Spatial Distribution of Congenital Disorders Diagnosed by the Newborn Screening Program in Ecuador

Detalhes bibliográficos
Autor(a) principal: Pozo-Palacios,Juan
Data de Publicação: 2021
Outros Autores: García-Díaz,Génesis, Cruz,Fernando, Porras,Fabián, Heras,Jessica, Cano-Pérez,Eder
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of Inborn Errors of Metabolism and Screening
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S2326-45942021000100318
Resumo: Abstract The newborn screening program in Ecuador has been operating since 2011 under the responsibility of the Ministry of Health. This program is centralized and diagnoses four diseases: congenital hypothyroidism, phenylketonuria, galactosemia, and congenital adrenal hyperplasia. This study aimed to assess the geographical distribution of newborn screening cases in Ecuador. Spatial analysis techniques were applied using the records of the National Newborn Screening Program with a congenital disease confirmed from January 2012 to December 2019. Morbidity rates per 100,000 were calculated by newborn screening disease detected and the province of birth, posteriorly, the map of its distribution was graphed and assessed using the QGIS 3.12 software. In total, 393 cases born confirmed between 2012 and 2019 were registered. The distribution of every disease tends to be different in all provinces in Ecuador; the spatial variation was significant and relative rates showed a higher incidence in some eastern provinces. In conclusion, we found a different distribution and rates of newborn screening disorders in Ecuador. The high incidence of congenital hypothyroidism, phenylketonuria, galactosemia, and congenital adrenal hyperplasia in some areas should be investigated, due could be related to ethnic, genetic, and cultural aspects of the population.
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spelling Spatial Distribution of Congenital Disorders Diagnosed by the Newborn Screening Program in Ecuadorspatial distributionnewborn screeningcongenital disordersEcuadorAbstract The newborn screening program in Ecuador has been operating since 2011 under the responsibility of the Ministry of Health. This program is centralized and diagnoses four diseases: congenital hypothyroidism, phenylketonuria, galactosemia, and congenital adrenal hyperplasia. This study aimed to assess the geographical distribution of newborn screening cases in Ecuador. Spatial analysis techniques were applied using the records of the National Newborn Screening Program with a congenital disease confirmed from January 2012 to December 2019. Morbidity rates per 100,000 were calculated by newborn screening disease detected and the province of birth, posteriorly, the map of its distribution was graphed and assessed using the QGIS 3.12 software. In total, 393 cases born confirmed between 2012 and 2019 were registered. The distribution of every disease tends to be different in all provinces in Ecuador; the spatial variation was significant and relative rates showed a higher incidence in some eastern provinces. In conclusion, we found a different distribution and rates of newborn screening disorders in Ecuador. The high incidence of congenital hypothyroidism, phenylketonuria, galactosemia, and congenital adrenal hyperplasia in some areas should be investigated, due could be related to ethnic, genetic, and cultural aspects of the population.Latin American Society Inborn Errors and Neonatal Screening (SLEIMPN); Instituto Genética para Todos (IGPT)2021-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S2326-45942021000100318Journal of Inborn Errors of Metabolism and Screening v.9 2021reponame:Journal of Inborn Errors of Metabolism and Screeninginstname:Instituto Genética para Todos (IGPT)instacron:IGPT10.1590/2326-4594-jiems-2020-0016info:eu-repo/semantics/openAccessPozo-Palacios,JuanGarcía-Díaz,GénesisCruz,FernandoPorras,FabiánHeras,JessicaCano-Pérez,Edereng2021-07-07T00:00:00Zoai:scielo:S2326-45942021000100318Revistahttp://jiems-journal.org/ONGhttps://old.scielo.br/oai/scielo-oai.phpjiems@jiems-journal.org||rgiugliani@hcpa.edu.br2326-45942326-4594opendoar:2021-07-07T00:00Journal of Inborn Errors of Metabolism and Screening - Instituto Genética para Todos (IGPT)false
