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Integrity of the corpus callosum in patients with periventricular nodular heterotopia related epilepsy by FLNA mutation
OBJECTIVE: To investigate the quantitative diffusion properties of the corpus callosum (CC) in a large group of patients with periventricular nodular heterotopia (PNH) related epilepsy and to further investigate the effect of Filamin A (FLNA) mutation on these properties. METHODS: Patients with PNH...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5647519/ https://www.ncbi.nlm.nih.gov/pubmed/29062687 http://dx.doi.org/10.1016/j.nicl.2017.10.002 |
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author | Liu, Wenyu An, Dongmei Niu, Running Gong, Qiyong Zhou, Dong |
author_facet | Liu, Wenyu An, Dongmei Niu, Running Gong, Qiyong Zhou, Dong |
author_sort | Liu, Wenyu |
collection | PubMed |
description | OBJECTIVE: To investigate the quantitative diffusion properties of the corpus callosum (CC) in a large group of patients with periventricular nodular heterotopia (PNH) related epilepsy and to further investigate the effect of Filamin A (FLNA) mutation on these properties. METHODS: Patients with PNH (n = 34), subdivided into FLNA-mutated (n = 11) and FLNA-nonmutated patients (n = 23) and healthy controls (n = 34), underwent 3.0 T structural MRI and diffusion imaging scan (64 direction). Fractional anisotropy (FA) and mean diffusivity (MD) were measured in the three major subdivisions of the CC (genu, body and splenium). Correlations between DTI metric changes and clinical parameters were also evaluated. Furthermore, the effect of FLNA mutation on structural integrity of the corpus callosum was examined. RESULTS: Patients with PNH and epilepsy had significant reductions in FA for the genu and splenium of the CC, accompanied by increases in MD for the splenium, as compared to healthy controls. There were no correlations between clinical parameters of epilepsy and MD. The FA value in the splenium negatively correlated with epilepsy duration. Interestingly, FLNA-mutated patients showed significantly decreased FA for all three major subdivisions of the CC, and increased MD for the genu and splenium, as compared to HCs and FLNA-nonmutated patients. CONCLUSIONS: These findings support the conclusion that patients with epilepsy secondary to PNH present widespread microstructural changes found in the corpus callosum that extend beyond the macroscopic MRI-visible lesions. This study also indicates that FLNA may affect white matter integrity in this disorder. |
format | Online Article Text |
id | pubmed-5647519 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-56475192017-10-23 Integrity of the corpus callosum in patients with periventricular nodular heterotopia related epilepsy by FLNA mutation Liu, Wenyu An, Dongmei Niu, Running Gong, Qiyong Zhou, Dong Neuroimage Clin Regular Article OBJECTIVE: To investigate the quantitative diffusion properties of the corpus callosum (CC) in a large group of patients with periventricular nodular heterotopia (PNH) related epilepsy and to further investigate the effect of Filamin A (FLNA) mutation on these properties. METHODS: Patients with PNH (n = 34), subdivided into FLNA-mutated (n = 11) and FLNA-nonmutated patients (n = 23) and healthy controls (n = 34), underwent 3.0 T structural MRI and diffusion imaging scan (64 direction). Fractional anisotropy (FA) and mean diffusivity (MD) were measured in the three major subdivisions of the CC (genu, body and splenium). Correlations between DTI metric changes and clinical parameters were also evaluated. Furthermore, the effect of FLNA mutation on structural integrity of the corpus callosum was examined. RESULTS: Patients with PNH and epilepsy had significant reductions in FA for the genu and splenium of the CC, accompanied by increases in MD for the splenium, as compared to healthy controls. There were no correlations between clinical parameters of epilepsy and MD. The FA value in the splenium negatively correlated with epilepsy duration. Interestingly, FLNA-mutated patients showed significantly decreased FA for all three major subdivisions of the CC, and increased MD for the genu and splenium, as compared to HCs and FLNA-nonmutated patients. CONCLUSIONS: These findings support the conclusion that patients with epilepsy secondary to PNH present widespread microstructural changes found in the corpus callosum that extend beyond the macroscopic MRI-visible lesions. This study also indicates that FLNA may affect white matter integrity in this disorder. Elsevier 2017-10-13 /pmc/articles/PMC5647519/ /pubmed/29062687 http://dx.doi.org/10.1016/j.nicl.2017.10.002 Text en © 2017 Published by Elsevier Inc. http://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 Liu, Wenyu An, Dongmei Niu, Running Gong, Qiyong Zhou, Dong Integrity of the corpus callosum in patients with periventricular nodular heterotopia related epilepsy by FLNA mutation |
title | Integrity of the corpus callosum in patients with periventricular nodular heterotopia related epilepsy by FLNA mutation |
title_full | Integrity of the corpus callosum in patients with periventricular nodular heterotopia related epilepsy by FLNA mutation |
title_fullStr | Integrity of the corpus callosum in patients with periventricular nodular heterotopia related epilepsy by FLNA mutation |
title_full_unstemmed | Integrity of the corpus callosum in patients with periventricular nodular heterotopia related epilepsy by FLNA mutation |
title_short | Integrity of the corpus callosum in patients with periventricular nodular heterotopia related epilepsy by FLNA mutation |
title_sort | integrity of the corpus callosum in patients with periventricular nodular heterotopia related epilepsy by flna mutation |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5647519/ https://www.ncbi.nlm.nih.gov/pubmed/29062687 http://dx.doi.org/10.1016/j.nicl.2017.10.002 |
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