Literature DB >> 21575012

Extensive deep gray matter volume reductions in children and adolescents with fetal alcohol spectrum disorders.

Alexa Nardelli1, Catherine Lebel, Carmen Rasmussen, Gail Andrew, Christian Beaulieu.   

Abstract

BACKGROUND: The link between the numerous cognitive, motor, and behavioral difficulties of individuals with fetal alcohol spectrum disorders (FASD) and underlying specific structural brain injuries can be investigated using high-resolution imaging. Differential sensitivity of the brain's "relay" stations, namely the deep gray matter structures, may play a key factor given their multifaceted role in brain function. The purpose of our study was to analyze differences in deep gray matter volumes of children and adolescents with FASD relative to age/sex-matched controls and to examine whether any volume differences were consistent across the age range of neurodevelopment.
METHODS: Children and adolescents (N = 28, 6 to 17 years) diagnosed with FASD and 56 age- and sex-matched healthy controls (i.e., 2 matched controls per FASD subject) underwent 3-dimensional T1-weighted MRI scans that were used for the automated volume measurement (FreeSurfer) of the intracranial space, total white matter, cortical gray matter, and 6 deep gray matter structures, namely the hippocampus, amygdala, thalamus, caudate, putamen, and globus pallidus, with left and right measured separately. Volumes were compared between FASD and controls, as well as changes with age.
RESULTS: Significant reductions of volume in FASD were observed for the intracranial vault (7.6%), total white matter (8.6%), total cortical gray matter (7.8%), and total deep gray matter (13.1%). All 6 deep gray matter structures showed significant volume reductions bilaterally with the caudate (approximately 16%) and globus pallidus (approximately 18%) being most affected. The hippocampus, thalamus, and globus pallidus showed reductions in all 3 age subgroups (6 to 9, 10 to 13, and 14 to 17 years) but the caudate and putamen had smaller volumes for FASD only within the 2 youngest subgroups; the amygdala was only smaller for FASD in the 2 oldest subgroups.
CONCLUSIONS: Significant, but variable, volume reductions throughout the deep gray matter are observed over a wide age range of 6 to 17 years in FASD.
Copyright © 2011 by the Research Society on Alcoholism.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21575012     DOI: 10.1111/j.1530-0277.2011.01476.x

Source DB:  PubMed          Journal:  Alcohol Clin Exp Res        ISSN: 0145-6008            Impact factor:   3.455


  74 in total

1.  Differences in cortico-striatal-cerebellar activation during working memory in syndromal and nonsyndromal children with prenatal alcohol exposure.

Authors:  Vaibhav A Diwadkar; Ernesta M Meintjes; Dhruman Goradia; Neil C Dodge; Christopher Warton; Christopher D Molteno; Sandra W Jacobson; Joseph L Jacobson
Journal:  Hum Brain Mapp       Date:  2012-03-25       Impact factor: 5.038

Review 2.  Fetal Alcohol Spectrum Disorders: A Review of the Neurobehavioral Deficits Associated With Prenatal Alcohol Exposure.

Authors:  Sarah N Mattson; Gemma A Bernes; Lauren R Doyle
Journal:  Alcohol Clin Exp Res       Date:  2019-05-02       Impact factor: 3.455

3.  Differentiating the Effects of Familial Risk for Alcohol Dependence and Prenatal Exposure to Alcohol on Offspring Brain Morphology.

Authors:  Vinod K Sharma; Shirley Y Hill
Journal:  Alcohol Clin Exp Res       Date:  2017-01-13       Impact factor: 3.455

4.  Para-limbic Structural Abnormalities Are Associated With Internalizing Symptoms in Children With Prenatal Alcohol Exposure.

Authors:  Alyssa M Krueger; Donovan J Roediger; Bryon A Mueller; Christopher A Boys; Timothy J Hendrickson; Mariah J Schumacher; Sarah N Mattson; Kenneth L Jones; Edward P Riley; Kelvin O Lim; Jeffrey R Wozniak
Journal:  Alcohol Clin Exp Res       Date:  2020-07-01       Impact factor: 3.455

5.  Glucocorticoid receptor expression in the stress-limbic circuitry is differentially affected by prenatal alcohol exposure and adolescent stress.

Authors:  Charlis Raineki; Erin J Morgan; Linda Ellis; Joanne Weinberg
Journal:  Brain Res       Date:  2019-05-15       Impact factor: 3.252

6.  Children with Heavy Prenatal Alcohol Exposure Exhibit Atypical Gait Characteristics.

Authors:  Tenille C Taggart; Roger W Simmons; Jennifer D Thomas; Edward P Riley
Journal:  Alcohol Clin Exp Res       Date:  2017-08-21       Impact factor: 3.455

7.  DNA Methylation program in normal and alcohol-induced thinning cortex.

Authors:  Nail Can Öztürk; Marisol Resendiz; Hakan Öztürk; Feng C Zhou
Journal:  Alcohol       Date:  2017-02-20       Impact factor: 2.405

Review 8.  Prenatal exposures and infant brain: Review of magnetic resonance imaging studies and a population description analysis.

Authors:  Elmo P Pulli; Venla Kumpulainen; Jussi H Kasurinen; Riikka Korja; Harri Merisaari; Linnea Karlsson; Riitta Parkkola; Jani Saunavaara; Tuire Lähdesmäki; Noora M Scheinin; Hasse Karlsson; Jetro J Tuulari
Journal:  Hum Brain Mapp       Date:  2018-11-19       Impact factor: 5.038

9.  Third trimester-equivalent ethanol exposure increases anxiety-like behavior and glutamatergic transmission in the basolateral amygdala.

Authors:  Brian C Baculis; Marvin R Diaz; C Fernando Valenzuela
Journal:  Pharmacol Biochem Behav       Date:  2015-08-15       Impact factor: 3.533

10.  Alcohol exposure in utero is associated with decreased gray matter volume in neonates.

Authors:  Kirsten A Donald; J P Fouche; Annerine Roos; Nastassja Koen; Fleur M Howells; Edward P Riley; Roger P Woods; Heather J Zar; Katherine L Narr; Dan J Stein
Journal:  Metab Brain Dis       Date:  2015-11-29       Impact factor: 3.584

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.