Decreasing ADHD phenotypic heterogeneity: searching for neurobiological underpinnings of the restrictive inattentive phenotype

dc.contributor.authorErcan, Eyup Sabri
dc.contributor.authorSuren, Serkan
dc.contributor.authorBacanli, Ali
dc.contributor.authorYazici, Kemal Utku
dc.contributor.authorCalli, Cem
dc.contributor.authorOzyurt, Onur
dc.contributor.authorRohde, Luis Augusto
dc.date.accessioned2026-08-12T17:48:43Z
dc.date.issued2016
dc.departmentFırat Üniversitesi
dc.description.abstractDuring the process of developing the DSM-5, a new phenotype of ADHD was proposed-the ADHD restrictive inattentive presentation (ADHD-RI), describing subjects with high endorsement of inattentive symptoms and a low level of hyperactivity. However, this phenotype was not included in the DSM-5 because of the lack of robust neurobiological data. We aimed to assess the specific neurobiological underpinnings of individuals presenting ADHD-RI. We compared a sample of 301 subjects (101 ADHD-Combined; 50 ADHD-RI; 50 ADHD predominantly inattentive type and 100 typically developing subjects) aged 8-15 years, using a complete neuropsychological battery, molecular genetic data (DRD4 and DAT1 most studied polymorphisms) and functional MRI during a Go-No/Go task. Subjects with ADHD-RI had a significantly different neuropsychological profile compared with the other groups, including lower psychomotor speeds, longer reaction times and the worst overall performance in the global neurocognitive index. The proportion of subjects with the presence of DRD4-7 repeat allele was significantly higher in ADHD-RI. The fMRI data suggested that more attention-related posterior brain regions (especially temporo-occipital areas) are activated in ADHD-RI during both Go and No-Go cues compared to TD controls and ADHD predominantly inattentive type. ADHD-RI may represent a different phenotype than other types of ADHD. In addition, our results suggest that reducing the phenotypic heterogeneity may aid in the search for the neurobiological underpinnings of ADHD.
dc.description.sponsorshipEge University Scientific Research Project Commission, Izmir, Turkey; National Council for Scientific and Technological Development (CNPq, Brazil); Hospital de Clinicas de Porto Alegre (HCPA), Porto Alegre, Brazil
dc.description.sponsorshipThis work was partially supported by research grants from the following: Ege University Scientific Research Project Commission, Izmir, Turkey, the National Council for Scientific and Technological Development (CNPq, Brazil), and Hospital de Clinicas de Porto Alegre (HCPA), Porto Alegre, Brazil. The authors thank Dr Cahide Aydin for contribution in case enrollment process.
dc.identifier.doi10.1007/s00787-015-0731-3
dc.identifier.endpage282
dc.identifier.issn1018-8827
dc.identifier.issn1435-165X
dc.identifier.issue3
dc.identifier.orcid0000-0003-3636-6082
dc.identifier.orcid0000-0001-9479-6190
dc.identifier.orcid0000-0003-3200-5140
dc.identifier.orcid0000-0002-4552-4188
dc.identifier.orcid0000-0002-1552-1090
dc.identifier.orcid0000-0003-4756-7365
dc.identifier.orcid0000-0002-6577-0335
dc.identifier.pmid26058607
dc.identifier.scopus2-s2.0-84959143252
dc.identifier.scopusqualityQ1
dc.identifier.startpage273
dc.identifier.urihttps://doi.org/10.1007/s00787-015-0731-3
dc.identifier.urihttps://hdl.handle.net/11508/61535
dc.identifier.volume25
dc.identifier.wosWOS:000371261200006
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherSpringer
dc.relation.ispartofEuropean Child & Adolescent Psychiatry
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.subjectADHD
dc.subjectPhenotype
dc.subjectNeuropsychology
dc.subjectNeuroimaging
dc.subjectMolecular genetics
dc.subjectHyperactivity
dc.titleDecreasing ADHD phenotypic heterogeneity: searching for neurobiological underpinnings of the restrictive inattentive phenotype
dc.typeArticle

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