Dopamine D2 receptor gene polymorphisms and externalizing behaviors in children and adolescents

Detalhes bibliográficos
Autor(a) principal: Della Torre, Osmar Henrique
Data de Publicação: 2018
Outros Autores: Paes, Lucia Arisaka, Henriques, Taciane Barbosa, Mello, Maricilda Palandi de [UNIFESP], Celeri, Eloisa Helena Rubello Valler, Dalgalarrondo, Paulo, Guerra-Junior, Gil, Santos-Junior, Amilton dos
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1186/s12881-018-0586-9
http://repositorio.unifesp.br/handle/11600/46046
Resumo: Background: Dopamine is involved in several cerebral physiological processes, and single nucleotide polymorphisms (SNP) in the dopamine D2 receptor gene (DRD2) have been associated with numerous neurological and mental disorders, including those involving alterations in cognitive and emotional processes. Methods: The aim of this study was to evaluate the association between the SNPs c.957C > T (rs6277) and c.-585A > G (rs1799978) in the DRD2 gene and behavioral characteristics of children and adolescents based on an inventory of the Child Behavior Checklist (CBCL). Children and adolescents between 8 and 20 years old who were clinically followed-up were genotyped for the SNPs c.957C > T and c.-585A > G, and related to data of the CBCL/6-18 scale assessment performed with the help of caregivers. The chi-squared test was used to assess the differences in the frequencies of the C and T alleles in the polymorphism c.957C >T and of the A and G alleles in the polymorphism c.-585A > G with respect to the grouped CBCL scores at a significance level of 5%. Multiple logistic regression models were performed, to control whether sex and/or ethnicity could influence the results. Results: Eighty-five patients were assessed overall, and the presence of the T allele (C/T and T/T) of DRD2 c.957C > T polymorphism was found to be significantly associated with the occurrence of defiant and oppositional problems and with attention and hyperactivity problems. There were no associations detected with polymorphism DRD2 c.-585A > G polymorphism. Both SNPs were in Hardy-Weinberg-equilibrium. Conclusions: Although the findings of this study are preliminary, due to its small number of participants, the presence of T allele (C/T, T/T) in c.957C > T SNP was associated with difficulty in impulse control, self-control of emotions, and conduct adjustment, which can contribute to improving the identification of mental and behavioral phenotypes associated with gene expression.
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spelling Dopamine D2 receptor gene polymorphisms and externalizing behaviors in children and adolescentsGenetic polymorphismDopamineBehaviorc.957C > T polymorphismc.-585A > G polymorphismBackground: Dopamine is involved in several cerebral physiological processes, and single nucleotide polymorphisms (SNP) in the dopamine D2 receptor gene (DRD2) have been associated with numerous neurological and mental disorders, including those involving alterations in cognitive and emotional processes. Methods: The aim of this study was to evaluate the association between the SNPs c.957C > T (rs6277) and c.-585A > G (rs1799978) in the DRD2 gene and behavioral characteristics of children and adolescents based on an inventory of the Child Behavior Checklist (CBCL). Children and adolescents between 8 and 20 years old who were clinically followed-up were genotyped for the SNPs c.957C > T and c.-585A > G, and related to data of the CBCL/6-18 scale assessment performed with the help of caregivers. The chi-squared test was used to assess the differences in the frequencies of the C and T alleles in the polymorphism c.957C >T and of the A and G alleles in the polymorphism c.-585A > G with respect to the grouped CBCL scores at a significance level of 5%. Multiple logistic regression models were performed, to control whether sex and/or ethnicity could influence the results. Results: Eighty-five patients were assessed overall, and the presence of the T allele (C/T and T/T) of DRD2 c.957C > T polymorphism was found to be significantly associated with the occurrence of defiant and oppositional problems and with attention and hyperactivity problems. There were no associations detected with polymorphism DRD2 c.-585A > G polymorphism. Both SNPs were in Hardy-Weinberg-equilibrium. Conclusions: Although the findings of this study are preliminary, due to its small number of participants, the presence of T allele (C/T, T/T) in c.957C > T SNP was associated with difficulty in impulse control, self-control of emotions, and conduct adjustment, which can contribute to improving the identification of mental and behavioral phenotypes associated with gene expression.[Della Torre, Osmar HenriquePaes, Lucia ArisakaRubello Valler Celeri, Eloisa HelenaDalgalarrondo, Paulodos Santos-Junior, Amilton] State Univ Campinas Unicamp, FCM, Dept Psychiat, Campinas, SP, Brazil[Henriques, Taciane Barbosade Mello, Maricilda Palandi] Univ Estadual Campinas, Ctr Mol Biol & Genet Engn CBMEG, Lab Human Genet, Campinas, SP, Brazil[Guerra-Junior, Gil] Univ Estadual Campinas, FCM, Ctr Invest Pediat CIPED, Growth & Dev Lab, Campinas, SP, Brazil[Guerra-Junior, Gil] Univ Estadual Campinas, FCM, Pediat Endocrinol Unit, Dept Pediat, Campinas, SP, Brazil[Della Torre, Osmar Henrique] Rua Tessalia Vieira Camargo 126, BR-13083887 Campinas, SP, BrazilUniversidade Federal de São Paulo, EPM, São Paulo, BrazilWeb of ScienceSao Paulo Research Foundation (FAPESP)FAPESP: 2012/14005-1Biomed Central