Characterizing microstructural development in the fetal brain using diffusion MRI from 23 to 36 weeks of gestation

Author:

Calixto Camilo123ORCID,Machado-Rivas Fedel34,Cortes-Albornoz Maria C34,Karimi Davood123,Velasco-Annis Clemente123,Afacan Onur123,Warfield Simon K123,Gholipour Ali123,Jaimes Camilo34

Affiliation:

1. Computational Radiology Laboratory , Department of Radiology, , Boston, MA 02115 , United States

2. Boston Children’s Hospital , Department of Radiology, , Boston, MA 02115 , United States

3. Department of Radiology, Harvard Medical School , Boston, MA 02115 , United States

4. Department of Radiology, Massachusetts General Hospital , Boston, MA 02114 , United States

Abstract

Abstract We utilized motion-corrected diffusion tensor imaging (DTI) to evaluate microstructural changes in healthy fetal brains during the late second and third trimesters. Data were derived from fetal magnetic resonance imaging scans conducted as part of a prospective study spanning from 2013 March to 2019 May. The study included 44 fetuses between the gestational ages (GAs) of 23 and 36 weeks. We reconstructed fetal brain DTI using a motion-tracked slice-to-volume registration framework. Images were segmented into 14 regions of interest (ROIs) through label propagation using a fetal DTI atlas, with expert refinement. Statistical analysis involved assessing changes in fractional anisotropy (FA) and mean diffusivity (MD) throughout gestation using mixed-effects models, and identifying points of change in trajectory for ROIs with nonlinear trends. Results showed significant GA-related changes in FA and MD in all ROIs except in the thalamus’ FA and corpus callosum’s MD. Hemispheric asymmetries were found in the FA of the periventricular white matter (pvWM), intermediate zone, and subplate and in the MD of the ganglionic eminence and pvWM. This study provides valuable insight into the normal patterns of development of MD and FA in the fetal brain. These changes are closely linked with cytoarchitectonic changes and display indications of early functional specialization.

Funder

National Institute of Biomedical Imaging and Bioengineering

National Institute of Neurological Disorders and Stroke

U.S. National Library of Medicine

Eunice Kennedy Shriver National Institute of Child Health and Human Development

National Institutes of Health

NIH Office of the Director

National Science Foundation

Rosamund Stone Zander Translational Neuroscience Center

Boston Children's Hospital

American Roentgen Ray Society

Office of Faculty Development at Boston Children’s Hospital

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience

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