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Tracking Development of the Corpus Callosum in Fetal and Early Postnatal Baboons Using Magnetic Resonance Imaging
Although the maturation of the corpus callosum (CC) can serve as a sensitive marker for normative antenatal and postnatal brain development, little is known about its development across this critical period. While high-resolution magnetic resonance imaging can provide an opportunity to examine norma...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bentham Open
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3256811/ https://www.ncbi.nlm.nih.gov/pubmed/22253660 http://dx.doi.org/10.2174/1874440001105010179 |
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author | Phillips, Kimberley A Kochunov, Peter |
author_facet | Phillips, Kimberley A Kochunov, Peter |
author_sort | Phillips, Kimberley A |
collection | PubMed |
description | Although the maturation of the corpus callosum (CC) can serve as a sensitive marker for normative antenatal and postnatal brain development, little is known about its development across this critical period. While high-resolution magnetic resonance imaging can provide an opportunity to examine normative brain development in humans, concerns remain over the exposure of developing fetuses to non-essential imaging. Nonhuman primates can provide a valuable model for normative brain maturation. Baboons share several important developmental characteristics with humans, including a highly orchestrated pattern of cerebral development. Developmental changes in total CC area and its subdivisions were examined across the antenatal (weeks 17 – 26 of 28 weeks total gestation) and early postnatal (to week 32) period in baboons (Papio hamadryas anubis). Thirteen fetal and sixteen infant baboons were studied using high-resolution MRI. During the period of primary gyrification, the total area of the CC increased by a magnitude of five. By postnatal week 32, the total CC area attained only 51% of the average adult area. CC subdivisions showed non-uniform increases in area, throughout development. The splenium showed the most maturation by postnatal week 32, attaining 55% of the average adult value. The subdivisions of the genu and anterior midbody showed the least maturation by postnatal week 32, attaining 50% and 49% of the average adult area. Thus, the CC of baboons shows continued growth past the postnatal period. These age-related changes in the developing baboon CC are consistent with the developmental course in humans. |
format | Online Article Text |
id | pubmed-3256811 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Bentham Open |
record_format | MEDLINE/PubMed |
spelling | pubmed-32568112012-01-17 Tracking Development of the Corpus Callosum in Fetal and Early Postnatal Baboons Using Magnetic Resonance Imaging Phillips, Kimberley A Kochunov, Peter Open Neuroimag J Article Although the maturation of the corpus callosum (CC) can serve as a sensitive marker for normative antenatal and postnatal brain development, little is known about its development across this critical period. While high-resolution magnetic resonance imaging can provide an opportunity to examine normative brain development in humans, concerns remain over the exposure of developing fetuses to non-essential imaging. Nonhuman primates can provide a valuable model for normative brain maturation. Baboons share several important developmental characteristics with humans, including a highly orchestrated pattern of cerebral development. Developmental changes in total CC area and its subdivisions were examined across the antenatal (weeks 17 – 26 of 28 weeks total gestation) and early postnatal (to week 32) period in baboons (Papio hamadryas anubis). Thirteen fetal and sixteen infant baboons were studied using high-resolution MRI. During the period of primary gyrification, the total area of the CC increased by a magnitude of five. By postnatal week 32, the total CC area attained only 51% of the average adult area. CC subdivisions showed non-uniform increases in area, throughout development. The splenium showed the most maturation by postnatal week 32, attaining 55% of the average adult value. The subdivisions of the genu and anterior midbody showed the least maturation by postnatal week 32, attaining 50% and 49% of the average adult area. Thus, the CC of baboons shows continued growth past the postnatal period. These age-related changes in the developing baboon CC are consistent with the developmental course in humans. Bentham Open 2011-11-18 /pmc/articles/PMC3256811/ /pubmed/22253660 http://dx.doi.org/10.2174/1874440001105010179 Text en © Phillips and Kochunov; Licensee Bentham Open. (http://creativecommons.org/-licenses/by-nc/3.0/ This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/-licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited. |
spellingShingle | Article Phillips, Kimberley A Kochunov, Peter Tracking Development of the Corpus Callosum in Fetal and Early Postnatal Baboons Using Magnetic Resonance Imaging |
title | Tracking Development of the Corpus Callosum in Fetal and Early Postnatal Baboons Using Magnetic Resonance Imaging |
title_full | Tracking Development of the Corpus Callosum in Fetal and Early Postnatal Baboons Using Magnetic Resonance Imaging |
title_fullStr | Tracking Development of the Corpus Callosum in Fetal and Early Postnatal Baboons Using Magnetic Resonance Imaging |
title_full_unstemmed | Tracking Development of the Corpus Callosum in Fetal and Early Postnatal Baboons Using Magnetic Resonance Imaging |
title_short | Tracking Development of the Corpus Callosum in Fetal and Early Postnatal Baboons Using Magnetic Resonance Imaging |
title_sort | tracking development of the corpus callosum in fetal and early postnatal baboons using magnetic resonance imaging |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3256811/ https://www.ncbi.nlm.nih.gov/pubmed/22253660 http://dx.doi.org/10.2174/1874440001105010179 |
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