Spoken word processing in Rett syndrome: Evidence from event-related potentials

被引:21
作者
Key, Alexandra P. [1 ,2 ,3 ]
Jones, Dorita [1 ]
Peters, Sarika [1 ,4 ]
机构
[1] Vanderbilt Kennedy Ctr Res Human Dev, Nashville, TN 37203 USA
[2] Vanderbilt Univ, Dept Hearing & Speech Sci, Med Ctr, Nashville, TN 37232 USA
[3] Vanderbilt Univ, Dept Psychiat & Behav Sci, Med Ctr, Nashville, TN 37232 USA
[4] Vanderbilt Univ, Med Ctr, Dept Pediat, Nashville, TN 37232 USA
关键词
Auditory; ERP; Rett syndrome; Speech; Word; CEREBRAL SPECIALIZATION; MECP2; DUPLICATION; CHILDREN; ERP; COMPREHENSION; AUTISM;
D O I
10.1016/j.ijdevneu.2019.01.001
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
This study examined the feasibility of using auditory event-related potentials to evaluate spoken word processing during passive listening in girls with Rett syndrome (n = 11) and typical peers (n = 33), age 4-12 years. The typical group demonstrated the expected pattern of more negative amplitudes within 200-500 ms in response to words than nonwords at left temporal sites. In participants with Rett syndrome, word-nonword differentiation was observed at the right temporal sites. More negative left hemisphere amplitudes in response to words were associated (at trend level) with better receptive language skills and more adaptive behavior. The results indicate that girls with Rett syndrome differentiate known words from novel nonwords, but may do so using potentially atypical neural processes. Brain-behavior correlations support validity of the proposed neural markers of word processing, making passive listening paradigms a promising approach for assessing speech and language processing in participants with limited spoken language skills.
引用
收藏
页码:26 / 31
页数:6
相关论文
共 30 条
[1]  
Aman MG., 1986, ABERRANT BEHAV CHECK
[2]   Anxiety-like behavior in Rett syndrome: characteristics and assessment by anxiety scales [J].
Barnes, Katherine V. ;
Coughlin, Francesca R. ;
O'Leary, Heather M. ;
Bruck, Natalie ;
Bazin, Grace A. ;
Beinecke, Emily B. ;
Walco, Alexandra C. ;
Cantwell, Nicole G. ;
Kaufmann, Walter E. .
JOURNAL OF NEURODEVELOPMENTAL DISORDERS, 2015, 7
[3]   Cognitive deficits in Rett syndrome: What we know and what we need to know to treat them [J].
Berger-Sweeney, Joanne .
NEUROBIOLOGY OF LEARNING AND MEMORY, 2011, 96 (04) :637-646
[4]   MeCP2: only 100% will do [J].
Chao, Hsiao-Tuan ;
Zoghbi, Huda Y. .
NATURE NEUROSCIENCE, 2012, 15 (02) :176-177
[5]   Mild overexpression of MeCP2 causes a progressive neurological disorder in mice [J].
Collins, AL ;
Levenson, JM ;
Vilaythong, AP ;
Richman, R ;
Armstrong, DL ;
Noebels, JL ;
Sweatt, JD ;
Zoghbi, HY .
HUMAN MOLECULAR GENETICS, 2004, 13 (21) :2679-2689
[6]   Assessing the developmental level in Rett syndrome: an alternative approach? [J].
Demeter, K .
EUROPEAN CHILD & ADOLESCENT PSYCHIATRY, 2000, 9 (03) :227-233
[7]  
Dunn D.M., 2007, Peabody Picture Vocabulary Test, Fourth Edition, manual, VFourth
[8]   Automatic cortical representation of auditory pitch changes in Rett syndrome [J].
Foxe, John J. ;
Burke, Kelly M. ;
Andrade, Gizely N. ;
Djukic, Aleksandra ;
Frey, Hans-Peter ;
Molholm, Sophie .
JOURNAL OF NEURODEVELOPMENTAL DISORDERS, 2016, 8
[9]   The Role of MeCP2 in Brain Development and Neurodevelopmental Disorders [J].
Gonzales, Michael L. ;
LaSalle, Janine M. .
CURRENT PSYCHIATRY REPORTS, 2010, 12 (02) :127-134
[10]   A PROGRESSIVE SYNDROME OF AUTISM, DEMENTIA, ATAXIA, AND LOSS OF PURPOSEFUL HAND USE IN GIRLS - RETTS SYNDROME - REPORT OF 35 CASES [J].
HAGBERG, B ;
AICARDI, J ;
DIAS, K ;
RAMOS, O .
ANNALS OF NEUROLOGY, 1983, 14 (04) :471-479