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PMID: 32642741 Published · epublish English

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

Neuro-oncology advances ·Vol. 2 ·No. Suppl 1 ·2020-07-00

de Blank P, Berman JI, Prelack M, Sollee JR, Lane A, Waldman AT, Fisher MJ

Abstract

Adults with neurofibromatosis type 1 (NF1) have decreased white matter integrity, but differences in children with NF1 have not been described. Defining normal values for diffusion tensor imaging (DTI) measures, especially in the optic radiations, is important to the development of DTI as a potential biomarker of visual acuity in children with optic pathway glioma. This study examines the effect of age and NF1 status on DTI measures in children. In this retrospective study, MR imaging including DTI was conducted in 93 children (40 children with NF1 and 53 healthy controls) between 0 and 14 years of age. Regression models of age, sex, and NF1 status on DTI measures were evaluated, and tract-based spatial statistics (TBSS) compared DTI measures in age-matched NF1 to non-NF1 cohorts. Fractional anisotropy, radial diffusivity, and mean diffusivity in white matter tracts of the optic radiations varied with age and were best modeled by a logarithmic function. Age-related DTI measure change was different in NF1 versus non-NF1 subjects. Normal values and 95% confidence intervals for age 0.5-12 years were derived for both groups. Differences in DTI measures between NF1 and non-NF1 groups at a range of ages were shown diffusely throughout the cerebral white matter using TBSS. Children with NF1 demonstrate increased diffusion throughout the brain compared to children without NF1 suggesting a potentially altered developmental trajectory of optic radiation microstructure. Defining normal values for white matter integrity in children with NF1 may help target early intervention efforts in this vulnerable group.

Keywords
diffusion tensor imaging neurofibromatosis type 1 optic pathway glioma vision white matter development
Article Info
Journal
Neuro-oncology advances
Abbr.
Neurooncol Adv
ISSN
2632-2498
Published
2020-07-00
Language
English
Country/Region
England
NLM ID
101755003
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