Literature DB >> 30231625

Sensory Processing Phenotypes in Fragile X Syndrome.

Maham Rais1,2, Devin K Binder1,2,3, Khaleel A Razak2,3,4, Iryna M Ethell1,2,3.   

Abstract

Fragile X syndrome (FXS) is a neurodevelopmental disorder that causes intellectual disability. It is a leading known genetic cause of autism. In addition to cognitive, social, and communication deficits, humans with FXS demonstrate abnormal sensory processing including sensory hypersensitivity. Sensory hypersensitivity commonly manifests as auditory, tactile, or visual defensiveness or avoidance. Clinical, behavioral, and electrophysiological studies consistently show auditory hypersensitivity, impaired habituation to repeated sounds, and reduced auditory attention in humans with FXS. Children with FXS also exhibit significant visuospatial impairments. Studies in infants and toddlers with FXS have documented impairments in processing texture-defined motion stimuli, temporal flicker, perceiving ordinal numerical sequence, and the ability to maintain the identity of dynamic object information during occlusion. Consistent with the observations in humans with FXS, fragile X mental retardation 1 ( Fmr1) gene knockout (KO) rodent models of FXS also show seizures, abnormal visual-evoked responses, auditory hypersensitivity, and abnormal processing at multiple levels of the auditory system, including altered acoustic startle responses. Among other sensory symptoms, individuals with FXS exhibit tactile defensiveness. Fmr1 KO mice also show impaired encoding of tactile stimulation frequency and larger size of receptive fields in the somatosensory cortex. Since sensory deficits are relatively more tractable from circuit mechanisms and developmental perspectives than more complex social behaviors, the focus of this review is on clinical, functional, and structural studies that outline the auditory, visual, and somatosensory processing deficits in FXS. The similarities in sensory phenotypes between humans with FXS and animal models suggest a likely conservation of basic sensory processing circuits across species and may provide a translational platform to not just develop biomarkers but also to understand underlying mechanisms. We argue that preclinical studies in animal models of FXS can facilitate the ongoing search for new therapeutic approaches in FXS by understanding mechanisms of basic sensory processing circuits and behaviors that are conserved across species.

Entities:  

Keywords:  autism spectrum disorders; fragile X syndrome; neurodevelopmental disorders; sensory hypersensitivity

Mesh:

Substances:

Year:  2018        PMID: 30231625      PMCID: PMC6149018          DOI: 10.1177/1759091418801092

Source DB:  PubMed          Journal:  ASN Neuro        ISSN: 1759-0914            Impact factor:   4.146


  224 in total

1.  Activation of the extracellular signal-regulated kinase 2 by metabotropic glutamate receptors.

Authors:  F Ferraguti; B Baldani-Guerra; M Corsi; S Nakanishi; C Corti
Journal:  Eur J Neurosci       Date:  1999-06       Impact factor: 3.386

2.  Auditory and visual cortical activity during selective attention in fragile X syndrome: a cascade of processing deficiencies.

Authors:  M J W Van der Molen; M W Van der Molen; K R Ridderinkhof; B C J Hamel; L M G Curfs; G J A Ramakers
Journal:  Clin Neurophysiol       Date:  2011-09-29       Impact factor: 3.708

3.  P3 abnormality in fragile X syndrome.

Authors:  D M St Clair; D H Blackwood; C J Oliver; P Dickens
Journal:  Biol Psychiatry       Date:  1987-03       Impact factor: 13.382

4.  Fmrp is required for the establishment of the startle response during the critical period of auditory development.

Authors:  Seong-Wook Yun; Jimcy Platholi; Maria Sol Flaherty; Weimin Fu; Andreas H Kottmann; Miklos Toth
Journal:  Brain Res       Date:  2006-08-02       Impact factor: 3.252

5.  Audiogenic seizure susceptibility is reduced in fragile X knockout mice after introduction of FMR1 transgenes.

Authors:  Sebastiano A Musumeci; Giuseppe Calabrese; Carmela M Bonaccorso; Simona D'Antoni; Judith R Brouwer; Cathy E Bakker; Maurizio Elia; Raffaele Ferri; David L Nelson; Ben A Oostra; Maria Vincenza Catania
Journal:  Exp Neurol       Date:  2006-09-27       Impact factor: 5.330

6.  Contrast detection in infants with fragile X syndrome.

Authors:  F Farzin; D Whitney; R J Hagerman; S M Rivera
Journal:  Vision Res       Date:  2008-05-23       Impact factor: 1.886

7.  Differential impact of the FMR1 gene on visual processing in fragile X syndrome.

Authors:  Cary S Kogan; Isabelle Boutet; Kim Cornish; Shahin Zangenehpour; Kathy T Mullen; Jeanette J A Holden; Vazken M Der Kaloustian; Eva Andermann; Avi Chaudhuri
Journal:  Brain       Date:  2004-01-21       Impact factor: 13.501

8.  Disrupted Cortical State Regulation in a Rat Model of Fragile X Syndrome.

Authors:  Julia Berzhanskaya; Marnie A Phillips; Alexis Gorin; Chongxi Lai; Jing Shen; Matthew T Colonnese
Journal:  Cereb Cortex       Date:  2017-02-01       Impact factor: 5.357

9.  Extracellular signal-regulated protein kinase activation is required for metabotropic glutamate receptor-dependent long-term depression in hippocampal area CA1.

