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Reduced structural connectivity in cortico-striatal-thalamic network in neonates with congenital heart disease.
Ní Bhroin, Megan; Abo Seada, Samy; Bonthrone, Alexandra F; Kelly, Christopher J; Christiaens, Daan; Schuh, Andreas; Pietsch, Maximilian; Hutter, Jana; Tournier, J-Donald; Cordero-Grande, Lucillio; Rueckert, Daniel; Hajnal, Joseph V; Pushparajah, Kuberan; Simpson, John; Edwards, A David; Rutherford, Mary A; Counsell, Serena J; Batalle, Dafnis.
Afiliação
  • Ní Bhroin M; Centre for the Developing Brain, School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK; Trinity College Institute of Neuroscience and Cognitive Systems Group, Discipline of Psychiatry, School of Medicine, Trinity College Dublin, Ireland.
  • Abo Seada S; Centre for the Developing Brain, School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.
  • Bonthrone AF; Centre for the Developing Brain, School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.
  • Kelly CJ; Centre for the Developing Brain, School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.
  • Christiaens D; Centre for the Developing Brain, School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK; Department of Electrical Engineering (ESAT/PSI), KU Leuven, Leuven, Belgium.
  • Schuh A; Department of Computing, Imperial College London, London, UK.
  • Pietsch M; Centre for the Developing Brain, School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.
  • Hutter J; Centre for the Developing Brain, School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.
  • Tournier JD; Centre for the Developing Brain, School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.
  • Cordero-Grande L; Centre for the Developing Brain, School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK; Biomedical Image Technologies, ETSI Telecomunicación, Universidad Politécnica de Madrid & CIBER-BBN, Madrid, Spain.
  • Rueckert D; Department of Computing, Imperial College London, London, UK.
  • Hajnal JV; Centre for the Developing Brain, School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.
  • Pushparajah K; Paediatric Cardiology Department, Evelina London Children's Healthcare, London, UK.
  • Simpson J; Congenital Heart Disease, Evelina London Children's Hospital, London, UK.
  • Edwards AD; Centre for the Developing Brain, School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.
  • Rutherford MA; Centre for the Developing Brain, School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.
  • Counsell SJ; Centre for the Developing Brain, School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK. Electronic address: serena.counsell@kcl.ac.uk.
  • Batalle D; Centre for the Developing Brain, School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK; Department of Forensic and Neurodevelopmental Science, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.
Neuroimage Clin ; 28: 102423, 2020.
Article em En | MEDLINE | ID: mdl-32987301
ABSTRACT
Impaired brain development has been observed in newborns with congenital heart disease (CHD). We performed graph theoretical analyses and network-based statistics (NBS) to assess global brain network topology and identify subnetworks of altered connectivity in infants with CHD prior to cardiac surgery. Fifty-eight infants with critical/serious CHD prior to surgery and 116 matched healthy controls as part of the developing Human Connectome Project (dHCP) underwent MRI on a 3T system and high angular resolution diffusion MRI (HARDI) was obtained. Multi-tissue constrained spherical deconvolution, anatomically constrained probabilistic tractography (ACT) and spherical-deconvolution informed filtering of tractograms (SIFT2) was used to construct weighted structural networks. Network topology was assessed and NBS was used to identify structural connectivity differences between CHD and control groups. Structural networks were partitioned into core and peripheral nodes, and edges classed as core, peripheral, or feeder. NBS identified one subnetwork with reduced structural connectivity in CHD infants involving basal ganglia, amygdala, hippocampus, cerebellum, vermis, and temporal and parieto-occipital lobe, primarily affecting core nodes and edges. However, we did not find significantly different global network characteristics in CHD neonates. This locally affected sub-network with reduced connectivity could explain, at least in part, the neurodevelopmental impairments associated with CHD.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Conectoma / Cardiopatias Congênitas Tipo de estudo: Prognostic_studies Limite: Humans / Infant / Newborn Idioma: En Revista: Neuroimage Clin Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Irlanda

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Conectoma / Cardiopatias Congênitas Tipo de estudo: Prognostic_studies Limite: Humans / Infant / Newborn Idioma: En Revista: Neuroimage Clin Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Irlanda