dc.title.none.fl_str_mv Spatial Distribution of Congenital Disorders Diagnosed by the Newborn Screening Program in Ecuador
title Spatial Distribution of Congenital Disorders Diagnosed by the Newborn Screening Program in Ecuador
spellingShingle Spatial Distribution of Congenital Disorders Diagnosed by the Newborn Screening Program in Ecuador
Pozo-Palacios,Juan
spatial distribution
newborn screening
congenital disorders
Ecuador
title_short Spatial Distribution of Congenital Disorders Diagnosed by the Newborn Screening Program in Ecuador
title_full Spatial Distribution of Congenital Disorders Diagnosed by the Newborn Screening Program in Ecuador
title_fullStr Spatial Distribution of Congenital Disorders Diagnosed by the Newborn Screening Program in Ecuador
title_full_unstemmed Spatial Distribution of Congenital Disorders Diagnosed by the Newborn Screening Program in Ecuador
title_sort Spatial Distribution of Congenital Disorders Diagnosed by the Newborn Screening Program in Ecuador
author Pozo-Palacios,Juan
author_facet Pozo-Palacios,Juan
García-Díaz,Génesis
Cruz,Fernando
Porras,Fabián
Heras,Jessica
Cano-Pérez,Eder
author_role author
author2 García-Díaz,Génesis
Cruz,Fernando
Porras,Fabián
Heras,Jessica
Cano-Pérez,Eder
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Pozo-Palacios,Juan
García-Díaz,Génesis
Cruz,Fernando
Porras,Fabián
Heras,Jessica
Cano-Pérez,Eder
dc.subject.por.fl_str_mv spatial distribution
newborn screening
congenital disorders
Ecuador
topic spatial distribution
newborn screening
congenital disorders
Ecuador
description Abstract The newborn screening program in Ecuador has been operating since 2011 under the responsibility of the Ministry of Health. This program is centralized and diagnoses four diseases: congenital hypothyroidism, phenylketonuria, galactosemia, and congenital adrenal hyperplasia. This study aimed to assess the geographical distribution of newborn screening cases in Ecuador. Spatial analysis techniques were applied using the records of the National Newborn Screening Program with a congenital disease confirmed from January 2012 to December 2019. Morbidity rates per 100,000 were calculated by newborn screening disease detected and the province of birth, posteriorly, the map of its distribution was graphed and assessed using the QGIS 3.12 software. In total, 393 cases born confirmed between 2012 and 2019 were registered. The distribution of every disease tends to be different in all provinces in Ecuador; the spatial variation was significant and relative rates showed a higher incidence in some eastern provinces. In conclusion, we found a different distribution and rates of newborn screening disorders in Ecuador. The high incidence of congenital hypothyroidism, phenylketonuria, galactosemia, and congenital adrenal hyperplasia in some areas should be investigated, due could be related to ethnic, genetic, and cultural aspects of the population.
publishDate 2021
dc.date.none.fl_str_mv 2021-01-01
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://old.scielo.br/scielo.php?script=sci_arttext&pid=S2326-45942021000100318
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S2326-45942021000100318
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/2326-4594-jiems-2020-0016
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Latin American Society Inborn Errors and Neonatal Screening (SLEIMPN); Instituto Genética para Todos (IGPT)
publisher.none.fl_str_mv Latin American Society Inborn Errors and Neonatal Screening (SLEIMPN); Instituto Genética para Todos (IGPT)
dc.source.none.fl_str_mv Journal of Inborn Errors of Metabolism and Screening v.9 2021
reponame:Journal of Inborn Errors of Metabolism and Screening
instname:Instituto Genética para Todos (IGPT)
instacron:IGPT
instname_str Instituto Genética para Todos (IGPT)
instacron_str IGPT
institution IGPT
reponame_str Journal of Inborn Errors of Metabolism and Screening
collection Journal of Inborn Errors of Metabolism and Screening
repository.name.fl_str_mv Journal of Inborn Errors of Metabolism and Screening - Instituto Genética para Todos (IGPT)
repository.mail.fl_str_mv jiems@jiems-journal.org||rgiugliani@hcpa.edu.br
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