Relation between genetic polymorphism and broncopulmonary dysplasia: a narrative review

Detalhes bibliográficos
Autor(a) principal: Santos Neto, Teobaldo Ivo dos
Data de Publicação: 2022
Outros Autores: Garcia, Bianca Portela, Sousa, Icaro Araújo de, Nobrega Neto, Antônio de Pádua Rocha, Araujo, Thiago de Souza Lopes, Souza, Luan Kelves Miranda de
Tipo de documento: Artigo
Idioma: por
Título da fonte: Research, Society and Development
Texto Completo: https://rsdjournal.org/index.php/rsd/article/view/32037
Resumo: Genetic polymorphisms are characterized by variation in specific DNA sequences, with the presence of two or more variant forms in more than 1% of the population. The presence of polymorphisms does not always determine the development of a disease, however, they can influence risk factors associated with diseases, such as bronchopulmonary dysplasia (BPD). BPD is a chronic neonatal lung disease characterized by a need to implement oxygen as well as ventilatory support in the first 28 days of life. Because it is multifactorial, both the early diagnosis and the treatment of BPD is difficult, the study of genetic polymorphisms associated with BPD can be useful for identifying molecular targets that can be used to prevent or treat BPD. The aim of this study was to carry out a narrative review about the relationship between genetic polymorphisms and the development of bronchopulmonary dysplasia. A search was performed in the VHL, PubMed and Scielo databases using the descriptors: “bronchopulmonary dysplasia”, “genetic polymorphism” and “premature newborn”. After using filters, abstracts and text of the articles, 26 articles were selected for this study. Although knowledge about the pathogenesis of BPD has increased significantly in recent years, not all mechanisms that lead to lung damage are fully understood, which explains the search for new therapeutic approaches, such as cell therapy, use of natural antioxidants that have been shown to be effective in preliminary studies. In this review, we demonstrate nine polymorphisms that are related to an increased risk of developing BPD in preterm infants.
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spelling Relation between genetic polymorphism and broncopulmonary dysplasia: a narrative reviewRelación entre polimorfismo genético y displasia broncopulmonar: una revisión narrativaRelação entre polimorfismos genéticos e displasia broncopulmonar: uma revisão narrativa Displasia broncopulmonarPolimorfismo genéticoRecém-nascido prematuro.Displasia broncopulmonarPolimorfismo genéticoRecién nacido prematuro.Bronchopulmonary dysplasiaGenetic polymorphismPremature newborn.Genetic polymorphisms are characterized by variation in specific DNA sequences, with the presence of two or more variant forms in more than 1% of the population. The presence of polymorphisms does not always determine the development of a disease, however, they can influence risk factors associated with diseases, such as bronchopulmonary dysplasia (BPD). BPD is a chronic neonatal lung disease characterized by a need to implement oxygen as well as ventilatory support in the first 28 days of life. Because it is multifactorial, both the early diagnosis and the treatment of BPD is difficult, the study of genetic polymorphisms associated with BPD can be useful for identifying molecular targets that can be used to prevent or treat BPD. The aim of this study was to carry out a narrative review about the relationship between genetic polymorphisms and the development of bronchopulmonary dysplasia. A search was performed in the VHL, PubMed and Scielo databases using the descriptors: “bronchopulmonary dysplasia”, “genetic polymorphism” and “premature newborn”. After using filters, abstracts and text of the articles, 26 articles were selected for this study. Although knowledge about the pathogenesis of BPD has increased significantly in recent years, not all mechanisms that lead to lung damage are fully understood, which explains the search for new therapeutic approaches, such as cell therapy, use of natural antioxidants that have been shown to be effective in preliminary studies. In this review, we demonstrate nine polymorphisms that are related to an increased risk of developing BPD in preterm infants.Los polimorfismos genéticos se caracterizan por la variación en secuencias específicas de ADN, con la presencia de dos o más formas variantes en más del 1% de la población. La presencia de polimorfismos no siempre determina el desarrollo de una enfermedad, sin embargo, pueden influir en factores de riesgo asociados a enfermedades, como la displasia broncopulmonar (DBP). La DBP es una enfermedad pulmonar