• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Neuroanatomical abnormalities in fragile X syndrome during the adolescent and young adult years.脆性 X 综合征青少年及青年期的神经解剖学异常。
J Psychiatr Res. 2018 Dec;107:138-144. doi: 10.1016/j.jpsychires.2018.10.014. Epub 2018 Oct 25.
2
Region-specific alterations in brain development in one- to three-year-old boys with fragile X syndrome.脆性 X 综合征患儿 1 至 3 岁时大脑发育的区域特异性改变。
Proc Natl Acad Sci U S A. 2010 May 18;107(20):9335-9. doi: 10.1073/pnas.1002762107. Epub 2010 May 3.
3
Brain gray and white matter abnormalities in preterm-born adolescents: A meta-analysis of voxel-based morphometry studies.早产儿青少年大脑灰质和白质异常:基于体素的形态计量学研究的荟萃分析。
PLoS One. 2018 Oct 10;13(10):e0203498. doi: 10.1371/journal.pone.0203498. eCollection 2018.
4
Specific effect of the fragile-X mental retardation-1 gene (FMR1) on white matter microstructure.脆性X智力低下1基因(FMR1)对白质微观结构的特定影响。
Br J Psychiatry. 2015 Aug;207(2):143-8. doi: 10.1192/bjp.bp.114.151654. Epub 2015 Mar 19.
5
Decreased gray matter volume and increased white matter volume in patients with neovascular age-related macular degeneration: a voxel-based morphometry study.年龄相关性黄斑变性新生血管患者的灰质体积减少和白质体积增加:基于体素的形态计量学研究。
Aging (Albany NY). 2021 Oct 6;13(19):23182-23192. doi: 10.18632/aging.203610.
6
Topological methods reveal high and low functioning neuro-phenotypes within fragile X syndrome.拓扑学方法揭示了脆性X综合征中高功能和低功能神经表型。
Hum Brain Mapp. 2014 Sep;35(9):4904-15. doi: 10.1002/hbm.22521. Epub 2014 Apr 15.
7
Neuroanatomical Profile of Young Females with Fragile X Syndrome: A Voxel-Based Morphometry Analysis.脆性 X 综合征年轻女性的神经解剖学特征:基于体素的形态计量学分析。
Cereb Cortex. 2022 May 31;32(11):2310-2320. doi: 10.1093/cercor/bhab319.
8
White and Gray Matter Volume Changes and Correlation with Visual Evoked Potential in Patients with Optic Neuritis: A Voxel-Based Morphometry Study.视神经炎患者白质和灰质体积变化及其与视觉诱发电位的相关性:基于体素的形态学研究
Med Sci Monit. 2016 Apr 5;22:1115-23. doi: 10.12659/msm.897837.
9
Development of White Matter Circuitry in Infants With Fragile X Syndrome.脆性 X 综合征婴儿的脑白质回路发育。
JAMA Psychiatry. 2018 May 1;75(5):505-513. doi: 10.1001/jamapsychiatry.2018.0180.
10
Neuroanatomical differences in toddler boys with fragile x syndrome and idiopathic autism.患有脆性X综合征和特发性自闭症的学步期男孩的神经解剖学差异。
Arch Gen Psychiatry. 2011 Mar;68(3):295-305. doi: 10.1001/archgenpsychiatry.2010.153. Epub 2010 Nov 1.

