Literature DB >> 25603839

Hyperactive auditory processing in Williams syndrome: Evidence from auditory evoked potentials.

Omer Zarchi1,2,3, Chen Avni3, Josef Attias2,4, Amos Frisch3,5, Miri Carmel3,5, Elena Michaelovsky5, Tamar Green3,6, Abraham Weizman3,5,7, Doron Gothelf1,3.   

Abstract

The neurophysiologic aberrations underlying the auditory hypersensitivity in Williams syndrome (WS) are not well defined. The P1-N1-P2 obligatory complex and mismatch negativity (MMN) response were investigated in 18 participants with WS, and the results were compared with those of 18 age- and gender-matched typically developing (TD) controls. Results revealed significantly higher amplitudes of both the P1-N1-P2 obligatory complex and the MMN response in the WS participants than in the TD controls. The P1-N1-P2 complex showed an age-dependent reduction in the TD but not in the WS participants. Moreover, high P1-N1-P2 complex was associated with low verbal comprehension scores in WS. This investigation demonstrates that central auditory processing is hyperactive in WS. The increase in auditory brain responses of both the obligatory complex and MMN response suggests aberrant processes of auditory encoding and discrimination in WS. Results also imply that auditory processing may be subjected to a delayed or diverse maturation and may affect the development of high cognitive functioning in WS.
© 2015 Society for Psychophysiological Research.

Entities:  

Keywords:  Auditory processing; Evoked response potentials (ERP); Hyperacusis; Williams syndrome

Mesh:

Year:  2015        PMID: 25603839     DOI: 10.1111/psyp.12407

Source DB:  PubMed          Journal:  Psychophysiology        ISSN: 0048-5772            Impact factor:   4.016


  5 in total

1.  Innate frequency-discrimination hyperacuity in Williams-Beuren syndrome mice.

Authors:  Christopher M Davenport; Brett J W Teubner; Seung Baek Han; Mary H Patton; Tae-Yeon Eom; Dusan Garic; Benjamin J Lansdell; Abbas Shirinifard; Ti-Cheng Chang; Jonathon Klein; Shondra M Pruett-Miller; Jay A Blundon; Stanislav S Zakharenko
Journal:  Cell       Date:  2022-09-23       Impact factor: 66.850

2.  Comparing the broad socio-cognitive profile of youth with Williams syndrome and 22q11.2 deletion syndrome.

Authors:  O Weisman; R Feldman; M Burg-Malki; M Keren; R Geva; G Diesendruck; D Gothelf
Journal:  J Intellect Disabil Res       Date:  2017-10-08

3.  Noise-Induced loudness recruitment and hyperacusis: Insufficient central gain in auditory cortex and amygdala.

Authors:  Kelly Radziwon; Benjamin D Auerbach; Dalian Ding; Xiaopeng Liu; Guang-Di Chen; Richard Salvi
Journal:  Neuroscience       Date:  2019-10-26       Impact factor: 3.590

4.  Neurophysiological Correlates of Dynamic Beat Tracking in Individuals With Williams Syndrome.

Authors:  Anna Kasdan; Reyna L Gordon; Miriam D Lense
Journal:  Biol Psychiatry Cogn Neurosci Neuroimaging       Date:  2020-10-22

5.  Effects of Age and Type of Stimulus on the Cortical Auditory Evoked Potential in Healthy Malaysian Children.

Authors:  Siti Zamratol-Mai Sarah Mukari; Cila Umat; Soon Chien Chan; Akmaliza Ali; Nashrah Maamor; Mohd Normani Zakaria
Journal:  J Audiol Otol       Date:  2020-01-02
  5 in total

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