neonatal crónica caracterizada por la necesidad de implementar oxígeno y soporte ventilatorio en los primeros 28 días de vida. Debido a que es multifactorial, tanto el diagnóstico precoz como el tratamiento del TLP es difícil, el estudio de los polimorfismos genéticos asociados al TLP puede ser útil para identificar dianas moleculares que puedan utilizarse para prevenir o tratar el TLP. El objetivo de este estudio fue realizar una revisión narrativa sobre la relación entre los polimorfismos genéticos y el desarrollo de displasia broncopulmonar. Se realizó una búsqueda en las bases de datos de la BVS, PubMed y Scielo utilizando los descriptores: “displasia broncopulmonar”, “polimorfismo genético” y “recién nacido prematuro”. Después de utilizar filtros, resúmenes y texto de los artículos, se seleccionaron 26 artículos para este estudio. Aunque el conocimiento sobre la patogenia de la DBP ha aumentado significativamente en los últimos años, no se conocen por completo todos los mecanismos que conducen al daño pulmonar, lo que explica la búsqueda de nuevos enfoques terapéuticos, como la terapia celular, el uso de antioxidantes naturales que han demostrado ser eficaz en los estudios preliminares. En esta revisión, demostramos nueve polimorfismos que están relacionados con un mayor riesgo de desarrollar BPD en bebés prematuros.Polimorfismos genéticos são caracterizados pela variação em sequências específicas de DNA, com a presença de duas ou mais formas variantes em mais de 1% da população. A presença de polimorfismos nem sempre determina o desenvolvimento de uma doença, entretanto, podem influenciar em fatores de risco associados a doenças, como a displasia broncopulmonar (DBP). A DBP é uma doença pulmonar crônica neonatal é caracterizada por uma necessidade de implementação de oxigênio, bem como um suporte ventilatório em nos primeiros 28 dias de vida. Por ser multifatorial, tanto o diagnóstico precoce como o tratamento da DBP é dificultado, o estudo dos polimorfismos genéticos associados à DBP pode ser útil para identificação de alvos moleculares que poderão ser usados para prevenir ou tratar a DBP. O objetivo deste estudo foi realizar uma revisão narrativa acerca da relação entre polimorfismos genéticos e o desenvolvimento de displasia broncopulmonar. Foi realizada uma busca nas bases de dados BVS, PubMed e Scielo utilizando os descritores: “displasia broncopulmonar”, “polimorfismo genético” e “recém-nascido prematuro”. Após a utilização de filtros, resumos e texto dos artigos, selecionou-se 26 artigos para este estudo. Embora o conhecimento sobre a patogênese da DBP tenha aumentado significativamente nos últimos anos, nem todos os mecanismos que levam ao dano pulmonar são completamente compreendidos, explicando a busca por novas abordagens terapêuticas, tais como terapia celular, uso de antioxidantes naturais que têm se mostrado eficazes em estudos preliminaries. Nesta revisão, demonstramos nove polimorfismos que estão relacionados ao aumento do risco de desenvolvimento de DBP por recém-nascidos prematuros.Research, Society and Development2022-07-12info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/3203710.33448/rsd-v11i9.32037Research, Society and Development; Vol. 11 No. 9; e35311932037Research, Society and Development; Vol. 11 Núm. 9; e35311932037Research, Society and Development; v. 11 n. 9; e353119320372525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIporhttps://rsdjournal.org/index.php/rsd/article/view/32037/27210Copyright (c) 2022 Teobaldo Ivo dos Santos Neto; Bianca Portela Garcia; Icaro Araújo de Sousa; Antônio de Pádua Rocha Nobrega Neto; Thiago de Souza Lopes Araujo; Luan Kelves Miranda de Souzahttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessSantos Neto, Teobaldo Ivo dos Garcia, Bianca Portela Sousa, Icaro Araújo de Nobrega Neto, Antônio de Pádua Rocha Araujo, Thiago de Souza Lopes Souza, Luan Kelves Miranda de 2022-07-21T12:36:16Zoai:ojs.pkp.sfu.ca:article/32037Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2024-01-17T09:48:10.029960Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false
dc.title.none.fl_str_mv Relation between genetic polymorphism and broncopulmonary dysplasia: a narrative review
Relación entre polimorfismo genético y displasia broncopulmonar: una revisión narrativa
Relação entre polimorfismos genéticos e displasia broncopulmonar: uma revisão narrativa
title Relation between genetic polymorphism and broncopulmonary dysplasia: a narrative review
spellingShingle Relation between genetic polymorphism and broncopulmonary dysplasia: a narrative review
Santos Neto, Teobaldo Ivo dos
Displasia broncopulmonar
Polimorfismo genético
Recém-nascido prematuro.
