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Neurite density of white matter significantly correlates with tuberous sclerosis complex disease severity

OBJECTIVE: To assess whether white matter (WM) diffusion tensor imaging (DTI) and neurite orientation dispersion and density imaging (NODDI) derived measures correlate with tuberous sclerosis complex (TSC) disease severity. COHORT AND METHODS: A multi-shell diffusion protocol was added to the clinic...

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Autores principales: Anaby, Debbie, Shrot, Shai, Belenky, Eugenia, Ben-Zeev, Bruria, Tzadok, Michal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9421460/
https://www.ncbi.nlm.nih.gov/pubmed/35780663
http://dx.doi.org/10.1016/j.nicl.2022.103085
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author Anaby, Debbie
Shrot, Shai
Belenky, Eugenia
Ben-Zeev, Bruria
Tzadok, Michal
author_facet Anaby, Debbie
Shrot, Shai
Belenky, Eugenia
Ben-Zeev, Bruria
Tzadok, Michal
author_sort Anaby, Debbie
collection PubMed
description OBJECTIVE: To assess whether white matter (WM) diffusion tensor imaging (DTI) and neurite orientation dispersion and density imaging (NODDI) derived measures correlate with tuberous sclerosis complex (TSC) disease severity. COHORT AND METHODS: A multi-shell diffusion protocol was added to the clinical MRI brain scans of thirteen patients including 6 males and 7 females with a mean ± std age of 17.2 ± 5.8 years. Fractional anisotropy (FA) and mean diffusivity (MD) were generated from DTI and neurite density index (NDI), orientation dispersion index (ODI) and free water index (fiso) were generated from NODDI. A clinical score was determined for each patient according to the existence of epilepsy, developmental delay, autism or psychiatric disorders. Whole-brain segmented WM was averaged for each parametric map and 3 group k-means clustering was performed on the NDI and FA maps. MRI quantitative parameters were correlated with the clinical scores. RESULTS: Segmented whole brain WM averages of MD and NDI values showed significant negative (p = 0.0058) and positive (p = 0.0092) correlations with the clinical scores, respectively. Additionally, the contribution of the low and high NDI-based clusters to the whole brain WM significantly correlated with the clinical scores (p = 0.03 and p = 0.00047, respectively). No correlation was found when the clusters were based on the FA maps. CONCLUSION: Advanced diffusion MRI of TSC patients revealed widespread WM alterations. Neurite density showed significant correlations with disease severity and is therefore suggested to reflect an underlying biological process in TSC WM. The quantification of WM alterations by advanced diffusion MRI may be an additional biomarker for TSC and may be advantageous as a complementary MR protocol for the evaluation of TSC patients.
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spelling pubmed-94214602022-08-30 Neurite density of white matter significantly correlates with tuberous sclerosis complex disease severity Anaby, Debbie Shrot, Shai Belenky, Eugenia Ben-Zeev, Bruria Tzadok, Michal Neuroimage Clin Regular Article OBJECTIVE: To assess whether white matter (WM) diffusion tensor imaging (DTI) and neurite orientation dispersion and density imaging (NODDI) derived measures correlate with tuberous sclerosis complex (TSC) disease severity. COHORT AND METHODS: A multi-shell diffusion protocol was added to the clinical MRI brain scans of thirteen patients including 6 males and 7 females with a mean ± std age of 17.2 ± 5.8 years. Fractional anisotropy (FA) and mean diffusivity (MD) were generated from DTI and neurite density index (NDI), orientation dispersion index (ODI) and free water index (fiso) were generated from NODDI. A clinical score was determined for each patient according to the existence of epilepsy, developmental delay, autism or psychiatric disorders. Whole-brain segmented WM was averaged for each parametric map and 3 group k-means clustering was performed on the NDI and FA maps. MRI quantitative parameters were correlated with the clinical scores. RESULTS: Segmented whole brain WM averages of MD and NDI values showed significant negative (p = 0.0058) and positive (p = 0.0092) correlations with the clinical scores, respectively. Additionally, the contribution of the low and high NDI-based clusters to the whole brain WM significantly correlated with the clinical scores (p = 0.03 and p = 0.00047, respectively). No correlation was found when the clusters were based on the FA maps. CONCLUSION: Advanced diffusion MRI of TSC patients revealed widespread WM alterations. Neurite density showed significant correlations with disease severity and is therefore suggested to reflect an underlying biological process in TSC WM. The quantification of WM alterations by advanced diffusion MRI may be an additional biomarker for TSC and may be advantageous as a complementary MR protocol for the evaluation of TSC patients. Elsevier 2022-06-22 /pmc/articles/PMC9421460/ /pubmed/35780663 http://dx.doi.org/10.1016/j.nicl.2022.103085 Text en © 2022 Published by Elsevier Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
Anaby, Debbie
Shrot, Shai
Belenky, Eugenia
Ben-Zeev, Bruria
Tzadok, Michal
Neurite density of white matter significantly correlates with tuberous sclerosis complex disease severity
title Neurite density of white matter significantly correlates with tuberous sclerosis complex disease severity
title_full Neurite density of white matter significantly correlates with tuberous sclerosis complex disease severity
title_fullStr Neurite density of white matter significantly correlates with tuberous sclerosis complex disease severity
title_full_unstemmed Neurite density of white matter significantly correlates with tuberous sclerosis complex disease severity
title_short Neurite density of white matter significantly correlates with tuberous sclerosis complex disease severity
title_sort neurite density of white matter significantly correlates with tuberous sclerosis complex disease severity
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9421460/
https://www.ncbi.nlm.nih.gov/pubmed/35780663
http://dx.doi.org/10.1016/j.nicl.2022.103085
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