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Intrinsic Functional Brain Architecture Derived from Graph Theoretical Analysis in the Human Fetus
The human brain undergoes dramatic maturational changes during late stages of fetal and early postnatal life. The importance of this period to the establishment of healthy neural connectivity is apparent in the high incidence of neural injury in preterm infants, in whom untimely exposure to ex-uteri...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4006774/ https://www.ncbi.nlm.nih.gov/pubmed/24788455 http://dx.doi.org/10.1371/journal.pone.0094423 |
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author | Thomason, Moriah E. Brown, Jesse A. Dassanayake, Maya T. Shastri, Rupal Marusak, Hilary A. Hernandez-Andrade, Edgar Yeo, Lami Mody, Swati Berman, Susan Hassan, Sonia S. Romero, Roberto |
author_facet | Thomason, Moriah E. Brown, Jesse A. Dassanayake, Maya T. Shastri, Rupal Marusak, Hilary A. Hernandez-Andrade, Edgar Yeo, Lami Mody, Swati Berman, Susan Hassan, Sonia S. Romero, Roberto |
author_sort | Thomason, Moriah E. |
collection | PubMed |
description | The human brain undergoes dramatic maturational changes during late stages of fetal and early postnatal life. The importance of this period to the establishment of healthy neural connectivity is apparent in the high incidence of neural injury in preterm infants, in whom untimely exposure to ex-uterine factors interrupts neural connectivity. Though the relevance of this period to human neuroscience is apparent, little is known about functional neural networks in human fetal life. Here, we apply graph theoretical analysis to examine human fetal brain connectivity. Utilizing resting state functional magnetic resonance imaging (fMRI) data from 33 healthy human fetuses, 19 to 39 weeks gestational age (GA), our analyses reveal that the human fetal brain has modular organization and modules overlap functional systems observed postnatally. Age-related differences between younger (GA <31 weeks) and older (GA≥31 weeks) fetuses demonstrate that brain modularity decreases, and connectivity of the posterior cingulate to other brain networks becomes more negative, with advancing GA. By mimicking functional principles observed postnatally, these results support early emerging capacity for information processing in the human fetal brain. Current technical limitations, as well as the potential for fetal fMRI to one day produce major discoveries about fetal origins or antecedents of neural injury or disease are discussed. |
format | Online Article Text |
id | pubmed-4006774 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-40067742014-05-09 Intrinsic Functional Brain Architecture Derived from Graph Theoretical Analysis in the Human Fetus Thomason, Moriah E. Brown, Jesse A. Dassanayake, Maya T. Shastri, Rupal Marusak, Hilary A. Hernandez-Andrade, Edgar Yeo, Lami Mody, Swati Berman, Susan Hassan, Sonia S. Romero, Roberto PLoS One Research Article The human brain undergoes dramatic maturational changes during late stages of fetal and early postnatal life. The importance of this period to the establishment of healthy neural connectivity is apparent in the high incidence of neural injury in preterm infants, in whom untimely exposure to ex-uterine factors interrupts neural connectivity. Though the relevance of this period to human neuroscience is apparent, little is known about functional neural networks in human fetal life. Here, we apply graph theoretical analysis to examine human fetal brain connectivity. Utilizing resting state functional magnetic resonance imaging (fMRI) data from 33 healthy human fetuses, 19 to 39 weeks gestational age (GA), our analyses reveal that the human fetal brain has modular organization and modules overlap functional systems observed postnatally. Age-related differences between younger (GA <31 weeks) and older (GA≥31 weeks) fetuses demonstrate that brain modularity decreases, and connectivity of the posterior cingulate to other brain networks becomes more negative, with advancing GA. By mimicking functional principles observed postnatally, these results support early emerging capacity for information processing in the human fetal brain. Current technical limitations, as well as the potential for fetal fMRI to one day produce major discoveries about fetal origins or antecedents of neural injury or disease are discussed. Public Library of Science 2014-05-01 /pmc/articles/PMC4006774/ /pubmed/24788455 http://dx.doi.org/10.1371/journal.pone.0094423 Text en © 2014 Thomason et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Thomason, Moriah E. Brown, Jesse A. Dassanayake, Maya T. Shastri, Rupal Marusak, Hilary A. Hernandez-Andrade, Edgar Yeo, Lami Mody, Swati Berman, Susan Hassan, Sonia S. Romero, Roberto Intrinsic Functional Brain Architecture Derived from Graph Theoretical Analysis in the Human Fetus |
title | Intrinsic Functional Brain Architecture Derived from Graph Theoretical Analysis in the Human Fetus |
title_full | Intrinsic Functional Brain Architecture Derived from Graph Theoretical Analysis in the Human Fetus |
title_fullStr | Intrinsic Functional Brain Architecture Derived from Graph Theoretical Analysis in the Human Fetus |
title_full_unstemmed | Intrinsic Functional Brain Architecture Derived from Graph Theoretical Analysis in the Human Fetus |
title_short | Intrinsic Functional Brain Architecture Derived from Graph Theoretical Analysis in the Human Fetus |
title_sort | intrinsic functional brain architecture derived from graph theoretical analysis in the human fetus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4006774/ https://www.ncbi.nlm.nih.gov/pubmed/24788455 http://dx.doi.org/10.1371/journal.pone.0094423 |
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