Displasia broncopulmonar
Polimorfismo genético
Recién nacido prematuro.
Bronchopulmonary dysplasia
Genetic polymorphism
Premature newborn.
title_short Relation between genetic polymorphism and broncopulmonary dysplasia: a narrative review
title_full Relation between genetic polymorphism and broncopulmonary dysplasia: a narrative review
title_fullStr Relation between genetic polymorphism and broncopulmonary dysplasia: a narrative review
title_full_unstemmed Relation between genetic polymorphism and broncopulmonary dysplasia: a narrative review
title_sort Relation between genetic polymorphism and broncopulmonary dysplasia: a narrative review
author Santos Neto, Teobaldo Ivo dos
author_facet Santos Neto, Teobaldo Ivo dos
Garcia, Bianca Portela
Sousa, Icaro Araújo de
Nobrega Neto, Antônio de Pádua Rocha
Araujo, Thiago de Souza Lopes
Souza, Luan Kelves Miranda de
author_role author
author2 Garcia, Bianca Portela
Sousa, Icaro Araújo de
Nobrega Neto, Antônio de Pádua Rocha
Araujo, Thiago de Souza Lopes
Souza, Luan Kelves Miranda de
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Santos Neto, Teobaldo Ivo dos
Garcia, Bianca Portela
Sousa, Icaro Araújo de
Nobrega Neto, Antônio de Pádua Rocha
Araujo, Thiago de Souza Lopes
Souza, Luan Kelves Miranda de
dc.subject.por.fl_str_mv Displasia broncopulmonar
Polimorfismo genético
Recém-nascido prematuro.
Displasia broncopulmonar
Polimorfismo genético
Recién nacido prematuro.
Bronchopulmonary dysplasia
Genetic polymorphism
Premature newborn.
topic Displasia broncopulmonar
Polimorfismo genético
Recém-nascido prematuro.
Displasia broncopulmonar
Polimorfismo genético
Recién nacido prematuro.
Bronchopulmonary dysplasia
Genetic polymorphism
Premature newborn.
description Genetic polymorphisms are characterized by variation in specific DNA sequences, with the presence of two or more variant forms in more than 1% of the population. The presence of polymorphisms does not always determine the development of a disease, however, they can influence risk factors associated with diseases, such as bronchopulmonary dysplasia (BPD). BPD is a chronic neonatal lung disease characterized by a need to implement oxygen as well as ventilatory support in the first 28 days of life. Because it is multifactorial, both the early diagnosis and the treatment of BPD is difficult, the study of genetic polymorphisms associated with BPD can be useful for identifying molecular targets that can be used to prevent or treat BPD. The aim of this study was to carry out a narrative review about the relationship between genetic polymorphisms and the development of bronchopulmonary dysplasia. A search was performed in the VHL, PubMed and Scielo databases using the descriptors: “bronchopulmonary dysplasia”, “genetic polymorphism” and “premature newborn”. After using filters, abstracts and text of the articles, 26 articles were selected for this study. Although knowledge about the pathogenesis of BPD has increased significantly in recent years, not all mechanisms that lead to lung damage are fully understood, which explains the search for new therapeutic approaches, such as cell therapy, use of natural antioxidants that have been shown to be effective in preliminary studies. In this review, we demonstrate nine polymorphisms that are related to an increased risk of developing BPD in preterm infants.
publishDate 2022
dc.date.none.fl_str_mv 2022-07-12
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dc.identifier.uri.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/32037
10.33448/rsd-v11i9.32037
url https://rsdjournal.org/index.php/rsd/article/view/32037
identifier_str_mv 10.33448/rsd-v11i9.32037
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/32037/27210
dc.rights.driver.fl_str_mv https://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Research, Society and Development
publisher.none.fl_str_mv Research, Society and Development
dc.source.none.fl_str_mv Research, Society and Development; Vol. 11 No. 9; e35311932037
Research, Society and Development; Vol. 11 Núm. 9; e35311932037
Research, Society and Development; v. 11 n. 9; e35311932037
2525-3409
reponame:Research, Society and Development
instname:Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
instname_str Universidade Federal de Itajubá (UNIFEI)
instacron_str UNIFEI
institution UNIFEI
reponame_str Research, Society and Development
collection Research, Society and Development
repository.name.fl_str_mv Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)
repository.mail.fl_str_mv rsd.articles@gmail.com
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