A Diffusion Tensor Imaging Study in Children With ADHD, Autism Spectrum Disorder, OCD, and Matched Controls: Distinct and Non-Distinct White Matter Disruption and Dimensional Brain-Behavior Relationships
Objective:Neurodevelopmental disorders (NDDs) (attention deficit hyperactivity disorder [ADHD], autism spectrum disorder [ASD], and obsessive-compulsive disorder [OCD]) share genetic vulnerability and symptom domains. The authors present direct comparison of structural brain circuitry in children an...
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Published in | The American journal of psychiatry Vol. 173; no. 12; pp. 1213 - 1222 |
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Main Authors | , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Psychiatric Association
01.12.2016
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Subjects | |
Online Access | Get full text |
ISSN | 0002-953X 1535-7228 |
DOI | 10.1176/appi.ajp.2016.15111435 |
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Abstract | Objective:Neurodevelopmental disorders (NDDs) (attention deficit hyperactivity disorder [ADHD], autism spectrum disorder [ASD], and obsessive-compulsive disorder [OCD]) share genetic vulnerability and symptom domains. The authors present direct comparison of structural brain circuitry in children and adolescents with NDDs and control subjects and examine brain circuit-behavior relationships across NDDs using dimensional measures related to each disorder.Method:Diffusion imaging and behavioral measures were acquired in 200 children and adolescents (ADHD: N=31; OCD: N=36; ASD: N=71; controls: N=62; mean age range: 10.3–12.6 years). Following Tract-Based Spatial Statistics, multigroup comparison of white matter indices was conducted, followed by pairwise comparisons. Relationships of fractional anisotropy with dimensional measures of inattention, social deficits, obsessive-compulsive symptoms, and general adaptive functioning were conducted across the NDD sample.Results:Lower fractional anisotropy within the splenium of the corpus callosum was found in each NDD group, compared with the control group. Lower fractional anisotropy in additional white matter tracts was found in the ASD and ADHD groups, compared with the control group, but not in the OCD group. Fractional anisotropy was lower in the ASD and ADHD groups compared with the OCD group but was not different in ADHD participants compared with ASD participants. A positive relation between fractional anisotropy (across much of the brain) and general adaptive functioning across NDDs was shown.Conclusions:This study identified disruption in interhemispheric circuitry (i.e., fractional anisotropy alterations in the corpus callosum) as a shared feature of ASD, ADHD, and OCD. However, fractional anisotropy alterations may be more widespread and severe in ASD and ADHD than in OCD. Higher fractional anisotropy throughout the brain appears to be related to better adaptive function across NDDs. |
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AbstractList | Objective:Neurodevelopmental disorders (NDDs) (attention deficit hyperactivity disorder [ADHD], autism spectrum disorder [ASD], and obsessive-compulsive disorder [OCD]) share genetic vulnerability and symptom domains. The authors present direct comparison of structural brain circuitry in children and adolescents with NDDs and control subjects and examine brain circuit-behavior relationships across NDDs using dimensional measures related to each disorder.Method:Diffusion imaging and behavioral measures were acquired in 200 children and adolescents (ADHD: N=31; OCD: N=36; ASD: N=71; controls: N=62; mean age range: 10.3–12.6 years). Following Tract-Based Spatial Statistics, multigroup comparison of white matter indices was conducted, followed by pairwise comparisons. Relationships of fractional anisotropy with dimensional measures of inattention, social deficits, obsessive-compulsive symptoms, and general adaptive functioning were conducted across the NDD sample.Results:Lower fractional anisotropy within the splenium of the corpus callosum was found in each NDD group, compared with the control group. Lower fractional anisotropy in additional white matter tracts was found in the ASD and ADHD groups, compared with the control group, but not in the OCD group. Fractional anisotropy was lower in the ASD and ADHD groups compared with the OCD group but was not different in ADHD participants compared with ASD participants. A positive relation between fractional anisotropy (across much of the brain) and general adaptive functioning across NDDs was shown.Conclusions:This study identified