Exploring early human brain development with structural and physiological neuroimaging
Open accessAbstract
Early brain development, from the embryonic period to infancy, is characterized by rapid structural and functional changes. These changes can be studied using structural and physiological neuroimaging methods. In order to optimally acquire and accurately interpret this data, concepts from adult neuroimaging cannot be directly transferred. Instead, one must have a basic understanding of fetal and neonatal structural and physiological brain development, and the important modulators of this process. Here, we first review the major developmental milestones of transient cerebral structures and structural connectivity (axonal connectivity) followed by a summary of the contributions from ex vivo and in vivo MRI. Next, we discuss the basic biology of neuronal circuitry development (synaptic connectivity, i.e. ensemble of direct chemical and electrical connections between neurons), physiology of neurovascular coupling, baseline metabolic needs of the fetus and the infant, and functional connectivity (defined as statistical dependence of low-frequency spontaneous fluctuations seen with functional magnetic resonance imaging (fMRI)). The complementary roles of magnetic resonance imaging (MRI), electroencephalography (EEG), magnetoencephalography (MEG), and near-infrared spectroscopy (NIRS) are discussed. We include a section on modulators of brain development where we focus on the placenta and emerging placental MRI approaches. In each section we discuss key technical limitations of the imaging modalities and some of the limitations arising due to the biology of the system. Although neuroimaging approaches have contributed significantly to our understanding of early brain development, there is much yet to be done and a dire need for technical innovations and scientific discoveries to realize the future potential of early fetal and infant interventions to avert long term disease.
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Significant differences between the adult and fetal BOLD response may be equally as likely.
“Nevertheless, with all the ongoing changes in the developing brain (e.g., angiogenesis, neurogenesis, synaptic formation, etc.), significant differences between the adult and fetal BOLD response may be equally as likely [84].”
From Brain structural and functional outcomes in the offspring of women experiencing psychological distress during pregnancy (2024) · cites this paper as [84]
The “Vasculogenesis and the development of neurovascular coupling” section says fMRI responses depend on neurovascular development and that the fetal vascular response remains unclear. This supports the possibility of a fetal response differing from an adult one, but it does not assess whether a significant difference is equally likely. (LLM, conf=0.78)
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References 478 · Cited by 177
Research works printed but not linked: 5
- Chao Y, Yeh C, Cho K, Chen J, Lin C, 2007 Multiple streamline tractography approach with high angular resolution diffusion imaging data. Proceedings of the international society of magnetic resonance in medicine 1550.
- Luo J, Gagoski B, Abaci Turk E, Yang J, Copeland N, Roberts D, Zhou I, Grant P, 2017b Feasibility of glucose CEST in the human placenta. In: Annual Proceedings of the International Society for Magnetic Resonance in Medicine (Honolulu).
- O’Rahilly RR, Müller F, 2006 The Embryonic Human Brain: anAtlas ofDevelopmental Stages. John Wiley & Sons.
- Ponrartana S, Devaskar S, Chia J, Rajagopolan V, Lai H, Miller D, Gilsanz V, 2015 Intravoxel incoherent motion diffusion-weighted MR imaging of the placenta: evaluation of perfusion changes in the supine and left lateral decubitus positions. In: 23rd Annual Proceedings of the International Society for Magnetic Resonance in Medicine (Toronto, Ontario).
- Rathi Y, Niethammer M, Laun F, Setsompop K, Michailovich O, Grant PE, Westin C-F, 2014 Diffusion Propagator Estimation Using Radial Basis Functions Computational Diffusion MRI and Brain Connectivity. Springer, pp. 57– 66.
- Authors
- Vasung, L., Abaci Turk, E., Ferradal, S. L., Sutin, J., Stout, J. N., Ahtam, B., Lin, P.-Y., & Grant, P. E.
- Affiliations
- Boston Children's Hospital (US)
- Corresponding author
- Grant, P. Ellen
- ORCID
- Venue
- NeuroImage
- Publisher
- Elsevier BV
- Published
- 2019-02
- Volume
- 187
- Pages
- 226-254
- ISSN
- 1053-8119 (ISSN-L)
- PMC
- PMC6537870
- OpenAlex
- W2884551766
- Cited by
- 177
- References
- 478
- Citations by year
- 2026: 11 · 2025: 24 · 2024: 32 · 2023: 24 · 2022: 35 · 2021: 27 · 2020: 18 · 2019: 4 · 2018: 2
- FWCI
- 2.44
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- NeuroImage (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (U01NS082320, R01MH097979, R01HD076258, R01EB017337, R01HD078561, R01HD079484, U01HD087211, R21HD083956, HD065762, R01HL135061, DP1HD091947, R00HD083512)
- SNSF (P300PB_167804)
- Topics
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Fetal and Pediatric Neurological Disorders
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced MRI Techniques and Applications
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
- Keywords
- early brain development, fetal brain development, neonatal brain development, axonal connectivity, structural connectivity, fetal MRI, neonatal MRI, synaptic connectivity, neurovascular coupling, functional connectivity, spontaneous neural fluctuations, placenta, placental MRI
- MeSH terms
- Neurovascular Coupling, Brain, Brain Mapping, Female, Gestational Age, Humans, Infant, Neural Pathways, Pregnancy, Neuroimaging, White Matter
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