Literature DB >> 12705812

Augmentation of auditory N1 in children with fragile X syndrome.

Maija Castrén1, Ari Pääkkönen, Ina M Tarkka, Markku Ryynänen, Juhani Partanen.   

Abstract

We compared the N1 responses of the auditory event-related brain potentials (ERPs) in school-aged children with fragile X syndrome to age-matched controls in order to assess auditory processing. Event-related potentials to non-attended standard and deviant tone stimuli were recorded with EEG electrodes and here the standard tones were analysed. The amplitude of the N1 component to standard tones was significantly larger in children with fragile X syndrome than in control children. In addition, the global field power maximum of ERP corresponding to the N2 component was significantly (p<0.05) larger in fragile X children than in controls. The N2 scalp distribution in children with fragile X syndrome appeared more frontal than that in controls. Furthermore, the fragile X children exhibited no habituation of N1 and an absence of N2 sensitization for repeated tones. Increased responsiveness observed in the N1 evoked potential together with abnormal habituation of auditory responses in childhood may indicate increased sensory sensitivity for auditory stimuli in fragile X syndrome. The data, though very limited, suggest that stimulus processing in the auditory afferent pathways and/or in the corresponding cortical receiving areas is abnormal in children with fragile X syndrome.

Entities:  

Mesh:

Year:  2003        PMID: 12705812     DOI: 10.1023/a:1022606200636

Source DB:  PubMed          Journal:  Brain Topogr        ISSN: 0896-0267            Impact factor:   3.020


  55 in total

1.  Modulators of Kv3 Potassium Channels Rescue the Auditory Function of Fragile X Mice.

Authors:  Lynda El-Hassar; Lei Song; Winston J T Tan; Charles H Large; Giuseppe Alvaro; Joseph Santos-Sacchi; Leonard K Kaczmarek
Journal:  J Neurosci       Date:  2019-04-01       Impact factor: 6.167

2.  Deletion of Fmr1 from Forebrain Excitatory Neurons Triggers Abnormal Cellular, EEG, and Behavioral Phenotypes in the Auditory Cortex of a Mouse Model of Fragile X Syndrome.

Authors:  Jonathan W Lovelace; Maham Rais; Arnold R Palacios; Xinghao S Shuai; Steven Bishay; Otilia Popa; Patricia S Pirbhoy; Devin K Binder; David L Nelson; Iryna M Ethell; Khaleel A Razak
Journal:  Cereb Cortex       Date:  2020-03-14       Impact factor: 5.357

Review 3.  Altered Neuronal and Circuit Excitability in Fragile X Syndrome.

Authors:  Anis Contractor; Vitaly A Klyachko; Carlos Portera-Cailliau
Journal:  Neuron       Date:  2015-08-19       Impact factor: 17.173

Review 4.  Sensory processing in autism spectrum disorders and Fragile X syndrome-From the clinic to animal models.

Authors:  D Sinclair; B Oranje; K A Razak; S J Siegel; S Schmid
Journal:  Neurosci Biobehav Rev       Date:  2016-05-24       Impact factor: 8.989

5.  MeCP2+/- mouse model of RTT reproduces auditory phenotypes associated with Rett syndrome and replicate select EEG endophenotypes of autism spectrum disorder.

Authors:  Wenlin Liao; Michael J Gandal; Richard S Ehrlichman; Steven J Siegel; Greg C Carlson
Journal:  Neurobiol Dis       Date:  2012-01-09       Impact factor: 5.996

Review 6.  Disrupted circuits in mouse models of autism spectrum disorder and intellectual disability.

Authors:  Carla Em Golden; Joseph D Buxbaum; Silvia De Rubeis
Journal:  Curr Opin Neurobiol       Date:  2017-12-07       Impact factor: 6.627

7.  Potential Involvement of Impaired BKCa Channel Function in Sensory Defensiveness and Some Behavioral Disturbances Induced by Unfamiliar Environment in a Mouse Model of Fragile X Syndrome.

Authors:  Maria Isabel Carreno-Munoz; Fabienne Martins; Maria Carmen Medrano; Elisabetta Aloisi; Susanna Pietropaolo; Corentin Dechaud; Enejda Subashi; Guillaume Bony; Melanie Ginger; Abdelmalik Moujahid; Andreas Frick; Xavier Leinekugel
Journal:  Neuropsychopharmacology       Date:  2017-07-19       Impact factor: 7.853

Review 8.  Fragile X: a family of disorders.

Authors:  Weerasak Chonchaiya; Andrea Schneider; Randi J Hagerman
Journal:  Adv Pediatr       Date:  2009

9.  Imbalance of neocortical excitation and inhibition and altered UP states reflect network hyperexcitability in the mouse model of fragile X syndrome.

Authors:  Jay R Gibson; Aundrea F Bartley; Seth A Hays; Kimberly M Huber
Journal:  J Neurophysiol       Date:  2008-09-10       Impact factor: 2.714

Review 10.  Review of targeted treatments in fragile X syndrome.

Authors:  Andrew Ligsay; Randi J Hagerman
Journal:  Intractable Rare Dis Res       Date:  2016-08
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.