Auditory evoked response delays in children with 47,XYY syndrome.


Journal

Neuroreport
ISSN: 1473-558X
Titre abrégé: Neuroreport
Pays: England
ID NLM: 9100935

Informations de publication

Date de publication:
01 05 2019
Historique:
pubmed: 22 3 2019
medline: 4 12 2019
entrez: 22 3 2019
Statut: ppublish

Résumé

47,XYY syndrome (XYY) is a male sex chromosome disorder where individuals have an X chromosome and two copies of the Y chromosome. XYY is associated with a physical phenotype and carries increased risk of neurodevelopmental disorders such as autism spectrum disorder (ASD). Latencies of auditory evoked responses measured by magnetoencephalography have shown atypical prolongations in several neuropsychiatric and genetic disorders; specifically, delayed auditory responses have been observed in ASD. In this study, we investigated the associations of genotype and clinical phenotype with auditory processing. Whole cortex magnetoencephalography recorded during a passive auditory paradigm (500 Hz tones) was used to assess the auditory evoked response in three groups of male children: idiopathic ASD, typically developing, and XYY boys. Response waveforms were computed for left and right auditory cortex and latencies of the ∼50 ms (M50) and ∼100 ms (M100) components were determined. M50 latencies were significantly delayed compared with typically developing controls in children with ASD in the right hemisphere only, and in children with XYY in the left hemisphere only, irrespective of whether they met diagnostic criteria for ASD. Findings on the later M100 component trended in the same directions but did not attain significance, due to increased variance. Replicating previous findings, decreased M50 and M100 latencies with age were observed bilaterally. Overall, while XYY shares an electrophysiological phenotype (delayed evoked response latency) with idiopathic ASD, the hemispheric differences warrant further investigation.

Identifiants

pubmed: 30896674
doi: 10.1097/WNR.0000000000001233
pmc: PMC6544154
mid: NIHMS1523499
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

504-509

Subventions

Organisme : NIMH NIH HHS
ID : K01 MH108762
Pays : United States
Organisme : NIDCD NIH HHS
ID : R01 DC008871
Pays : United States
Organisme : NIMH NIH HHS
ID : R21 MH109158
Pays : United States
Organisme : NICHD NIH HHS
ID : U54 HD086984
Pays : United States

Références

J Autism Dev Disord. 2003 Aug;33(4):427-33
pubmed: 12959421
Neuroimage. 2003 Oct;20(2):995-1005
pubmed: 14568469
Cereb Cortex. 2004 Feb;14(2):156-64
pubmed: 14704212
Neuroreport. 2004 Aug 26;15(12):1867-70
pubmed: 15305126
J Clin Endocrinol Metab. 2006 Apr;91(4):1423-7
pubmed: 16403821
Birth Defects Orig Artic Ser. 1990;26(4):59-115
pubmed: 1708685
Brain Topogr. 1991 Winter;4(2):143-50
pubmed: 1793688
Am J Med Genet B Neuropsychiatr Genet. 2009 Jan 5;150B(1):74-85
pubmed: 18454450
Hear Res. 2009 Nov;257(1-2):41-52
pubmed: 19647788
Neuroreport. 2009 Dec 9;20(18):1586-91
pubmed: 19898261
Dev Disabil Res Rev. 2009;15(4):269
pubmed: 20014365
Autism Res. 2010 Feb;3(1):8-18
pubmed: 20063319
Orphanet J Rare Dis. 2010 May 29;5:15
pubmed: 20509956
Arch Dis Child. 2011 Oct;96(10):954-9
pubmed: 20656736
Acta Paediatr. 2011 Jun;100(6):903-7
pubmed: 21418292
Pediatrics. 2012 Apr;129(4):769-78
pubmed: 22412026
Schizophr Res. 2012 Sep;140(1-3):250-7
pubmed: 22766129
J Pediatr. 2013 Oct;163(4):1085-94
pubmed: 23810129
Brain Res. 2013 Nov 6;1537:79-85
pubmed: 24055954
Schizophr Res. 2014 Dec;160(1-3):201-7
pubmed: 25468188
Genes Brain Behav. 2015 Feb;14(2):137-44
pubmed: 25558953
Cereb Cortex. 2016 May;26(5):1957-64
pubmed: 25678630
Mol Autism. 2015 Dec 30;6:69
pubmed: 26719787
J Dev Behav Pediatr. 2017 Apr;38(3):197-207
pubmed: 28333849
Psychophysiology. 2017 Aug;54(8):1110-1127
pubmed: 28421620
Front Hum Neurosci. 2017 May 26;11:259
pubmed: 28603492
Dev Neurosci. 2017;39(5):430-441
pubmed: 28772264
MMWR Surveill Summ. 2018 Apr 27;67(6):1-23
pubmed: 29701730
Birth Defects Orig Artic Ser. 1986;22(3):293-306
pubmed: 3814782

Auteurs

Luke Bloy (L)

Department of Radiology, Lurie Family Foundations MEG Imaging Center.

Matthew Ku (M)

Department of Radiology, Lurie Family Foundations MEG Imaging Center.

J Christopher Edgar (JC)

Department of Radiology, Lurie Family Foundations MEG Imaging Center.

Judith S Miller (JS)

Center for Autism Research, Children's Hospital of Philadelphia.

Lisa Blaskey (L)

Department of Radiology, Lurie Family Foundations MEG Imaging Center.
Center for Autism Research, Children's Hospital of Philadelphia.

Judith Ross (J)

Department of Pediatrics, Thomas Jefferson University, Philadelphia, Pennsylvania.
Department of Pediatrics, Nemours DuPont Hospital for Children, Wilmington, Delaware, USA.

Timothy P L Roberts (TPL)

Department of Radiology, Lurie Family Foundations MEG Imaging Center.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH