DRD4 genotyping may differentiate symptoms of attention-deficit/hyperactivity disorder and sluggish cognitive tempo

Detalhes bibliográficos
Autor(a) principal: Bolat, Hilmi
Data de Publicação: 2020
Outros Autores: Ercan, Eyüp Sabri, Bolat, Gül Ünsel, Tahillioğlu, Akın, Yazici, Kemal Utku, Bacanli, Ali, Pariltay, Erhan, Jafari, Duygu Aygüneş, Kosova, Buket, Özgül, Semiha, Rohde, Luis Augusto Paim, Akin, Haluk
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/230710
Resumo: Objective: Studies to reduce the heterogeneity of attention-deficit/hyperactivity disorder (ADHD) have increased interest in the concept of sluggish cognitive tempo (SCT). The aim of this study was to investigate if the prevalence of two variable-number tandem repeats (VNTRs) located within the 30 -untranslated region of the DAT1 gene and in exon 3 of the dopamine D4 receptor (DRD4) gene differ among four groups (31 subjects with SCT but no ADHD, 146 individuals with ADHD but no SCT, 67 subjects with SCT + ADHD, and 92 healthy controls). Methods: We compared the sociodemographic profiles, neurocognitive domains, and prevalence of two VNTRs in SCT and ADHD subjects versus typically developing (TD) controls. Results: The SCT without ADHD group had a higher proportion of females and lower parental educational attainment. Subjects in this group performed worse on neuropsychological tests, except for psychomotor speed and commission errors, compared to controls. However, the ADHD without SCT group performed significantly worse on all neuropsychological domains than controls. We found that 4R homozygosity for the DRD4 gene was most prevalent in the ADHD without SCT group. The SCT without ADHD group had the highest 7R allele frequency, differing significantly from the ADHD without SCT group. Conclusion: The 7R allele of DRD4 gene was found to be significantly more prevalent in SCT cases than in ADHD cases. No substantial neuropsychological differences were found between SCT and ADHD subjects.
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spelling Bolat, HilmiErcan, Eyüp SabriBolat, Gül ÜnselTahillioğlu, AkınYazici, Kemal UtkuBacanli, AliPariltay, ErhanJafari, Duygu AygüneşKosova, BuketÖzgül, SemihaRohde, Luis Augusto PaimAkin, Haluk2021-10-14T04:30:44Z20201516-4446http://hdl.handle.net/10183/230710001131600Objective: Studies to reduce the heterogeneity of attention-deficit/hyperactivity disorder (ADHD) have increased interest in the concept of sluggish cognitive tempo (SCT). The aim of this study was to investigate if the prevalence of two variable-number tandem repeats (VNTRs) located within the 30 -untranslated region of the DAT1 gene and in exon 3 of the dopamine D4 receptor (DRD4) gene differ among four groups (31 subjects with SCT but no ADHD, 146 individuals with ADHD but no SCT, 67 subjects with SCT + ADHD, and 92 healthy controls). Methods: We compared the sociodemographic profiles, neurocognitive domains, and prevalence of two VNTRs in SCT and ADHD subjects versus typically developing (TD) controls. Results: The SCT without ADHD group had a higher proportion of females and lower parental educational attainment. Subjects in this group performed worse on neuropsychological tests, except for psychomotor speed and commission errors, compared to controls. However, the ADHD without SCT group performed significantly worse on all neuropsychological domains than controls. We found that 4R homozygosity for the DRD4 gene was most prevalent in the ADHD without SCT group. The SCT without ADHD group had the highest 7R allele frequency, differing significantly from the ADHD without SCT group. Conclusion: The 7R allele of DRD4 gene was found to be significantly more prevalent in SCT cases than in ADHD cases. No substantial neuropsychological differences were found between SCT and ADHD subjects.application/pdfengRevista brasileira de psiquiatria (1999). São Paulo. Vol. 42, n. 6 (2020), p. 630-637.Transtorno do déficit de atenção com hiperatividadeSinais e sintomasCogniçãoPrevalênciaDopaminaGenótipoReceptores de dopamina D4Attention-deficit/hyperactivity disorderSluggish cognitive tempoDopamine transporter geneDopamine receptor D4 genePsychomotor speedDRD4 genotyping may differentiate symptoms of attention-deficit/hyperactivity disorder and sluggish cognitive tempoinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/otherinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001131600.pdf.txt001131600.pdf.txtExtracted Texttext/plain41042http://www.lume.ufrgs.br/bitstream/10183/230710/2/001131600.pdf.txtb0e84be7c89f7a9b70b1fb6257b084f8MD52ORIGINAL001131600.pdfTexto completo (inglês)application/pdf165645http://www.lume.ufrgs.br/bitstream/10183/230710/1/001131600.pdf12a5ced0af5c700bb88d6f67f218e1bcMD5110183/2307102021-11-20 05:56:08.569351oai:www.lume.ufrgs.br:10183/230710Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2021-11-20T07:56:08Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv DRD4 genotyping may differentiate symptoms of attention-deficit/hyperactivity disorder and sluggish cognitive tempo
