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Objective: Diffusion tensor imaging (DTI) of the fetal brain can generate unique quantitative data that reflect both tissue integrity and the level of myelination in the developing brain. The objective of this study was to quantify normal fetal brain metrics from 21 to 36 weeks' gestation using DTI in a cohort of healthy fetuses, using the latest techniques designed to minimize artifacts from movement and those inherent to magnetic resonance imaging (MRI) acquisition.
Methods: We conducted a prospective study between June 2021 and June 2022 of pregnant volunteers with no known fetal anomalies, between 21 and 36 weeks' gestation. MRI scans were performed using a 1.5-T 450W General Electric Signa MRI system, including 15 non-collinear diffusion-weighted axial images of the fetal brain. Preprocessing included denoising, correction of Gibb's ringing artifact, eddy current correction, bias removal, registration to a reference template, slice-to-volume reconstruction and constrained spherical convolution to obtain maps of fractional anisotropy (FA), apparent diffusion coefficient (ADC), axial diffusivity (AD) and radial diffusivity (RD). A total of 51 white matter and gray matter regions from both hemispheres were analyzed. Regression models were used to describe the evolution of the DTI metrics during gestation.
Results: DTI was successful in 94/111 (84.7%) fetuses and was performed at a median of 30 (range, 21-36) weeks' gestation. In the different white matter tracts, FA showed five distinct patterns: (1) initial decrease until 32-34 weeks, followed by an increase until 36 weeks; (2) initial decrease until 25-26 weeks, followed by an increase until 36 weeks; (3) linear increase; (4) linear decrease; or (5) no gestational-age-related change. In the different gray matter regions, FA showed three distinct patterns: (1) linear decrease; (2) initial decrease until 31-34 weeks, followed by an increase; or (3) no gestational-age-related change. In the majority of white matter and gray matter regions, ADC, AD and RD showed a linear decrease between 21 and 36 weeks.
Conclusions: The variations in DTI metrics may indirectly reflect the microstructural changes that occur during brain development, particularly during myelination, and may help characterize the development of fetal brain connectivity in utero. © 2025 International Society of Ultrasound in Obstetrics and Gynecology.
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http://dx.doi.org/10.1002/uog.29275 | DOI Listing |
This manuscript explores the myriad ethical controversies associated with declaration of brain death/death by neurologic criteria (BD/DNC) during pregnancy raised by the case of Ms. Adriana Smith, a 30-year-old Georgia nurse, who came to international attention in May 2025. We will discuss: (1) the factors that may have impacted the decision not to perform neuroimaging when she first presented to medical attention; (2) the significance of identifying and deferring performance of futile interventions to decrease intracranial pressure relative to BD/DNC declaration; (3) the medical, ethical and legal complexities associated with BD/DNC declaration and continuation of maternal organ support in pregnancy; (4) the impact of continuing maternal organ support after BD/DNC declaration on the fetus, the family, Ms.
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Division of Animal Sciences, University of Missouri, 920 East Campus Drive, Columbia, Missouri 65211, USA.
Mice lacking caveolin-1 (), a major protein of the lipid raft of plasma membrane, show deregulated cellular proliferation of the mammary gland and an abnormal fetoplacental communication during pregnancy. This study leverages a multi-omics approach to test the hypothesis that the absence of elicits a coordinated crosstalk of genes among the mammary gland, placenta and fetal brain in pregnant mice. Integrative analysis of metabolomics and transcriptomics data of mammary glands showed that the loss of significantly impacted specific metabolites and metabolic pathways in the pregnant mice.
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Division of Neonatology, Department of Pediatrics, Willem-Alexander Children's Hospital, Leiden University Medical Center, the Netherlands. (B.O.v.O., M.R., M.S.S., E.L., L.S.d.V., S.J.S.).
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Laboratory of Fetal Neuroprogramming, Institute of Health Sciences, University of O'Higgins, Rancagua, Chile.
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