disruption in interhemispheric circuitry (i.e., fractional anisotropy alterations in the corpus callosum) as a shared feature of ASD, ADHD, and OCD. However, fractional anisotropy alterations may be more widespread and severe in ASD and ADHD than in OCD. Higher fractional anisotropy throughout the brain appears to be related to better adaptive function across NDDs. OBJECTIVENeurodevelopmental disorders (NDDs) (attention deficit hyperactivity disorder [ADHD], autism spectrum disorder [ASD], and obsessive-compulsive disorder [OCD]) share genetic vulnerability and symptom domains. The authors present direct comparison of structural brain circuitry in children and adolescents with NDDs and control subjects and examine brain circuit-behavior relationships across NDDs using dimensional measures related to each disorder.METHODDiffusion imaging and behavioral measures were acquired in 200 children and adolescents (ADHD: N=31; OCD: N=36; ASD: N=71; controls: N=62; mean age range: 10.3-12.6 years). Following Tract-Based Spatial Statistics, multigroup comparison of white matter indices was conducted, followed by pairwise comparisons. Relationships of fractional anisotropy with dimensional measures of inattention, social deficits, obsessive-compulsive symptoms, and general adaptive functioning were conducted across the NDD sample.RESULTSLower fractional anisotropy within the splenium of the corpus callosum was found in each NDD group, compared with the control group. Lower fractional anisotropy in additional white matter tracts was found in the ASD and ADHD groups, compared with the control group, but not in the OCD group. Fractional anisotropy was lower in the ASD and ADHD groups compared with the OCD group but was not different in ADHD participants compared with ASD participants. A positive relation between fractional anisotropy (across much of the brain) and general adaptive functioning across NDDs was shown.CONCLUSIONSThis study identified disruption in interhemispheric circuitry (i.e., fractional anisotropy alterations in the corpus callosum) as a shared feature of ASD, ADHD, and OCD. However, fractional anisotropy alterations may be more widespread and severe in ASD and ADHD than in OCD. Higher fractional anisotropy throughout the brain appears to be related to better adaptive function across NDDs. Neurodevelopmental disorders (NDDs) (attention deficit hyperactivity disorder [ADHD], autism spectrum disorder [ASD], and obsessive-compulsive disorder [OCD]) share genetic vulnerability and symptom domains. The authors present direct comparison of structural brain circuitry in children and adolescents with NDDs and control subjects and examine brain circuit-behavior relationships across NDDs using dimensional measures related to each disorder. Diffusion imaging and behavioral measures were acquired in 200 children and adolescents (ADHD: N=31; OCD: N=36; ASD: N=71; controls: N=62; mean age range: 10.3-12.6 years). Following Tract-Based Spatial Statistics, multigroup comparison of white matter indices was conducted, followed by pairwise comparisons. Relationships of fractional anisotropy with dimensional measures of inattention, social deficits, obsessive-compulsive symptoms, and general adaptive functioning were conducted across the NDD sample. Lower fractional anisotropy within the splenium of the corpus callosum was found in each NDD group, compared with the control group. Lower fractional anisotropy in additional white matter tracts was found in the ASD and ADHD groups, compared with the control group, but not in the OCD group. Fractional anisotropy was lower in the ASD and ADHD groups compared with the OCD group but was not different in ADHD participants compared with ASD participants. A positive relation between fractional anisotropy (across much of the brain) and general adaptive functioning across NDDs was shown. This study identified disruption in interhemispheric circuitry (i.e., fractional anisotropy alterations in the corpus callosum) as a shared feature of ASD, ADHD, and OCD. However, fractional anisotropy alterations may be more widespread and severe in ASD and ADHD than in OCD. Higher fractional anisotropy throughout the brain appears to be related to better adaptive function across NDDs. |
Author | Nazeri, Arash Brian, Jessica Arnold, Paul D Lai, Meng-Chuan Soreni, Noam Lerch, Jason P Taylor, Margot J Lee, Wayne Pipitone, Jon Ameis, Stephanie H Szatmari, Peter Anagnostou, Evdokia Voineskos, Aristotle N Croarkin, Paul E Crosbie, Jennifer Schachar, Russell Viviano, Joseph D |
