Specific effect of the fragile-X mental retardation-1 gene (FMR1) on white matter microstructure

被引:15
作者
Green, Tamar [1 ,2 ]
Barnea-Goraly, Naama [1 ]
Raman, Mira [1 ]
Hall, Scott S. [1 ]
Lightbody, Amy A. [1 ]
Bruno, Jennifer L. [1 ]
Quintin, Eve-Marie [1 ]
Reiss, Allan L. [3 ,4 ]
机构
[1] Stanford Univ, Sch Med, Ctr Interdisciplinary Brain Sci Res, Stanford, CA 94305 USA
[2] Tel Aviv Univ, Sackler Fac Med, IL-69978 Tel Aviv, Israel
[3] Stanford Univ, Sch Med, Ctr Interdisciplinary Brain Sci Res, Dept Psychiat & Behav Sci, Stanford, CA 94305 USA
[4] Stanford Univ, Sch Med, Dept Radiol, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
PROTEIN-SYNTHESIS; MOUSE MODEL; DIFFUSION; ABNORMALITIES; IDENTIFICATION; TRANSLATION; BEHAVIOR;
D O I
10.1192/bjp.bp.114.151654
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background Fragile-X syndrome (FXS) is a neurodevelopmental disorder associated with intellectual disability and neurobiological abnormalities including white matter microstructural differences. White matter differences have been found relative to neurotypical individuals. Aims To examine whether FXS white matter differences are related specifically to FXS or more generally to the presence of intellectual disability. Method We used voxel-based and tract-based analytic approaches to compare individuals with FXS (n = 40) with gender- and IQ-matched controls (n = 30). Results Individuals with FXS had increased fractional anisotropy and decreased radial diffusivity values compared with IQ-matched controls in the inferior longitudinal, inferior fronto-occipital and uncinate fasciculi. Conclusions The genetic variation associated with FXS affects white matter microstructure independently of overall IQ. White matter differences, found in FXS relative to IQ-matched controls, are distinct from reported differences relative to neurotypical controls. This underscores the need to consider cognitive ability differences when investigating white matter microstructure in neurodevelopmental disorders. Copyright and usage (C) The Royal College of Psychiatrists, all rights reserved.
引用
收藏
页码:143 / 148
页数:6
相关论文
共 39 条
[1]   White matter tract alterations in fragile X syndrome: Preliminary evidence from diffusion tensor imaging [J].
Barnea-Goraly, N ;
Eliez, S ;
Hedeus, M ;
Menon, V ;
White, CD ;
Moseley, M ;
Reiss, AL .
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2003, 118B (01) :81-88
[2]   Characterization and propagation of uncertainty in diffusion-weighted MR imaging [J].
Behrens, TEJ ;
Woolrich, MW ;
Jenkinson, M ;
Johansen-Berg, H ;
Nunes, RG ;
Clare, S ;
Matthews, PM ;
Brady, JM ;
Smith, SM .
MAGNETIC RESONANCE IN MEDICINE, 2003, 50 (05) :1077-1088
[3]   Outcome Measures for Clinical Trials in Fragile X Syndrome [J].
Berry-Kravis, Elizabeth ;
Hessl, David ;
Abbeduto, Leonard ;
Reiss, Allan L. ;
Beckel-Mitchener, Andrea ;
Urv, Tiina K. .
JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS, 2013, 34 (07) :508-522
[4]   Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome [J].
Brown, V ;
Jin, P ;
Ceman, S ;
Darnell, JC ;
O'Donnell, WT ;
Tenenbaum, SA ;
Jin, XK ;
Feng, Y ;
Wilkinson, KD ;
Keene, JD ;
Darnell, RB ;
Warren, ST .
CELL, 2001, 107 (04) :477-487
[5]   Chemotropic responses of retinal growth cones mediated by rapid local protein synthesis and degradation [J].
Campbell, DS ;
Holt, CE .
NEURON, 2001, 32 (06) :1013-1026
[6]   FMR1 and the fragile X syndrome:: Human genome epidemiology review [J].
Crawford, DC ;
Acuña, JM ;
Sherman, SL .
GENETICS IN MEDICINE, 2001, 3 (05) :359-371
[7]   Automatically parcellating the human cerebral cortex [J].
Fischl, B ;
van der Kouwe, A ;
Destrieux, C ;
Halgren, E ;
Ségonne, F ;
Salat, DH ;
Busa, E ;
Seidman, LJ ;
Goldstein, J ;
Kennedy, D ;
Caviness, V ;
Makris, N ;
Rosen, B ;
Dale, AM .
CEREBRAL CORTEX, 2004, 14 (01) :11-22
[8]   Biological and environmental contributions to adaptive behavior in fragile X syndrome [J].
Glaser, B ;
Hessl, D ;
Dyer-Friedman, J ;
Johnston, C ;
Wisbeck, J ;
Taylor, A ;
Reiss, A .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2003, 117A (01) :21-29
[9]   Early white-matter abnormalities of the ventral frontostriatal pathway in fragile X syndrome [J].
Haas, Brian W. ;
Barnea-Goraly, Naama ;
Lightbody, Amy A. ;
Patnaik, Swetapadma S. ;
Hoeft, Fumiko ;
Hazlett, Heather ;
Piven, Joseph ;
Reiss, Allan L. .
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 2009, 51 (08) :593-599
[10]   Region-specific alterations in brain development in one- to three-year-old boys with fragile X syndrome [J].
Hoeft, Fumiko ;
Carter, John C. ;
Lightbody, Amy A. ;
Hazlett, Heather Cody ;
Piven, Joseph ;
Reiss, Allan L. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (20) :9335-9339