º 1 (2014): Janeiro-Fevereiro; 42-48
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