title DRD4 genotyping may differentiate symptoms of attention-deficit/hyperactivity disorder and sluggish cognitive tempo
spellingShingle DRD4 genotyping may differentiate symptoms of attention-deficit/hyperactivity disorder and sluggish cognitive tempo
Bolat, Hilmi
Transtorno do déficit de atenção com hiperatividade
Sinais e sintomas
Cognição
Prevalência
Dopamina
Genótipo
Receptores de dopamina D4
Attention-deficit/hyperactivity disorder
Sluggish cognitive tempo
Dopamine transporter gene
Dopamine receptor D4 gene
Psychomotor speed
title_short DRD4 genotyping may differentiate symptoms of attention-deficit/hyperactivity disorder and sluggish cognitive tempo
title_full DRD4 genotyping may differentiate symptoms of attention-deficit/hyperactivity disorder and sluggish cognitive tempo
title_fullStr DRD4 genotyping may differentiate symptoms of attention-deficit/hyperactivity disorder and sluggish cognitive tempo
title_full_unstemmed DRD4 genotyping may differentiate symptoms of attention-deficit/hyperactivity disorder and sluggish cognitive tempo
title_sort DRD4 genotyping may differentiate symptoms of attention-deficit/hyperactivity disorder and sluggish cognitive tempo
author Bolat, Hilmi
author_facet Bolat, Hilmi
Ercan, Eyüp Sabri
Bolat, Gül Ünsel
Tahillioğlu, Akın
Yazici, Kemal Utku
Bacanli, Ali
Pariltay, Erhan
Jafari, Duygu Aygüneş
Kosova, Buket
Özgül, Semiha
Rohde, Luis Augusto Paim
Akin, Haluk
author_role author
author2 Ercan, Eyüp Sabri
Bolat, Gül Ünsel
Tahillioğlu, Akın
Yazici, Kemal Utku
Bacanli, Ali
Pariltay, Erhan
Jafari, Duygu Aygüneş
Kosova, Buket
Özgül, Semiha
Rohde, Luis Augusto Paim
Akin, Haluk
author2_role author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Bolat, Hilmi
Ercan, Eyüp Sabri
Bolat, Gül Ünsel
Tahillioğlu, Akın
Yazici, Kemal Utku
Bacanli, Ali
Pariltay, Erhan
Jafari, Duygu Aygüneş
Kosova, Buket
Özgül, Semiha
Rohde, Luis Augusto Paim
Akin, Haluk
dc.subject.por.fl_str_mv Transtorno do déficit de atenção com hiperatividade
Sinais e sintomas
Cognição
Prevalência
Dopamina
Genótipo
Receptores de dopamina D4
topic Transtorno do déficit de atenção com hiperatividade
Sinais e sintomas
Cognição
Prevalência
Dopamina
Genótipo
Receptores de dopamina D4
Attention-deficit/hyperactivity disorder
Sluggish cognitive tempo
Dopamine transporter gene
Dopamine receptor D4 gene
Psychomotor speed
dc.subject.eng.fl_str_mv Attention-deficit/hyperactivity disorder
Sluggish cognitive tempo
Dopamine transporter gene
Dopamine receptor D4 gene
Psychomotor speed
description Objective: Studies to reduce the heterogeneity of attention-deficit/hyperactivity disorder (ADHD) have increased interest in the concept of sluggish cognitive tempo (SCT). The aim of this study was to investigate if the prevalence of two variable-number tandem repeats (VNTRs) located within the 30 -untranslated region of the DAT1 gene and in exon 3 of the dopamine D4 receptor (DRD4) gene differ among four groups (31 subjects with SCT but no ADHD, 146 individuals with ADHD but no SCT, 67 subjects with SCT + ADHD, and 92 healthy controls). Methods: We compared the sociodemographic profiles, neurocognitive domains, and prevalence of two VNTRs in SCT and ADHD subjects versus typically developing (TD) controls. Results: The SCT without ADHD group had a higher proportion of females and lower parental educational attainment. Subjects in this group performed worse on neuropsychological tests, except for psychomotor speed and commission errors, compared to controls. However, the ADHD without SCT group performed significantly worse on all neuropsychological domains than controls. We found that 4R homozygosity for the DRD4 gene was most prevalent in the ADHD without SCT group. The SCT without ADHD group had the highest 7R allele frequency, differing significantly from the ADHD without SCT group. Conclusion: The 7R allele of DRD4 gene was found to be significantly more prevalent in SCT cases than in ADHD cases. No substantial neuropsychological differences were found between SCT and ADHD subjects.
publishDate 2020
dc.date.issued.fl_str_mv 2020
dc.date.accessioned.fl_str_mv 2021-10-14T04:30:44Z
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10183/230710
dc.identifier.issn.pt_BR.fl_str_mv 1516-4446
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dc.relation.ispartof.pt_BR.fl_str_mv Revista brasileira de psiquiatria (1999). São Paulo. Vol. 42, n. 6 (2020), p. 630-637.
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