Authors:  Sean M Gallagher; Christine A Daly; Mark F Bear; Kimberly M Huber
Journal:  J Neurosci       Date:  2004-05-19       Impact factor: 6.167

Review 10.  Minocycline-induced pigmentation. Incidence, prevention and management.

Authors:  D Eisen; M D Hakim
Journal:  Drug Saf       Date:  1998-06       Impact factor: 5.606

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  35 in total

1.  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

2.  Genetic reduction of MMP-9 in the Fmr1 KO mouse partially rescues prepulse inhibition of acoustic startle response.

Authors:  Jamiela Kokash; Erin M Alderson; Sarah M Reinhard; Cynthia A Crawford; Devin K Binder; Iryna M Ethell; Khaleel A Razak
Journal:  Brain Res       Date:  2019-05-22       Impact factor: 3.252

3.  Abnormal development of auditory responses in the inferior colliculus of a mouse model of Fragile X Syndrome.

Authors:  Anna O Nguyen; Devin K Binder; Iryna M Ethell; Khaleel A Razak
Journal:  J Neurophysiol       Date:  2020-04-22       Impact factor: 2.714

4.  Developmental Changes in EEG Phenotypes in a Mouse Model of Fragile X Syndrome.

Authors:  Teresa H Wen; Jonathan W Lovelace; Iryna M Ethell; Devin K Binder; Khaleel A Razak
Journal:  Neuroscience       Date:  2018-12-05       Impact factor: 3.590

5.  Clinical and behavioural features of SYNGAP1-related intellectual disability: a parent and caregiver description.

Authors:  Damien Wright; Aisling Kenny; Sarah Eley; Andrew G McKechanie; Andrew C Stanfield
Journal:  J Neurodev Disord       Date:  2022-06-02       Impact factor: 4.074

6.  Acute pharmacological inhibition of matrix metalloproteinase-9 activity during development restores perineuronal net formation and normalizes auditory processing in Fmr1 KO mice.

Authors:  Patricia S Pirbhoy; Maham Rais; Jonathan W Lovelace; Walker Woodard; Khaleel A Razak; Devin K Binder; Iryna M Ethell
Journal:  J Neurochem       Date:  2020-06-08       Impact factor: 5.372

Review 7.  Mechanisms underlying auditory processing deficits in Fragile X syndrome.

Authors:  Elizabeth A McCullagh; Sarah E Rotschafer; Benjamin D Auerbach; Achim Klug; Leonard K Kaczmarek; Karina S Cramer; Randy J Kulesza; Khaleel A Razak; Jonathan W Lovelace; Yong Lu; Ursula Koch; Yuan Wang
Journal:  FASEB J       Date:  2020-02-10       Impact factor: 5.191

8.  FMRP regulates the subcellular distribution of cortical dendritic spine density in a non-cell-autonomous manner.

Authors:  Katherine M Bland; Adam Aharon; Eden L Widener; M Irene Song; Zachary O Casey; Yi Zuo; George S Vidal
Journal:  Neurobiol Dis       Date:  2021-01-06       Impact factor: 5.996

9.  GABAA Alpha 2,3 Modulation Improves Select Phenotypes in a Mouse Model of Fragile X Syndrome.

Authors:  Tori L Schaefer; Amy A Ashworth; Durgesh Tiwari; Madison P Tomasek; Emma V Parkins; Angela R White; Andrew Snider; Matthew H Davenport; Lindsay M Grainger; Robert A Becker; Chandler K Robinson; Rishav Mukherjee; Michael T Williams; Jay R Gibson; Kimberly M Huber; Christina Gross; Craig A Erickson
Journal:  Front Psychiatry       Date:  2021-05-21       Impact factor: 4.157

10.  Impaired Adaptation and Laminar Processing of the Oddball Paradigm in the Primary Visual Cortex of Fmr1 KO Mouse.

Authors:  Alexandr Pak; Samuel T Kissinger; Alexander A Chubykin
Journal:  Front Cell Neurosci       Date:  2021-05-19       Impact factor: 5.505

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