引用本文的文献

1
Systematic Review: Fragile X Syndrome Across the Lifespan with a Focus on Genetics, Neurodevelopmental, Behavioral and Psychiatric Associations.系统评价:全生命周期的脆性X综合征,重点关注遗传学、神经发育、行为及精神方面的关联
Genes (Basel). 2025 Jan 25;16(2):149. doi: 10.3390/genes16020149.
2
Fragile X cortex is characterized by decreased parvalbumin-expressing interneurons.脆性 X 皮层的特征是表达 parvalbumin 的中间神经元减少。
Cereb Cortex. 2024 Mar 1;34(3). doi: 10.1093/cercor/bhae103.
3
Glial dysregulation in the human brain in fragile X-associated tremor/ataxia syndrome.脆性 X 相关震颤/共济失调综合征患者大脑中的神经胶质功能失调。
Proc Natl Acad Sci U S A. 2023 Jun 6;120(23):e2300052120. doi: 10.1073/pnas.2300052120. Epub 2023 May 30.
4
Primary Cilia Dysfunction in Neurodevelopmental Disorders beyond Ciliopathies.超越纤毛病的神经发育障碍中的原发性纤毛功能障碍
J Dev Biol. 2022 Dec 13;10(4):54. doi: 10.3390/jdb10040054.
5
Epilepsy Characteristics in Neurodevelopmental Disorders: Research from Patient Cohorts and Animal Models Focusing on Autism Spectrum Disorder.神经发育障碍中的癫痫特征:以自闭症谱系障碍为重点的患者队列和动物模型研究。
Int J Mol Sci. 2022 Sep 16;23(18):10807. doi: 10.3390/ijms231810807.
6
Neuroanatomical Profile of Young Females with Fragile X Syndrome: A Voxel-Based Morphometry Analysis.脆性 X 综合征年轻女性的神经解剖学特征:基于体素的形态计量学分析。
Cereb Cortex. 2022 May 31;32(11):2310-2320. doi: 10.1093/cercor/bhab319.
7
An "Omic" Overview of Fragile X Syndrome.脆性X综合征的“组学”概述
Biology (Basel). 2021 May 13;10(5):433. doi: 10.3390/biology10050433.
8
Altered dopaminergic pathways and therapeutic effects of intranasal dopamine in two distinct mouse models of autism.改变多巴胺能通路和鼻腔内给予多巴胺在两种不同自闭症小鼠模型中的治疗效果。
Mol Brain. 2020 Aug 10;13(1):111. doi: 10.1186/s13041-020-00649-7.
9
Graded Cerebellar Lobular Volume Deficits in Adolescents and Young Adults with Fetal Alcohol Spectrum Disorders (FASD).青少年和青年期酒精谱系障碍(FASD)患者小脑小叶体积的分级缺陷。
Cereb Cortex. 2020 Jul 30;30(9):4729-4746. doi: 10.1093/cercor/bhaa020.
10
Fragile X syndrome and associated disorders: Clinical aspects and pathology.脆性 X 综合征及相关疾病:临床特征与病理学
Neurobiol Dis. 2020 Mar;136:104740. doi: 10.1016/j.nbd.2020.104740. Epub 2020 Jan 10.

本文引用的文献

1
Longitudinal identification of clinically distinct neurophenotypes in young children with fragile X syndrome.脆性 X 综合征患儿神经表型的纵向鉴定。
Proc Natl Acad Sci U S A. 2017 Oct 3;114(40):10767-10772. doi: 10.1073/pnas.1620994114. Epub 2017 Sep 18.
2
A review of joint attention and social-cognitive brain systems in typical development and autism spectrum disorder.综述:典型发展和自闭症谱系障碍中的共同注意和社会认知大脑系统。
Eur J Neurosci. 2018 Mar;47(6):497-514. doi: 10.1111/ejn.13720. Epub 2017 Oct 25.
3
Two years changes in the development of caudate nucleus are involved in restricted repetitive behaviors in 2-5-year-old children with autism spectrum disorder.尾状核发育的两年变化与2至5岁自闭症谱系障碍儿童的受限重复行为有关。
Dev Cogn Neurosci. 2016 Jun;19:137-43. doi: 10.1016/j.dcn.2016.02.010. Epub 2016 Mar 11.
4
The cognitive developmental profile associated with fragile X syndrome: A longitudinal investigation of cognitive strengths and weaknesses through childhood and adolescence.与脆性X综合征相关的认知发展概况:一项贯穿童年和青春期对认知优势与劣势的纵向调查。
Dev Psychopathol. 2016 Nov;28(4pt2):1457-1469. doi: 10.1017/S0954579415001200. Epub 2015 Dec 9.
5
Fornix as an imaging marker for episodic memory deficits in healthy aging and in various neurological disorders.穹窿作为健康衰老和各种神经疾病中情景记忆缺陷的影像学标志物。
Front Aging Neurosci. 2015 Jan 14;6:343. doi: 10.3389/fnagi.2014.00343. eCollection 2014.
6
Metabotropic glutamate receptor 5 negative allosteric modulators: discovery of 2-chloro-4-[1-(4-fluorophenyl)-2,5-dimethyl-1H-imidazol-4-ylethynyl]pyridine (basimglurant, RO4917523), a promising novel medicine for psychiatric diseases.代谢型谷氨酸受体5负变构调节剂:2-氯-4-[1-(4-氟苯基)-2,5-二甲基-1H-咪唑-4-基乙炔基]吡啶(巴西谷氨酸,RO4917523)的发现,一种有前景的治疗精神疾病的新型药物。
J Med Chem. 2015 Feb 12;58(3):1358-71. doi: 10.1021/jm501642c. Epub 2015 Feb 2.
7
Metabotropic glutamate receptor 5 as drug target for Fragile X syndrome.代谢型谷氨酸受体5作为脆性X综合征的药物靶点。
Curr Opin Pharmacol. 2015 Feb;20:124-34. doi: 10.1016/j.coph.2014.11.004. Epub 2014 Dec 2.
8
Longitudinal profiles of adaptive behavior in fragile X syndrome.脆性X综合征中适应性行为的纵向概况。
Pediatrics. 2014 Aug;134(2):315-24. doi: 10.1542/peds.2013-3990.
9
Aberrant face and gaze habituation in fragile x syndrome.脆性X综合征中的异常面部和注视习惯化
Am J Psychiatry. 2014 Oct;171(10):1099-106. doi: 10.1176/appi.ajp.2014.13111464.
10
Topological methods reveal high and low functioning neuro-phenotypes within fragile X syndrome.拓扑学方法揭示了脆性X综合征中高功能和低功能神经表型。
Hum Brain Mapp. 2014 Sep;35(9):4904-15. doi: 10.1002/hbm.22521. Epub 2014 Apr 15.

