Literature DB >> 27423006

Relationship between the corpus callosum and neurocognitive disabilities in children with NF-1: diffusion tensor imaging features.

Sinem Aydin1, Serpil Kurtcan2, Alpay Alkan2, Serhat Guler3, Mekiya Filiz4, Temel Fatih Yilmaz2, Turkan Uygur Sahin3, Ayse Aralasmak2.   

Abstract

PURPOSE: Mild neurocognitive disabilities are commonly observed in children with neurofibromatosis type 1 (NF-1). Enlargement of the corpus callosum (CC) is one of the findings in NF-1, but the pathogenesis has not yet been clarified. In this study, we investigated whether diffusion tensor imaging (DTI) features of CC differed between children with NF-1 and healthy control subjects, and we tried to evaluate the association between the microstructural integrity of CC and neurocognitive disabilities, based on apparent diffusion coefficient (ADC) and fractional anisotropy (FA) values.
MATERIALS AND METHODS: The study population consisted of 37 children with NF-1 and 31 healthy controls. Midsagittal CC surface area measurements were obtained from volumetric sagittal T1-weighted turbo spin echo images. FA and ADC values were obtained from the genu and splenium of CC. The results were compared to that of controls. The correlations between neurocognitive test results and measurements of ADC, FA, and surface areas of midsagittal CC in NF-1 patients were investigated.
RESULTS: Total CC area in children with NF-1 was significantly larger than healthy controls. ADC values obtained from the genu of CC were significantly higher in NF-1 children. A negative correlation was observed between the ADC values of the genu of the CC and the arithmetic and digit span scores and between the FA values of the genu and coding scores in children with NF-1.
CONCLUSION: The DTI changes in the genu of CC in children with NF-1 may indicate subtle structural damage, although conventional MRI is normal. ADC and FA changes in the genu may be due to loss of axonal integrity and vasogenic-like edema in the axons responsible for some intellectual functions. DTI may help clarify the underlying pathophysiology of CC changes in relation to neurocognitive function disorders in children with NF1.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Corpus callosum; Demyelination; Diffusion tensor imaging; Neurofibromatosis type 1

Mesh:

Year:  2016        PMID: 27423006     DOI: 10.1016/j.clinimag.2016.06.013

Source DB:  PubMed          Journal:  Clin Imaging        ISSN: 0899-7071            Impact factor:   1.605


  6 in total

1.  Discriminating between neurofibromatosis-1 and typically developing children by means of multimodal MRI and multivariate analyses.

Authors:  Federico Nemmi; Fabien Cignetti; Christine Assaiante; Stephanie Maziero; Fredrique Audic; Patrice Péran; Yves Chaix
Journal:  Hum Brain Mapp       Date:  2019-05-11       Impact factor: 5.038

2.  Neuroanatomical correlates of working memory performance in Neurofibromatosis 1.

Authors:  Cameron Sawyer; Jonathan Green; Ben Lim; Gorana Pobric; JeYoung Jung; Grace Vassallo; D Gareth Evans; Charlotte J Stagg; Laura M Parkes; Stavros Stivaros; Nils Muhlert; Shruti Garg
Journal:  Cereb Cortex Commun       Date:  2022-05-19

Review 3.  Cognitive and Behavioral Disorders in Children with Neurofibromatosis Type 1.

Authors:  Martha Milade Torres Nupan; Alberto Velez Van Meerbeke; Claudia Alejandra López Cabra; Paula Marcela Herrera Gomez
Journal:  Front Pediatr       Date:  2017-10-30       Impact factor: 3.418

4.  Effect of age and neurofibromatosis type 1 status on white matter integrity in the optic radiations.

Authors:  Peter de Blank; Jeffrey I Berman; Marisa Prelack; John R Sollee; Adam Lane; Amy T Waldman; Michael J Fisher
Journal:  Neurooncol Adv       Date:  2020-06-25

5.  Assessment of Auditory Pathways Using Diffusion Tensor Imaging in Patients with Neurofibromatosis Type 1.

Authors:  Sedat Meydan; Sinem Aydin; Hafize Otcu; Serkan Kitis; Alpay Alkan
Journal:  Curr Med Imaging Rev       Date:  2019

6.  White matter is increased in the brains of adults with neurofibromatosis 1.

Authors:  Ralph Buchert; Victor-Felix Mautner; Su Wang; Jan M Friedman; Per Suppa
Journal:  Orphanet J Rare Dis       Date:  2022-03-05       Impact factor: 4.123

  6 in total

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