Dopamine D2 receptor gene polymorphisms and externalizing behaviors in children and adolescents
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , , |
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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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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1814268314673741824 |