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Development of human white matter pathways in utero over the second and third trimester.
Wilson, Siân; Pietsch, Maximilian; Cordero-Grande, Lucilio; Price, Anthony N; Hutter, Jana; Xiao, Jiaxin; McCabe, Laura; Rutherford, Mary A; Hughes, Emer J; Counsell, Serena J; Tournier, Jacques-Donald; Arichi, Tomoki; Hajnal, Joseph V; Edwards, A David; Christiaens, Daan; O'Muircheartaigh, Jonathan.
Afiliação
  • Wilson S; Centre for the Developing Brain, School of Biomedical Engineering and Imaging Sciences, King's College London, London, SE1 7EH, United Kingdom.
  • Pietsch M; Centre for Neurodevelopmental Disorders, Kings College London, London, SE1 1UL, United Kingdom.
  • Cordero-Grande L; Centre for the Developing Brain, School of Biomedical Engineering and Imaging Sciences, King's College London, London, SE1 7EH, United Kingdom.
  • Price AN; Centre for the Developing Brain, School of Biomedical Engineering and Imaging Sciences, King's College London, London, SE1 7EH, United Kingdom.
  • Hutter J; Biomedical Image Technologies, ETSI Telecomunicación, Universidad Politécnica de Madrid, 28040 Madrid, Spain.
  • Xiao J; Biomedical Research Networking Center in Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN), 28029 Madrid, Spain.
  • McCabe L; Centre for the Developing Brain, School of Biomedical Engineering and Imaging Sciences, King's College London, London, SE1 7EH, United Kingdom.
  • Rutherford MA; Centre for the Developing Brain, School of Biomedical Engineering and Imaging Sciences, King's College London, London, SE1 7EH, United Kingdom.
  • Hughes EJ; Centre for the Developing Brain, School of Biomedical Engineering and Imaging Sciences, King's College London, London, SE1 7EH, United Kingdom.
  • Counsell SJ; Centre for the Developing Brain, School of Biomedical Engineering and Imaging Sciences, King's College London, London, SE1 7EH, United Kingdom.
  • Tournier JD; Centre for the Developing Brain, School of Biomedical Engineering and Imaging Sciences, King's College London, London, SE1 7EH, United Kingdom.
  • Arichi T; Centre for the Developing Brain, School of Biomedical Engineering and Imaging Sciences, King's College London, London, SE1 7EH, United Kingdom.
  • Hajnal JV; Centre for the Developing Brain, School of Biomedical Engineering and Imaging Sciences, King's College London, London, SE1 7EH, United Kingdom.
  • Edwards AD; Centre for the Developing Brain, School of Biomedical Engineering and Imaging Sciences, King's College London, London, SE1 7EH, United Kingdom.
  • Christiaens D; Centre for the Developing Brain, School of Biomedical Engineering and Imaging Sciences, King's College London, London, SE1 7EH, United Kingdom; tomoki.arichi@kcl.ac.uk.
  • O'Muircheartaigh J; Children's Neurosciences, Evelina London Children's Hospital, Guy's and St Thomas' NHS Foundation Trust, London SE1 7EH, United Kingdom.
Proc Natl Acad Sci U S A ; 118(20)2021 05 18.
Article em En | MEDLINE | ID: mdl-33972435
ABSTRACT
During the second and third trimesters of human gestation, rapid neurodevelopment is underpinned by fundamental processes including neuronal migration, cellular organization, cortical layering, and myelination. In this time, white matter growth and maturation lay the foundation for an efficient network of structural connections. Detailed knowledge about this developmental trajectory in the healthy human fetal brain is limited, in part, due to the inherent challenges of acquiring high-quality MRI data from this population. Here, we use state-of-the-art high-resolution multishell motion-corrected diffusion-weighted MRI (dMRI), collected as part of the developing Human Connectome Project (dHCP), to characterize the in utero maturation of white matter microstructure in 113 fetuses aged 22 to 37 wk gestation. We define five major white matter bundles and characterize their microstructural features using both traditional diffusion tensor and multishell multitissue models. We found unique maturational trends in thalamocortical fibers compared with association tracts and identified different maturational trends within specific sections of the corpus callosum. While linear maturational increases in fractional anisotropy were seen in the splenium of the corpus callosum, complex nonlinear trends were seen in the majority of other white matter tracts, with an initial decrease in fractional anisotropy in early gestation followed by a later increase. The latter is of particular interest as it differs markedly from the trends previously described in ex utero preterm infants, suggesting that this normative fetal data can provide significant insights into the abnormalities in connectivity which underlie the neurodevelopmental impairments associated with preterm birth.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tálamo / Córtex Cerebral / Corpo Caloso / Desenvolvimento Fetal / Substância Branca Limite: Female / Humans / Infant / Newborn / Pregnancy Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tálamo / Córtex Cerebral / Corpo Caloso / Desenvolvimento Fetal / Substância Branca Limite: Female / Humans / Infant / Newborn / Pregnancy Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Reino Unido