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Constructing an Axonal‐Specific Myelin Developmental Graph and its Application to Childhood Absence Epilepsy

BACKGROUND AND PURPOSE: The process of myelination starts in utero around 20 weeks of gestation and continues through adulthood. We first set out to characterize the maturation of the tract‐specific myelin content in healthy subjects from childhood (7‐12 years) into adulthood (18‐32 years). Second,...

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Detalles Bibliográficos
Autores principales: Drenthen, Gerhard S., Fonseca Wald, Eric L. A., Backes, Walter H., Aldenkamp, Albert P., Vermeulen, R. Jeroen, Debeij‐van Hall, Mariette H. J. A., Klinkenberg, Sylvia, Jansen, Jacobus F. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7317939/
https://www.ncbi.nlm.nih.gov/pubmed/32255537
http://dx.doi.org/10.1111/jon.12707
Descripción
Sumario:BACKGROUND AND PURPOSE: The process of myelination starts in utero around 20 weeks of gestation and continues through adulthood. We first set out to characterize the maturation of the tract‐specific myelin content in healthy subjects from childhood (7‐12 years) into adulthood (18‐32 years). Second, we apply the resulting development graph to children with childhood absence epilepsy (CAE), a pediatric epilepsy that was previously characterized by changes in myelin content. METHODS: In a prospective cross‐sectional study, 15 healthy children (7‐12 years), 14 healthy adult participants (18‐32 years) and 17 children with a clinical diagnosis of CAE (6‐12 years) were included. For each participant, diffusion weighted images were acquired to reconstruct bundles of white matter tracts and multi‐echo multi‐slice GRASE images were acquired for myelin‐water estimation. Subsequently, a tract‐specific myelin development graph was constructed using the percentual difference in myelin‐water content from childhood (12 year) to adulthood (25 year). RESULTS: The graph revealed myelination patterns, where tracts in the central regions myelinate prior to peripheral tracts and intra‐hemispheric tracts as well as tracts in the left hemisphere myelinate prior to inter‐hemispheric tracts and tracts in the right hemisphere, respectively. No significant differences were found in myelin‐water content between children with CAE and healthy children for neither the early developing tracts, nor the tracts that develop in a later stage. However, the difference between the myelin‐water of late and early developing tracts is significantly smaller in the children with CAE. CONCLUSION: These results indicate that CAE is associated with widespread neurodevelopmental myelin differences.