脆性 X 综合征青少年及青年期的神经解剖学异常。

Neuroanatomical abnormalities in fragile X syndrome during the adolescent and young adult years.

机构信息

Center for Interdisciplinary Brain Sciences Research, Stanford University, 401 Quarry Road, Stanford, CA 94305-5795, USA.

Center for Interdisciplinary Brain Sciences Research, Stanford University, 401 Quarry Road, Stanford, CA 94305-5795, USA.

出版信息

J Psychiatr Res. 2018 Dec;107:138-144. doi: 10.1016/j.jpsychires.2018.10.014. Epub 2018 Oct 25.

DOI:10.1016/j.jpsychires.2018.10.014
PMID:30408626
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6249038/
Abstract

Abnormal brain development and cognitive dysfunction have been reported both in children and in adults with fragile X syndrome (FXS). However, few studies have examined neuroanatomical abnormalities in FXS during adolescence. In this study we focus on adolescent subjects with FXS (N = 54) as compared to age- and sex-matched subjects with idiopathic intellectual disability (Comparison Group) (N = 32), to examine neuroanatomical differences during this developmental period. Brain structure was assessed with voxel-based morphometry and independent groups t-test in SPM8 software. Results showed that the FXS group, relative to the comparison group, had significantly larger gray matter volume (GMV) in only one region: the bilateral caudate nucleus, but have smaller GMV in several regions including bilateral medial frontal, pregenual cingulate, gyrus rectus, insula, and superior temporal gyrus. Group differences also were noted in white matter regions. Within the FXS group, lower FMRP levels were associated with less GMV in several regions including cerebellum and gyrus rectus, and less white matter volume (WMV) in pregenual cingulate, middle frontal gyrus, and other regions. Lower full scale IQ within the FXS group was associated with larger right caudate nucleus GMV. In conclusion, adolescents and young adults with FXS demonstrate neuroanatomical abnormalities consistent with those previously reported in children and adults with FXS. These brain variations likely result from reduced FMRP during early neurodevelopment and mediate downstream deleterious effects on cognitive function.

摘要

脆性 X 综合征(FXS)患者既有儿童期也有成年期的脑发育异常和认知功能障碍的报道。然而,很少有研究检查过 FXS 青少年时期的神经解剖异常。在这项研究中,我们重点关注 FXS 的青少年受试者(N=54),并与年龄和性别匹配的特发性智力障碍受试者(对照组)(N=32)进行比较,以检查这一发育阶段的神经解剖差异。使用 SPM8 软件的基于体素的形态测量法和独立样本 t 检验来评估大脑结构。结果显示,与对照组相比,FXS 组仅在两个尾状核区域的灰质体积(GMV)显著增大,但在多个区域(包括双侧额内侧回、扣带回前回、直回、岛叶和颞上回)的 GMV 减小。在白质区域也观察到了组间差异。在 FXS 组内,较低的 FMRP 水平与几个区域(包括小脑和直回)的 GMV 减少,以及扣带回前回、额中回和其他区域的白质体积(WMV)减少有关。在 FXS 组内,全量表智商较低与右侧尾状核 GMV 增大有关。总之,FXS 的青少年和年轻成年人表现出与以前报道的 FXS 儿童和成人一致的神经解剖异常。这些脑变化可能是由于早期神经发育过程中 FMRP 减少,并对认知功能产生下游的有害影响所致。