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Predictors of cognitive development in children with neurofibromatosis type 1 and plexiform neurofibromas.
Hou, Yang; Allen, Taryn; Wolters, Pamela L; Toledo-Tamula, Mary Anne; Martin, Staci; Baldwin, Andrea; Reda, Stephanie; Gillespie, Andy; Goodwin, Anne; Widemann, Brigitte C.
Afiliación
  • Hou Y; Department of Family Sciences, University of Kentucky, Lexington, KY, USA.
  • Allen T; NIH Pediatric Oncology Branch, National Cancer Institute, Bethesda, MD, USA.
  • Wolters PL; Clinical Research Directorate, Frederick National Laboratory for Cancer Research sponsored by the National Cancer Institute, Frederick, MD, USA.
  • Toledo-Tamula MA; NIH Pediatric Oncology Branch, National Cancer Institute, Bethesda, MD, USA.
  • Martin S; Clinical Research Directorate, Frederick National Laboratory for Cancer Research sponsored by the National Cancer Institute, Frederick, MD, USA.
  • Baldwin A; NIH Pediatric Oncology Branch, National Cancer Institute, Bethesda, MD, USA.
  • Reda S; Clinical Research Directorate, Frederick National Laboratory for Cancer Research sponsored by the National Cancer Institute, Frederick, MD, USA.
  • Gillespie A; NIH Pediatric Oncology Branch, National Cancer Institute, Bethesda, MD, USA.
  • Goodwin A; NIH Pediatric Oncology Branch, National Cancer Institute, Bethesda, MD, USA.
  • Widemann BC; NIH Pediatric Oncology Branch, National Cancer Institute, Bethesda, MD, USA.
Dev Med Child Neurol ; 62(8): 977-984, 2020 08.
Article en En | MEDLINE | ID: mdl-32052421
AIM: To describe the cognitive development of children with neurofibromatosis type 1 (NF1) and plexiform neurofibromas, and identify predictors of cognitive development. METHOD: Participants included 88 children with NF1 and plexiform neurofibromas (50 males, 38 females, aged 6-18y, mean=12y, SD=3y 7mo) on a natural history study at the National Cancer Institute. Neuropsychological assessments (e.g. IQ, academic achievement, attention, and executive functioning) were administered three times over 6 years. RESULTS: Relative to normative peers, the total sample of children with NF1 and plexiform neurofibromas demonstrated significantly lower scores in most cognitive domains and decreasing z-scores over time in math, writing, inhibitory control, and working memory. Children who had parents with (vs without) NF1 were more likely to experience decreased z-scores in performance IQ, reading, writing, attention, and working memory. Higher (vs lower) parental education was related to higher levels of IQ, math, reading, and cognitive flexibility and a slower decrease in math z-scores. Children's sex and the number of NF1 disease-related complications were not related to most cognitive outcomes. INTERPRETATION: Children with NF1 and plexiform neurofibromas are at high risk for cognitive difficulties and declining z-scores in various domains of cognitive functioning over time. The findings highlight the need for a better understanding of the within-group differences in these children and their need for individualized educational plans. WHAT THIS PAPER ADDS: Math, writing, inhibitory control, and working memory scores decreased over time. The proportion of children with clinically significant cognitive deficits increased over time. Parental neurofibromatosis type 1 and low education were related to greater cognitive difficulties in children.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Desarrollo Infantil / Neurofibromatosis 1 / Cognición / Neurofibroma Plexiforme Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Child / Female / Humans / Male Idioma: En Revista: Dev Med Child Neurol Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Desarrollo Infantil / Neurofibromatosis 1 / Cognición / Neurofibroma Plexiforme Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Child / Female / Humans / Male Idioma: En Revista: Dev Med Child Neurol Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos