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EDITORIAL article

Front. Neurosci., 06 February 2023
Sec. Neurodevelopment
This article is part of the Research Topic Imaging the Developing Connectome of Perinatal Brain View all 10 articles

Editorial: Imaging the developing connectome of perinatal brain

  • 1Key Laboratory for Biomedical Engineering of Ministry of Education, College of Biomedical Engineering and Instrument Science, Zhejiang University, Hangzhou, China
  • 2Gansu Provincial Key Laboratory for Wearable Computing, School of Information Science and Engineering, Lanzhou University, Lanzhou, China
  • 3Fetal Neonatal Neuroimaging and Developmental Science Center, Boston Children's Hospital, Boston, MA, United States
  • 4Division of Newborn Medicine, Boston Children's Hospital, Boston, MA, United States
  • 5Department of Radiology, Boston Children's Hospital, Boston, MA, United States
  • 6Department of Pediatrics, Harvard Medical School, Boston, MA, United States
  • 7Department of Radiology, Children's Hospital of Philadelphia, Philadelphia, PA, United States
  • 8Department of Radiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States

Brain maturation during the perinatal period in the fetus and infant is a rapid and complex process. Neurodevelopment during this period is critical for supporting later cognitive, emotional, and behavioral abilities. Increasing evidence for the perinatal origins of various neurodevelopmental disorders underscores the importance of identifying features of early brain development (Dehaene-Lambertz and Spelke, 2015). Understanding the developing brain connectome will open new insights into the fundamental processes of brain circuit formation and maturation in early life and reveal the etiology of intractable neurodevelopmental disorders. Advances in magnetic resonance imaging (MRI), such as rapid imaging and motion correction techniques, have overcome significant challenges in fetal and infant brain MRI and enabled non-invasive in vivo assessment of functional and structural connectivity between separate brain regions (Kaiser, 2017; Dubois et al., 2021), offering great opportunities to capture the connectome of the fetal and postnatal brain with unprecedented accuracy. Thus, the purpose of this Research Topic focuses on neuroimaging studies of the early development of the brain connectome.

This Research Topic includes 8 original research paper and 1 data descriptor. Main research contents concentrate on atypical connectome pattern and novel imaging biomarkers for prematurity, hypoxic ischemic encephalopathy (HIE), etc. and machine learning algorithms for fetal brain analysis. Neumane et al. explored the impact of prematurity on the development and integrity of the sensorimotor connectivity and their relationship to later motor impairments. They found that prematurity affected early microstructural development of the primary sensorimotor network and these effects differed according to the level of prematurity. They also highlighted the microstructural development of specific tracts predicted fine motor and cognitive outcomes at 18 months. Li et al. investigated the effects of daily iron supplementation on motor development and brain structural connectivity of preterm infants. They found that iron status at early postnatal period was related to both motor development and connectivity decreases, and the delayed motor development can be reversed by supplying 2 mg/kg of iron per day for 6 months. Vishnubhotla et al. studied the influence of prenatal opioid exposure on brain structural connectivity, and identified two connectivity pathways that were significantly differed between opioid exposure infants and unexposed controls. Votava-Smith et al. reported that clinical risk factors and brain dysplasia score were associated with distinct brain dysmaturation patterns in term neonates with congenital heart disease (CHD). Specifically, clinical factors were most predictive to postnatal microstructural dysmaturation, whereas subcortical dysplasia predicted connectome-based measures, suggesting the complementary effects of connectome and microstructure in deciphering risk factors related to poor neurodevelopment in CHD. Based on the least absolute shrinkage and selection operator (LASSO) regression model, Onda et al. developed a novel biomarker named composite diffusion tensor imaging (cDTI) score to assess the severity of short-term neurological functions of HIE neonates. They demonstrated high cDTI scores were related to the intensity of the early inflammatory response and the severity of neuronal impairment after therapeutic hypothermia.

Characterizing fetal brain development in utero is still challenging due to the difficulties in acquiring high-quality MRI data and lack of effective analytic methods. Based on 188 brain MRI of normal fetuses ranging from 19 to 37 gestational weeks, Ren et al. establish a reference of intracranial structure volumes during this period by manual segmentation from two experienced experts. Wang et al. developed a MRI-based semi-automatic pipeline to segment the cortex and subcortical structures of fetal brains, reducing the costs of manual segmentation. De Asis-Cruz et al. proposed a full automatic and computationally efficient generative adversarial neural network for segmenting the fetal brain based on functional MRI, which yielded whole brain masks that closely approximated the manually labeled ground truth. This study is of great significance in facilitating in utero investigations of emerging functional connectivity.

Lack of available and reliable data is one of dominating factors that limits the exploration of brain maturational trajectories early in life. Edwards et al. introduced the neonatal data release of the Developing Human Connectome Project, which includes 887 multimodal high-quality MR images from 783 preterm-born and term-born infants and essential metadata. This open dataset allows researchers to design the experiment as they wish, making great contribution to uncover the typical and atypical brain development across the perinatal period.

In conclusion, these nine papers included in this Research Topic summary the recent progression of normal brain maturation and markers of neurodevelopmental disorders during the perinatal period, as well as important technical advances in fetal and infantile brain MRI.

Author contributions

All authors listed have made a substantial, direct, and intellectual contribution to the work and approved it for publication.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

Dehaene-Lambertz, G., and Spelke, E. S. (2015). The infancy of the human brain. Neuron 88, 93–109. doi: 10.1016/j.neuron.2015.09.026

PubMed Abstract | CrossRef Full Text | Google Scholar

Dubois, J., Alison, M., Counsell, S. J., Hertz-Pannier, L., Hüppi, P. S., and Benders, M. (2021). MRI of the neonatal brain: a review of methodological challenges and neuroscientific advances. J. Magn. Reson. Imag. JMRI 53, 1318–1343. doi: 10.1002/jmri.27192

PubMed Abstract | CrossRef Full Text | Google Scholar

Kaiser, M. (2017). Mechanisms of connectome development. Trends Cogn. Sci. 21, 703–717. doi: 10.1016/j.tics.2017.05.010

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: magnetic resonance imaging (MRI), perinatal brain, connectome, imaging biomarkers, development, analytic methods

Citation: Wu D, Zheng W, Grant PE and Huang H (2023) Editorial: Imaging the developing connectome of perinatal brain. Front. Neurosci. 17:1122829. doi: 10.3389/fnins.2023.1122829

Received: 13 December 2022; Accepted: 25 January 2023;
Published: 06 February 2023.

Edited and reviewed by: Dustin Scheinost, Yale University, United States

Copyright © 2023 Wu, Zheng, Grant and Huang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Dan Wu, yes danwu.bme@zju.edu.cn; Weihao Zheng, yes zhengweihao@lzu.edu.cn

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.