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Brain Circuit Alterations and Cognitive Disability in Late-Onset Cobalamin D Disorder.
De Las Heras, Javier; Diez, Ibai; Jimenez-Marin, Antonio; Cabrera, Alberto; Ramos-Usuga, Daniela; Diaz-Fernandez, Marta Venecia; Torices, Leire; Nunes-Xavier, Caroline E; Pulido, Rafael; Arango-Lasprilla, Juan Carlos; Cortes, Jesus M.
Afiliação
  • De Las Heras J; Division of Pediatric Metabolism, Cruces University Hospital, 48903 Barakaldo, Spain.
  • Diez I; Inborn Errors of Metabolism Group, Biocruces Bizkaia Health Research Institute, 48903 Barakaldo, Spain.
  • Jimenez-Marin A; Department of Pediatrics, University of the Basque Country (UPV/EHU), 48940 Leioa, Spain.
  • Cabrera A; Gordon Center for Medical Imaging, Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02115, USA.
  • Ramos-Usuga D; Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02129, USA.
  • Diaz-Fernandez MV; Neurotechnology Laboratory, Tecnalia Health Department, 48160 Derio, Spain.
  • Torices L; Computational Neuroimaging Group, Biocruces Bizkaia Health Research Institute, 48903 Barakaldo, Spain.
  • Nunes-Xavier CE; Biomedical Research Doctorate Program, University of the Basque Country (UPV/EHU), 48940 Leioa, Spain.
  • Pulido R; Osatek, 48011 Vitoria-Gazteiz, Spain.
  • Arango-Lasprilla JC; Biomedical Research Doctorate Program, University of the Basque Country (UPV/EHU), 48940 Leioa, Spain.
  • Cortes JM; Biocruces Bizkaia Health Research Institute, 48903 Barakaldo, Spain.
J Clin Med ; 9(4)2020 Apr 02.
Article em En | MEDLINE | ID: mdl-32252256
ABSTRACT
Neuroimaging studies describing brain circuits' alterations in cobalamin (vitamin B12)-deficient patients are limited and have not been carried out in patients with inborn errors of cobalamin metabolism. The objective of this study was to assess brain functionality and brain circuit alterations in a patient with an ultra-rare inborn error of cobalamin metabolism, methylmalonic aciduria, and homocystinuria due to cobalamin D disease, as compared with his twin sister as a healthy control (HC). We acquired magnetic resonance imaging (including structural, functional, and diffusion images) to calculate brain circuit abnormalities and combined these results with the scores after a comprehensive neuropsychological evaluation. As compared with HC, the patient had severe patterns of damage, such as a 254% increment of ventricular volume, pronounced subcortical and cortical atrophies (mainly at striatum, cingulate cortex, and precuneus), and connectivity alterations at fronto-striato-thalamic circuit, cerebellum, and corpus callosum. In agreement with brain circuit alterations, cognitive deficits existed in attention, executive function, inhibitory control, and mental flexibility. This is the first study that provides the clinical, genetic, neuroanatomical, neuropsychological, and psychosocial characterization of a patient with the cobalamin D disorder, showing functional alterations in central nervous system motor tracts, thalamus, cerebellum, and basal ganglia, that, as far as we know, have not been reported yet in vitamin B12-related disorders.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Clin Med Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Espanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Clin Med Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Espanha