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Maturation of cortical microstructure and cognitive development in childhood and adolescence: A T1w/T2w ratio MRI study

The restructuring and optimization of the cerebral cortex from early childhood and through adolescence is an essential feature of human brain development, underlying immense cognitive improvements. Beyond established morphometric cortical assessments, the T1w/T2w ratio quantifies partly separate bio...

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Autores principales: Norbom, Linn B., Rokicki, Jaroslav, Alnæs, Dag, Kaufmann, Tobias, Doan, Nhat Trung, Andreassen, Ole A., Westlye, Lars T., Tamnes, Christian K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7555087/
https://www.ncbi.nlm.nih.gov/pubmed/32744409
http://dx.doi.org/10.1002/hbm.25149
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author Norbom, Linn B.
Rokicki, Jaroslav
Alnæs, Dag
Kaufmann, Tobias
Doan, Nhat Trung
Andreassen, Ole A.
Westlye, Lars T.
Tamnes, Christian K.
author_facet Norbom, Linn B.
Rokicki, Jaroslav
Alnæs, Dag
Kaufmann, Tobias
Doan, Nhat Trung
Andreassen, Ole A.
Westlye, Lars T.
Tamnes, Christian K.
author_sort Norbom, Linn B.
collection PubMed
description The restructuring and optimization of the cerebral cortex from early childhood and through adolescence is an essential feature of human brain development, underlying immense cognitive improvements. Beyond established morphometric cortical assessments, the T1w/T2w ratio quantifies partly separate biological processes, and might inform models of typical neurocognitive development and developmental psychopathology. In the present study, we computed vertex‐wise T1w/T2w ratio across the cortical surface in 621 youths (3–21 years) sampled from the Pediatric Imaging, Neurocognition, and Genetics (PING) study and tested for associations with individual differences in age, sex, and both general and specific cognitive abilities. The results showed a near global linear age‐related increase in T1w/T2w ratio across the brain surface, with a general posterior to anterior increasing gradient in association strength. Moreover, results indicated that boys in late adolescence had regionally higher T1w/T2w ratio as compared to girls. Across individuals, T1w/T2w ratio was negatively associated with general and several specific cognitive abilities mainly within anterior cortical regions. Our study indicates age‐related differences in T1w/T2w ratio throughout childhood, adolescence, and young adulthood, in line with the known protracted myelination of the cortex. Moreover, the study supports T1w/T2w ratio as a promising surrogate measure of individual differences in intracortical brain structure in neurodevelopment.
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spelling pubmed-75550872020-10-19 Maturation of cortical microstructure and cognitive development in childhood and adolescence: A T1w/T2w ratio MRI study Norbom, Linn B. Rokicki, Jaroslav Alnæs, Dag Kaufmann, Tobias Doan, Nhat Trung Andreassen, Ole A. Westlye, Lars T. Tamnes, Christian K. Hum Brain Mapp Research Articles The restructuring and optimization of the cerebral cortex from early childhood and through adolescence is an essential feature of human brain development, underlying immense cognitive improvements. Beyond established morphometric cortical assessments, the T1w/T2w ratio quantifies partly separate biological processes, and might inform models of typical neurocognitive development and developmental psychopathology. In the present study, we computed vertex‐wise T1w/T2w ratio across the cortical surface in 621 youths (3–21 years) sampled from the Pediatric Imaging, Neurocognition, and Genetics (PING) study and tested for associations with individual differences in age, sex, and both general and specific cognitive abilities. The results showed a near global linear age‐related increase in T1w/T2w ratio across the brain surface, with a general posterior to anterior increasing gradient in association strength. Moreover, results indicated that boys in late adolescence had regionally higher T1w/T2w ratio as compared to girls. Across individuals, T1w/T2w ratio was negatively associated with general and several specific cognitive abilities mainly within anterior cortical regions. Our study indicates age‐related differences in T1w/T2w ratio throughout childhood, adolescence, and young adulthood, in line with the known protracted myelination of the cortex. Moreover, the study supports T1w/T2w ratio as a promising surrogate measure of individual differences in intracortical brain structure in neurodevelopment. John Wiley & Sons, Inc. 2020-08-03 /pmc/articles/PMC7555087/ /pubmed/32744409 http://dx.doi.org/10.1002/hbm.25149 Text en © 2020 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Norbom, Linn B.
Rokicki, Jaroslav
Alnæs, Dag
Kaufmann, Tobias
Doan, Nhat Trung
Andreassen, Ole A.
Westlye, Lars T.
Tamnes, Christian K.
Maturation of cortical microstructure and cognitive development in childhood and adolescence: A T1w/T2w ratio MRI study
title Maturation of cortical microstructure and cognitive development in childhood and adolescence: A T1w/T2w ratio MRI study
title_full Maturation of cortical microstructure and cognitive development in childhood and adolescence: A T1w/T2w ratio MRI study
title_fullStr Maturation of cortical microstructure and cognitive development in childhood and adolescence: A T1w/T2w ratio MRI study
title_full_unstemmed Maturation of cortical microstructure and cognitive development in childhood and adolescence: A T1w/T2w ratio MRI study
title_short Maturation of cortical microstructure and cognitive development in childhood and adolescence: A T1w/T2w ratio MRI study
title_sort maturation of cortical microstructure and cognitive development in childhood and adolescence: a t1w/t2w ratio mri study
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7555087/
https://www.ncbi.nlm.nih.gov/pubmed/32744409
http://dx.doi.org/10.1002/hbm.25149
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