Ltd2018-07-26T12:18:49Z2018-07-26T12:18:49Z2018info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion-application/pdfhttp://dx.doi.org/10.1186/s12881-018-0586-9Bmc Medical Genetics. London, v. 19, p. -, 2018.10.1186/s12881-018-0586-9WOS000431622900001.pdf1471-2350http://repositorio.unifesp.br/handle/11600/46046WOS:000431622900001enginfo:eu-repo/semantics/openAccessDella Torre, Osmar HenriquePaes, Lucia ArisakaHenriques, Taciane BarbosaMello, Maricilda Palandi de [UNIFESP]Celeri, Eloisa Helena Rubello VallerDalgalarrondo, PauloGuerra-Junior, GilSantos-Junior, Amilton dosreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-03T05:08:04Zoai:repositorio.unifesp.br/:11600/46046Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-03T05:08:04Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Dopamine D2 receptor gene polymorphisms and externalizing behaviors in children and adolescents
title Dopamine D2 receptor gene polymorphisms and externalizing behaviors in children and adolescents
spellingShingle Dopamine D2 receptor gene polymorphisms and externalizing behaviors in children and adolescents
Della Torre, Osmar Henrique
Genetic polymorphism
Dopamine
Behavior
c.957C > T polymorphism
c.-585A > G polymorphism
title_short Dopamine D2 receptor gene polymorphisms and externalizing behaviors in children and adolescents
title_full Dopamine D2 receptor gene polymorphisms and externalizing behaviors in children and adolescents
title_fullStr Dopamine D2 receptor gene polymorphisms and externalizing behaviors in children and adolescents
title_full_unstemmed Dopamine D2 receptor gene polymorphisms and externalizing behaviors in children and adolescents
title_sort Dopamine D2 receptor gene polymorphisms and externalizing behaviors in children and adolescents
author Della Torre, Osmar Henrique
author_facet Della Torre, Osmar Henrique
Paes, Lucia Arisaka
Henriques, Taciane Barbosa
Mello, Maricilda Palandi de [UNIFESP]
Celeri, Eloisa Helena Rubello Valler
Dalgalarrondo, Paulo
Guerra-Junior, Gil
Santos-Junior, Amilton dos
author_role author
author2 Paes, Lucia Arisaka
Henriques, Taciane Barbosa
Mello, Maricilda Palandi de [UNIFESP]
Celeri, Eloisa Helena Rubello Valler
Dalgalarrondo, Paulo
Guerra-Junior, Gil
Santos-Junior, Amilton dos
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Della Torre, Osmar Henrique
Paes, Lucia Arisaka
Henriques, Taciane Barbosa
Mello, Maricilda Palandi de [UNIFESP]
Celeri, Eloisa Helena Rubello Valler
Dalgalarrondo, Paulo
Guerra-Junior, Gil
Santos-Junior, Amilton dos
dc.subject.por.fl_str_mv Genetic polymorphism
Dopamine
Behavior
c.957C > T polymorphism
c.-585A > G polymorphism
topic Genetic polymorphism
Dopamine
Behavior
c.957C > T polymorphism
c.-585A > G polymorphism
description Background: Dopamine is involved in several cerebral physiological processes, and single nucleotide polymorphisms (SNP) in the dopamine D2 receptor gene (DRD2) have been associated with numerous neurological and mental disorders, including those involving alterations in cognitive and emotional processes. Methods: The aim of this study was to evaluate the association between the SNPs c.957C > T (rs6277) and c.-585A > G (rs1799978) in the DRD2 gene and behavioral characteristics of children and adolescents based on an inventory of the Child Behavior Checklist (CBCL). Children and adolescents between 8 and 20 years old who were clinically followed-up were genotyped for the SNPs c.957C > T and c.-585A > G, and related to data of the CBCL/6-18 scale assessment performed with the help of caregivers. The chi-squared test was used to assess the differences in the frequencies of the C and T alleles in the polymorphism c.957C >T and of the A and G alleles in the polymorphism c.-585A > G with respect to the grouped CBCL scores at a significance level of 5%. Multiple logistic regression models were performed, to control whether sex and/or ethnicity could influence the results. Results: Eighty-five patients were assessed overall, and the presence of the T allele (C/T and T/T) of DRD2 c.957C > T polymorphism was found to be significantly associated with the occurrence of defiant and oppositional problems and with attention and hyperactivity problems. There were no associations detected with polymorphism DRD2 c.-585A > G polymorphism. Both SNPs were in Hardy-Weinberg-equilibrium. Conclusions: Although the findings of this study are preliminary, due to its small number of participants, the presence of T allele (C/T, T/T) in c.957C > T SNP was associated with difficulty in impulse control, self-control of emotions, and conduct adjustment, which can contribute to improving the identification of mental and behavioral phenotypes associated with gene expression.
publishDate 2018
dc.date.none.fl_str_mv 2018-07-26T12:18:49Z
2018-07-26T12:18:49Z
2018
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/10.1186/s12881-018-0586-9
Bmc Medical Genetics. London, v. 19, p. -, 2018.
10.1186/s12881-018-0586-9
WOS000431622900001.pdf
1471-2350
http://repositorio.unifesp.br/handle/11600/46046
WOS:000431622900001
url http://dx.doi.org/10.1186/s12881-018-0586-9
http://repositorio.unifesp.br/handle/11600/46046
identifier_str_mv Bmc Medical Genetics. London, v. 19, p. -, 2018.
10.1186/s12881-018-0586-9
WOS000431622900001.pdf
1471-2350
WOS:000431622900001
dc.language.iso.fl_str_mv eng
language eng
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv -
application/pdf
dc.publisher.none.fl_str_mv Biomed Central Ltd
publisher.none.fl_str_mv Biomed Central Ltd
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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