Myelin Water Fraction Imaging of the Brain in Children with Prenatal Alcohol Exposure.


Journal

Alcoholism, clinical and experimental research
ISSN: 1530-0277
Titre abrégé: Alcohol Clin Exp Res
Pays: England
ID NLM: 7707242

Informations de publication

Date de publication:
05 2019
Historique:
received: 13 12 2018
accepted: 10 03 2019
pubmed: 20 3 2019
medline: 3 7 2020
entrez: 20 3 2019
Statut: ppublish

Résumé

Prenatal alcohol exposure (PAE) is linked to alterations of cerebral white matter, including volume and nonspecific diffusion magnetic resonance imaging (MRI) indices of microstructure in humans. Some animal models of PAE have demonstrated myelination deficiencies, but myelin levels have not yet been evaluated in individuals with PAE. Multiecho T Participants with PAE (n = 10, 6 females, mean age 13.9 years, range 7 to 18 years) and controls (n = 14, 11 females, mean age 13.2 years, range 9 to 16 years) underwent 3T MRI of the brain. T As expected, across the combined sample, MWF was highest for major white matter tracts such as the internal capsule and genu/splenium of the corpus callosum (10 to 18%) while the caudate and putamen had MWF less than 5%. Mean MWF was similar across 11/12 brain white and gray matter regions for the PAE and control groups (L/R internal capsule, major forceps, putamen, caudate nucleus, L minor forceps, genu and splenium of corpus callosum). In the PAE group, MWF was positively correlated with age in the genu of corpus callosum and right minor forceps, notably 2 frontal tracts. Given comparable MRI-derived myelination fraction measures in PAE relative to controls, white matter alterations shown in other imaging studies, such as diffusion tensor imaging, may reflect microstructural anomalies related to axon caliber and density.

Sections du résumé

BACKGROUND
Prenatal alcohol exposure (PAE) is linked to alterations of cerebral white matter, including volume and nonspecific diffusion magnetic resonance imaging (MRI) indices of microstructure in humans. Some animal models of PAE have demonstrated myelination deficiencies, but myelin levels have not yet been evaluated in individuals with PAE. Multiecho T
METHODS
Participants with PAE (n = 10, 6 females, mean age 13.9 years, range 7 to 18 years) and controls (n = 14, 11 females, mean age 13.2 years, range 9 to 16 years) underwent 3T MRI of the brain. T
RESULTS
As expected, across the combined sample, MWF was highest for major white matter tracts such as the internal capsule and genu/splenium of the corpus callosum (10 to 18%) while the caudate and putamen had MWF less than 5%. Mean MWF was similar across 11/12 brain white and gray matter regions for the PAE and control groups (L/R internal capsule, major forceps, putamen, caudate nucleus, L minor forceps, genu and splenium of corpus callosum). In the PAE group, MWF was positively correlated with age in the genu of corpus callosum and right minor forceps, notably 2 frontal tracts.
CONCLUSIONS
Given comparable MRI-derived myelination fraction measures in PAE relative to controls, white matter alterations shown in other imaging studies, such as diffusion tensor imaging, may reflect microstructural anomalies related to axon caliber and density.

Identifiants

pubmed: 30889291
doi: 10.1111/acer.14024
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

833-841

Subventions

Organisme : Kids Brain Health Network
Pays : International
Organisme : Alberta Innovates Health Solutions
Pays : International
Organisme : Women's and Children's Health Research Institute
Pays : International
Organisme : Sunny Hill Health Centre Children's Foundation
Pays : International
Organisme : Canada Research Chairs
Pays : International

Informations de copyright

© 2019 by the Research Society on Alcoholism.

Auteurs

Kaitlyn McLachlan (K)

Department of Psychology , University of Guelph, Guelph, ON, Canada.

Irene Vavasour (I)

Department of Radiology , University of British Columbia, Vancouver, BC, Canada.

Alex MacKay (A)

Department of Radiology , University of British Columbia, Vancouver, BC, Canada.
Department of Physics and Astronomy , University of British Columbia, Vancouver, BC, Canada.

Ursula Brain (U)

Department of Pediatrics , University of British Columbia, Vancouver, BC, Canada.

Tim Oberlander (T)

Department of Pediatrics , University of British Columbia, Vancouver, BC, Canada.

Christine Loock (C)

Department of Pediatrics , University of British Columbia, Vancouver, BC, Canada.

James N Reynolds (JN)

Department of Biomedical and Molecular Sciences , Queens University, Kingston, ON, Canada.

Christian Beaulieu (C)

Department of Biomedical Engineering , University of Alberta, Edmonton, AB, Canada.

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