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Using a semi-automated approach to quantify Unidentified Bright Objects in Neurofibromatosis type 1 and linkages to cognitive and academic outcomes.
Harriott, Emily M; Nguyen, Tin Q; Landman, Bennett A; Barquero, Laura A; Cutting, Laurie E.
Afiliación
  • Harriott EM; Vanderbilt Brain Institute, 465 21(st) Avenue South, Nashville, TN 37212, USA. Electronic address: emily.m.harriott@vanderbilt.edu.
  • Nguyen TQ; Vanderbilt Brain Institute, 465 21(st) Avenue South, Nashville, TN 37212, USA. Electronic address: tin.nguyen@vanderbilt.edu.
  • Landman BA; Department of Electrical Engineering and Computer Science, Vanderbilt University, 2301Vanderbilt Place, Nashville, TN 37235, USA; Vanderbilt Kennedy Center, 110 Magnolia Circle, Nashville, TN 37203, USA. Electronic address: bennett.landman@vanderbilt.edu.
  • Barquero LA; Department of Special Education, Peabody College of Education and Human Development, Vanderbilt University, 110 Magnolia Circle, Nashville, TN 37203, USA. Electronic address: laura.barquero@vanderbilt.edu.
  • Cutting LE; Vanderbilt Brain Institute, 465 21(st) Avenue South, Nashville, TN 37212, USA; Department of Special Education, Peabody College of Education and Human Development, Vanderbilt University, 110 Magnolia Circle, Nashville, TN 37203, USA; Vanderbilt Kennedy Center, 110 Magnolia Circle, Nashville, TN 3720
Magn Reson Imaging ; 98: 17-25, 2023 05.
Article en En | MEDLINE | ID: mdl-36608909
Neurofibromatosis type 1 (NF1) is an autosomal dominant neurocutaneous syndrome that affects multiple organ systems resulting in widespread symptoms, including cognitive deficits. In addition to the criteria required for an NF1 diagnosis, approximately 70% of children with NF1 present with Unidentified Bright Objects (UBOs) or Focal Areas of Signal Intensity, which are hyperintense bright spots seen on T2-weighted magnetic resonance images and seen more prominently on FLAIR magnetic resonance images (Sabol et al., 2011). Current findings relating the presence/absence, quantities, sizes, and locations of these bright spots to cognitive abilities are mixed. To contribute to and hopefully disentangle some of these mixed findings, we explored potential relationships between metrics related to UBOs and cognitive abilities in a sample of 28 children and adolescents with NF1 (M=12.52 years; SD=3.18 years; 16 male). We used the Lesion Segmentation Tool (LST) to automatically detect and segment the UBOs. The LST was able to qualitatively and quantitatively reliably detect UBOs in images of children with NF1. Using these automatically detected and segmented lesions, we found that while controlling for age, biological sex, perceptual IQ, study, and scanner, "total UBO volume", defined as the sum of all the voxels representing all of the UBOs for each participant, helped explain differences in word reading, phonological awareness, and visuospatial skills. These findings contribute to the emerging NF1 literature and help parse the specific deficits that children with NF1 have, to then help improve the efficacy of reading interventions for children with NF1.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neurofibromatosis 1 / Trastornos del Conocimiento / Disfunción Cognitiva Límite: Adolescent / Child / Humans / Male Idioma: En Revista: Magn Reson Imaging Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neurofibromatosis 1 / Trastornos del Conocimiento / Disfunción Cognitiva Límite: Adolescent / Child / Humans / Male Idioma: En Revista: Magn Reson Imaging Año: 2023 Tipo del documento: Article
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