Gray matter abnormalities in autism spectrum disorder revealed by T2 relaxation

被引:28
作者
Petropoulos, H.
Friedman, S. D.
Shaw, D. W. W.
Artru, A. A.
Dawson, G.
Dager, S. R.
机构
[1] Univ Washington, Sch Med, Dept Radiol, Neuroimaging Res Grp, Seattle, WA 98105 USA
[2] Univ Washington, Sch Med, Dept Anesthesiol, Seattle, WA 98105 USA
[3] Univ Washington, Sch Med, Dept Psychol, Seattle, WA 98105 USA
[4] Univ Washington, Sch Med, Dept Psychiat, Seattle, WA 98105 USA
[5] Univ Washington, Sch Med, Dept Bioengn, Seattle, WA 98105 USA
关键词
WHITE-MATTER; BRAIN-DEVELOPMENT; YOUNG-CHILDREN; HEAD CIRCUMFERENCE; MR; AGE; MYELINATION; MATURATION; VOLUME; TIMES;
D O I
10.1212/01.wnl.0000229923.08213.1e
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To perform quantitative T2 relaxation measurements to evaluate cerebral water content in children with autism. Methods: Sixty 2- to 4-year-old children with autism spectrum disorder (ASD), 16 age-matched children with idiopathic developmental delay (DD), and 10 children with typical development (TD) were scanned on a 1.5 T GE MRI scanner to obtain dual-echo fast spin echo images (2.5 mm thick, 0-mm gap). Images were segmented into gray and white matter and used to mask regions of interest for calculating T2 for each tissue type. Analysis of variance, covarying for age and sex, was used to compare T2 between groups, and correlations were used to compare T2 to IQ measures. Results: Children with ASD had prolonged cortical gray matter T2, but white matter T2 was not significantly different, compared with the children with TD. T2 was prolonged in cortical gray matter and white matter in children with DD compared with children with ASD or TD. Significant interactions between T2 measures and IQ were not observed. Conclusions: Prolonged gray and white matter T2 in the children with developmental delay likely represents a delay in neuronal development and maturation. Prolonged T2 in gray matter, but not white matter, observed in children with autism spectrum disorder may signify abnormal developmental processes specific to autism.
引用
收藏
页码:632 / 636
页数:5
相关论文
共 47 条
[1]   Propofol Sedation for Longitudinal Pediatric Neuroimaging Research [J].
Amundsen, Laurie B. ;
Artru, Alan A. ;
Dager, Stephen R. ;
Shaw, Dennis W. W. ;
Friedman, Seth ;
Sparks, Bobbi ;
Dawson, Geraldine .
JOURNAL OF NEUROSURGICAL ANESTHESIOLOGY, 2005, 17 (04) :180-192
[2]   Brain T2 relaxation times correlate with regional cerebral blood volume [J].
Anderson, CM ;
Kaufman, MJ ;
Lowen, SB ;
Rohan, M ;
Renshaw, PF ;
Teicher, MH .
MAGNETIC RESONANCE MATERIALS IN PHYSICS BIOLOGY AND MEDICINE, 2005, 18 (01) :3-6
[3]   Effects of age on brain volume and head circumference in autism [J].
Aylward, EH ;
Minshew, NJ ;
Field, K ;
Sparks, BF ;
Singh, N .
NEUROLOGY, 2002, 59 (02) :175-183
[4]   Comparative MR imaging study of brain maturation in kittens with T1, T2, and the trace of the diffusion tensor [J].
Baratti, C ;
Barnett, AS ;
Pierpaoli, C .
RADIOLOGY, 1999, 210 (01) :133-142
[5]  
Barkovich AJ, 2000, AM J NEURORADIOL, V21, P1099
[6]   Cerebral lobes in autism: Early hyperplasia and abnormal age effects [J].
Carper, RA ;
Moses, P ;
Tigue, ZD ;
Courchesne, E .
NEUROIMAGE, 2002, 16 (04) :1038-1051
[7]   Minicolumnar pathology in autism [J].
Casanova, MF ;
Buxhoeveden, DP ;
Switala, AE ;
Roy, E .
NEUROLOGY, 2002, 58 (03) :428-432
[8]   Serotonin in autism and pediatric epilepsies [J].
Chugani, DC .
MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS, 2004, 10 (02) :112-116
[9]   Brain overgrowth in autism during a critical time in development: implications for frontal pyramidal neuron and interneuron development and connectivity [J].
Courchesne, E ;
Pierce, K .
INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, 2005, 23 (2-3) :153-170
[10]   Brain development in autism: Early overgrowth followed by premature arrest of growth [J].
Courchesne, E .
MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS, 2004, 10 (02) :106-111