Suppr超能文献

普拉德-威利综合征不同基因亚型患儿对面孔的偶发记忆。

Incidental memory for faces in children with different genetic subtypes of Prader-Willi syndrome.

作者信息

Key Alexandra P, Dykens Elisabeth M

机构信息

Vanderbilt Kennedy Center for Research on Human Development.

Department of Hearing and Speech Sciences, Vanderbilt University Medical Center.

出版信息

Soc Cogn Affect Neurosci. 2017 Jun 1;12(6):918-927. doi: 10.1093/scan/nsx013.

Abstract

The present study examined the effects of genetic subtype on social memory in children (7-16 years) with Prader-Willi syndrome (PWS). Visual event-related potentials (ERPs) during a passive viewing task were used to compare incidental memory traces for repeated vs single presentations of previously unfamiliar social (faces) and nonsocial (houses) images in 15 children with the deletion subtype and 13 children with maternal uniparental disomy (mUPD). While all participants perceived faces as different from houses (N170 responses), repeated faces elicited more positive ERP amplitudes ('old/new' effect, 250-500ms) only in children with the deletion subtype. Conversely, the mUPD group demonstrated reduced amplitudes suggestive of habituation to the repeated faces. ERP responses to repeated vs single house images did not differ in either group. The results suggest that faces hold different motivational value for individuals with the deletion vs mUPD subtype of PWS and could contribute to the explanation of subtype differences in the psychiatric symptoms, including autism symptomatology.

摘要

本研究调查了基因亚型对普拉德-威利综合征(PWS)患儿(7至16岁)社会记忆的影响。在一项被动观看任务中,利用视觉事件相关电位(ERP),比较了15名缺失亚型患儿和13名母源单亲二倍体(mUPD)患儿对先前不熟悉的社会(面孔)和非社会(房屋)图像的重复呈现与单次呈现的 incidental 记忆痕迹。虽然所有参与者都将面孔视为与房屋不同(N170反应),但只有缺失亚型的患儿,重复面孔会引发更正向的ERP波幅(“旧/新”效应,250 - 500毫秒)。相反,mUPD组的波幅降低,表明对重复面孔产生了习惯化。两组中,对重复房屋图像与单次房屋图像的ERP反应均无差异。结果表明,面孔对PWS缺失亚型与mUPD亚型个体具有不同的动机价值,这可能有助于解释包括自闭症症状在内的精神症状的亚型差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfd0/5472135/3555667d6fd2/nsx013f1.jpg

相似文献

1
Incidental memory for faces in children with different genetic subtypes of Prader-Willi syndrome.
Soc Cogn Affect Neurosci. 2017 Jun 1;12(6):918-927. doi: 10.1093/scan/nsx013.
2
Differences in behavioural phenotype between parental deletion and maternal uniparental disomy in Prader-Willi syndrome: an ERP study.
Clin Neurophysiol. 2005 Jun;116(6):1464-70. doi: 10.1016/j.clinph.2005.02.019. Epub 2005 Apr 26.
3
Social and emotional processing in Prader-Willi syndrome: genetic subtype differences.
J Neurodev Disord. 2013 Mar 27;5(1):7. doi: 10.1186/1866-1955-5-7.
4
Face and gaze processing in Prader-Willi syndrome.
J Neuropsychol. 2008 Mar;2(1):65-77. doi: 10.1348/174866407x243305.
6
'Hungry Eyes': visual processing of food images in adults with Prader-Willi syndrome.
J Intellect Disabil Res. 2008 Jun;52(Pt 6):536-46. doi: 10.1111/j.1365-2788.2008.01062.x. Epub 2008 Apr 15.
7
Expressive and receptive language in Prader-Willi syndrome: report on genetic subtype differences.
J Commun Disord. 2013 Mar-Apr;46(2):193-201. doi: 10.1016/j.jcomdis.2012.12.001. Epub 2012 Dec 21.
8
Prader-Willi syndrome: intellectual abilities and behavioural features by genetic subtype.
J Child Psychol Psychiatry. 2005 Oct;46(10):1089-96. doi: 10.1111/j.1469-7610.2005.01520.x.
9
Early Social Cognitive Ability in Preschoolers with Prader-Willi Syndrome and Autism Spectrum Disorder.
J Autism Dev Disord. 2019 Nov;49(11):4441-4454. doi: 10.1007/s10803-019-04152-4.
10
Genetic subtype differences in neural circuitry of food motivation in Prader-Willi syndrome.
Int J Obes (Lond). 2009 Feb;33(2):273-83. doi: 10.1038/ijo.2008.255. Epub 2008 Dec 2.

引用本文的文献

1
Altered Behavior and Neuronal Activity with Paternal Deletion.
Genes (Basel). 2025 Jul 24;16(8):863. doi: 10.3390/genes16080863.
3
Peers, play, and performance to build social salience in autistic youth: A multisite randomized clinical trial.
J Consult Clin Psychol. 2023 Jul;91(7):411-425. doi: 10.1037/ccp0000821. Epub 2023 May 18.
5
Face individual identity recognition: a potential endophenotype in autism.
Mol Autism. 2020 Oct 21;11(1):81. doi: 10.1186/s13229-020-00371-0.
6
Face processing and exploration of social signals in Prader-Willi syndrome: a genetic signature.
Orphanet J Rare Dis. 2019 Nov 15;14(1):262. doi: 10.1186/s13023-019-1221-3.
7
The Unfulfilled Promise of the N170 as a Social Biomarker.
Biol Psychiatry Cogn Neurosci Neuroimaging. 2020 Mar;5(3):342-353. doi: 10.1016/j.bpsc.2019.08.011. Epub 2019 Sep 13.
8
Treatment Effects in Social Cognition and Behavior following a Theater-based Intervention for Youth with Autism.
Dev Neuropsychol. 2019 Oct;44(7):481-494. doi: 10.1080/87565641.2019.1676244. Epub 2019 Oct 7.

本文引用的文献

1
Face repetition detection and social interest: An ERP study in adults with and without Williams syndrome.
Soc Neurosci. 2016 Dec;11(6):652-64. doi: 10.1080/17470919.2015.1130743. Epub 2016 Jan 10.
3
Autism spectrum disorder in Prader-Willi syndrome: A systematic review.
Am J Med Genet A. 2015 Dec;167A(12):2936-44. doi: 10.1002/ajmg.a.37286. Epub 2015 Aug 29.
4
Cognitive and behavioural aspects of Prader-Willi syndrome.
Curr Opin Psychiatry. 2015 Mar;28(2):102-6. doi: 10.1097/YCO.0000000000000135.
6
Event-related potential index of age-related differences in memory processes in adults with Down syndrome.
Neurobiol Aging. 2014 Jan;35(1):247-53. doi: 10.1016/j.neurobiolaging.2013.07.024. Epub 2013 Aug 29.
7
Social and emotional processing in Prader-Willi syndrome: genetic subtype differences.
J Neurodev Disord. 2013 Mar 27;5(1):7. doi: 10.1186/1866-1955-5-7.
8
The suppression of repetition enhancement: a review of fMRI studies.
Neuropsychologia. 2013 Jan;51(1):59-66. doi: 10.1016/j.neuropsychologia.2012.11.006. Epub 2012 Nov 14.
9
Recognition of emotions in autism: a formal meta-analysis.
J Autism Dev Disord. 2013 Jul;43(7):1517-26. doi: 10.1007/s10803-012-1695-5.
10
Implementation of false discovery rate for exploring novel paradigms and trait dimensions with ERPs.
Dev Neuropsychol. 2012;37(6):559-77. doi: 10.1080/87565641.2012.694513.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验