TY - JOUR
T1 - Child Developmental MRI (CDM) project
T2 - protocol for a multi-centre, cross-sectional study on elucidating the pathophysiology of attention-deficit/hyperactivity disorder and autism spectrum disorder through a multi-dimensional approach
AU - Yamashita, Masatoshi
AU - Kagitani-Shimono, Kuriko
AU - Hirano, Yoshiyuki
AU - Hamatani, Sayo
AU - Nishitani, Shota
AU - Yao, Akiko
AU - Kurata, Sawa
AU - Kosaka, Hirotaka
AU - Jung, Minyoung
AU - Yoshida, Tokiko
AU - Sasaki, Tsuyoshi
AU - Matsumoto, Koji
AU - Kato, Yoko
AU - Nakanishi, Mariko
AU - Tachibana, Masaya
AU - Mohri, Ikuko
AU - Tsuchiya, Kenji J.
AU - Tsujikawa, Tetsuya
AU - Okazawa, Hidehiko
AU - Shimizu, Eiji
AU - Taniike, Masako
AU - Tomoda, Akemi
AU - Mizuno, Yoshifumi
N1 - Publisher Copyright:
© Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
PY - 2023/6/23
Y1 - 2023/6/23
N2 - Introduction Neuroimaging studies on attention-deficit/hyperactivity disorder (ADHD) and autism spectrum disorder (ASD) have demonstrated differences in extensive brain structure, activity and network. However, there remains heterogeneity and inconsistency across these findings, presumably because of the diversity of the disorders themselves, small sample sizes, and site and parameter differences in MRI scanners, and their overall pathogenesis remains unclear. To address these gaps in the literature, we will apply the travelling-subject approach to correct site differences in MRI scanners and clarify brain structure and network characteristics of children with ADHD and ASD using large samples collected in a multi-centre collaboration. In addition, we will investigate the relationship between these characteristics and genetic, epigenetic, biochemical markers, and behavioural and psychological measures. Methods and analysis We will collect resting-state functional MRI (fMRI) and T1-weighted and diffusion-weighted MRI data from 15 healthy adults as travelling subjects and 300 children (ADHD, n=100; ASD, n=100; and typical development, n=100) with multi-dimensional assessments. We will also apply data from more than 1000 samples acquired in our previous neuroimaging studies on ADHD and ASD. Ethics and dissemination The study protocol has been approved by the Research Ethics Committee of the University of Fukui Hospital (approval no: 20220601). Our study findings will be submitted to scientific peer-reviewed journals and conferences.
AB - Introduction Neuroimaging studies on attention-deficit/hyperactivity disorder (ADHD) and autism spectrum disorder (ASD) have demonstrated differences in extensive brain structure, activity and network. However, there remains heterogeneity and inconsistency across these findings, presumably because of the diversity of the disorders themselves, small sample sizes, and site and parameter differences in MRI scanners, and their overall pathogenesis remains unclear. To address these gaps in the literature, we will apply the travelling-subject approach to correct site differences in MRI scanners and clarify brain structure and network characteristics of children with ADHD and ASD using large samples collected in a multi-centre collaboration. In addition, we will investigate the relationship between these characteristics and genetic, epigenetic, biochemical markers, and behavioural and psychological measures. Methods and analysis We will collect resting-state functional MRI (fMRI) and T1-weighted and diffusion-weighted MRI data from 15 healthy adults as travelling subjects and 300 children (ADHD, n=100; ASD, n=100; and typical development, n=100) with multi-dimensional assessments. We will also apply data from more than 1000 samples acquired in our previous neuroimaging studies on ADHD and ASD. Ethics and dissemination The study protocol has been approved by the Research Ethics Committee of the University of Fukui Hospital (approval no: 20220601). Our study findings will be submitted to scientific peer-reviewed journals and conferences.
KW - Child & adolescent psychiatry
KW - Developmental neurology & neurodisability
KW - Paediatric neurology
UR - http://www.scopus.com/inward/record.url?scp=85162747502&partnerID=8YFLogxK
U2 - 10.1136/bmjopen-2022-070157
DO - 10.1136/bmjopen-2022-070157
M3 - Article
C2 - 37355265
AN - SCOPUS:85162747502
SN - 2044-6055
VL - 13
JO - BMJ Open
JF - BMJ Open
IS - 6
M1 - e070157
ER -