Author_xml | – sequence: 1 givenname: Stephanie H surname: Ameis fullname: Ameis, Stephanie H email: stephanie.ameis@camh.ca – sequence: 2 givenname: Jason P surname: Lerch fullname: Lerch, Jason P email: stephanie.ameis@camh.ca – sequence: 3 givenname: Margot J surname: Taylor fullname: Taylor, Margot J email: stephanie.ameis@camh.ca – sequence: 4 givenname: Wayne surname: Lee fullname: Lee, Wayne email: stephanie.ameis@camh.ca – sequence: 5 givenname: Joseph D surname: Viviano fullname: Viviano, Joseph D email: stephanie.ameis@camh.ca – sequence: 6 givenname: Jon surname: Pipitone fullname: Pipitone, Jon email: stephanie.ameis@camh.ca – sequence: 7 givenname: Arash surname: Nazeri fullname: Nazeri, Arash email: stephanie.ameis@camh.ca – sequence: 8 givenname: Paul E surname: Croarkin fullname: Croarkin, Paul E email: stephanie.ameis@camh.ca – sequence: 9 givenname: Aristotle N surname: Voineskos fullname: Voineskos, Aristotle N email: stephanie.ameis@camh.ca – sequence: 10 givenname: Meng-Chuan surname: Lai fullname: Lai, Meng-Chuan email: stephanie.ameis@camh.ca – sequence: 11 givenname: Jennifer surname: Crosbie fullname: Crosbie, Jennifer email: stephanie.ameis@camh.ca – sequence: 12 givenname: Jessica surname: Brian fullname: Brian, Jessica email: stephanie.ameis@camh.ca – sequence: 13 givenname: Noam surname: Soreni fullname: Soreni, Noam email: stephanie.ameis@camh.ca – sequence: 14 givenname: Russell surname: Schachar fullname: Schachar, Russell email: stephanie.ameis@camh.ca – sequence: 15 givenname: Peter surname: Szatmari fullname: Szatmari, Peter email: stephanie.ameis@camh.ca – sequence: 16 givenname: Paul D surname: Arnold fullname: Arnold, Paul D email: stephanie.ameis@camh.ca – sequence: 17 givenname: Evdokia surname: Anagnostou fullname: Anagnostou, Evdokia email: stephanie.ameis@camh.ca |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/27363509$$D View this record in MEDLINE/PubMed |
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disorders publication-title: Can J Psychiatry – volume: 23 start-page: S208 year: 2004 end-page: S219 article-title: Advances in functional and structural MR image analysis and implementation as FSL publication-title: Neuroimage – volume: 37 start-page: 748 year: 2007 end-page: 759 article-title: Social and communication abilities and disabilities in higher functioning individuals with autism spectrum disorders: the Vineland and the ADOS publication-title: J Autism Dev Disord – volume: 14 start-page: 519 year: 2014 end-page: 538 article-title: Imaging the ADHD brain: disorder-specificity, medication effects and clinical translation publication-title: Expert Rev Neurother – volume: 40 start-page: 580 year: 2010 end-page: 589 article-title: Autism and ADHD symptoms in patients with OCD: are they associated with specific OC symptom dimensions or OC symptom severity? publication-title: J Autism Dev Disord – volume: 54 start-page: 26 year: 2014 end-page: 35 article-title: Diffusion tensor 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Snippet | Objective:Neurodevelopmental disorders (NDDs) (attention deficit hyperactivity disorder [ADHD], autism spectrum disorder [ASD], and obsessive-compulsive... Neurodevelopmental disorders (NDDs) (attention deficit hyperactivity disorder [ADHD], autism spectrum disorder [ASD], and obsessive-compulsive disorder [OCD])... Objective: Neurodevelopmental disorders (NDDs) (attention deficit hyperactivity disorder [ADHD], autism spectrum disorder [ASD], and obsessive-compulsive... OBJECTIVENeurodevelopmental disorders (NDDs) (attention deficit hyperactivity disorder [ADHD], autism spectrum disorder [ASD], and obsessive-compulsive... |
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SubjectTerms | Adaptation, Psychological Anisotropy Attention Attention Deficit Disorder with Hyperactivity - pathology Attention Deficit Disorder with Hyperactivity - psychology Attention deficit hyperactivity disorder Autism Autism Spectrum Disorder - pathology Autism Spectrum Disorder - psychology Brain Brain - pathology Case-Control Studies Child Children & youth Comparative analysis Diffusion Tensor Imaging Female Humans Male Neuroimaging Obsessive-Compulsive Disorder - pathology Obsessive-Compulsive Disorder - psychology Social Behavior White Matter - pathology |
Title | A Diffusion Tensor Imaging Study in Children With ADHD, Autism Spectrum Disorder, OCD, and Matched Controls: Distinct and Non-Distinct White Matter Disruption and Dimensional Brain-Behavior Relationships |
URI | http://dx.doi.org/10.1176/appi.ajp.2016.15111435 https://www.ncbi.nlm.nih.gov/pubmed/27363509 https://www.proquest.com/docview/1846272772 https://www.proquest.com/docview/1826714066 |
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