Evidence map›Paper›PMID 29184200›Full record

ArticleNature neuroscience2017

Altered cerebellar connectivity in autism and cerebellar-mediated rescue of autism-related behaviors in mice.

Catherine J Stoodley, Anila M D'Mello, Jacob Ellegood, Vikram Jakkamsetti, Pei Liu, Mary Beth Nebel, Jennifer M Gibson, Elyza Kelly, Fantao Meng, Christopher A Cano and 4 more

Erratum issuedAbstract read
In one paragraph

Article in Nature neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 209 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
209citing papers in PubMed, 4 pooled it
18.1field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

209 citing papers in PubMed, 4 syntheses or guidelines pooled it, 399 citations in OpenAlex.

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149 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 5 institutions in 2 countries.

Catherine J StoodleyDepartment of Psychology and Center for Behavioral Neuroscience, American University, Washington, DC, USA. stoodley@american.edu.ORCID http://orcid.org/0000-0003-2629-0213
Anila M D'MelloDepartment of Psychology and Center for Behavioral Neuroscience, American University, Washington, DC, USA.ORCID http://orcid.org/0000-0001-6653-7802
Jacob EllegoodToronto Mouse Imaging Centre, Hospital for Sick Kids, Toronto, Canada.ORCID http://orcid.org/0000-0003-1504-3321
Vikram JakkamsettiThe Department of Neurology and Neurotherapeutics, University of Texas Southwestern Medical Center, Dallas, Texas, USA.ORCID http://orcid.org/0000-0001-6524-2893
Pei LiuThe Department of Neurology and Neurotherapeutics, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Mary Beth NebelCenter for Neurodevelopmental and Imaging Research, Kennedy Krieger Institute, Baltimore, Maryland, USA.ORCID http://orcid.org/0000-0003-0185-3382
Jennifer M GibsonThe Department of Neurology and Neurotherapeutics, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Elyza KellyThe Department of Neurology and Neurotherapeutics, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Fantao MengThe Department of Neurology and Neurotherapeutics, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Christopher A CanoThe Department of Neurology and Neurotherapeutics, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Juan M PascualThe Department of Neurology and Neurotherapeutics, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Stewart H MostofskyCenter for Neurodevelopmental and Imaging Research, Kennedy Krieger Institute, Baltimore, Maryland, USA.
Jason P LerchToronto Mouse Imaging Centre, Hospital for Sick Kids, Toronto, Canada.
Peter T TsaiThe Department of Neurology and Neurotherapeutics, University of Texas Southwestern Medical Center, Dallas, Texas, USA. peter.tsai@utsouthwestern.edu.ORCID http://orcid.org/0000-0002-0729-9688
The University of Texas Southwestern Medical Center · USAmerican University · USHospital for Sick Children · CAKennedy Krieger Institute · USSouthwestern Medical Center · US

Funding

Neurology of Deficient Response Control in ADHDR01MH085328 · NIMH · HUGO W. MOSER RES INST KENNEDY KRIEGER · PI MOSTOFSKY, STEWART H · 2009 to 2019
$7.3M
Basic Science Training Program in Drug Abuse ResearchT32DA007290 · NIDA · YALE UNIVERSITY · PI SELF, DAVID W · 1992 to 2017
$6.7M
Anomalous Motor Physiology In ADHDR01MH078160 · NIMH · HUGO W. MOSER RES INST KENNEDY KRIEGER · PI MOSTOFSKY, STEWART H · 2006 to 2024
$5.8M
Motor Skill Learning in AutismR01NS048527 · NINDS · HUGO W. MOSER RES INST KENNEDY KRIEGER · PI MOSTOFSKY, STEWART H · 2005 to 2012
$2.9M
Mechanisms underlying the Cerebellar Contribution to Autism in Mouse Models of Tuberous Sclerosis ComplexK08NS083733 · NINDS · UT SOUTHWESTERN MEDICAL CENTER · PI TSAI, PETER T. · 2013 to 2017
$952k
Visual-Motor Development in Infants at High Risk for AutismK01MH109766 · NIMH · HUGO W. MOSER RES INST KENNEDY KRIEGER · PI NEBEL, MARY BETH · 2016 to 2020
$753k
Cerebellum and autism: Neural mechanisms and modulation of predictive processingR15MH106957 · NIMH · AMERICAN UNIVERSITY · PI STOODLEY, CATHERINE J. · 2015 to 2015
$403k
NIMH NIH HHS K01 MH109766NIMH NIH HHS R01 MH078160NIMH NIH HHS R01 MH085328NIMH NIH HHS R15 MH106957NINDS NIH HHS K08 NS083733NINDS NIH HHS R01 NS048527
6 · The paper itself

Abstract

Cerebellar abnormalities, particularly in Right Crus I (RCrusI), are consistently reported in autism spectrum disorders (ASD). Although RCrusI is functionally connected with ASD-implicated circuits, the contribution of RCrusI dysfunction to ASD remains unclear. Here neuromodulation of RCrusI in neurotypical humans resulted in altered functional connectivity with the inferior parietal lobule, and children with ASD showed atypical functional connectivity in this circuit. Atypical RCrusI-inferior parietal lobule structural connectivity was also evident in the Purkinje neuron (PN) TscI ASD mouse model. Additionally, chemogenetically mediated inhibition of RCrusI PN activity in mice was sufficient to generate ASD-related social, repetitive, and restricted behaviors, while stimulation of RCrusI PNs rescued social impairment in the PN TscI ASD mouse model. Together, these studies reveal important roles for RCrusI in ASD-related behaviors. Further, the rescue of social behaviors in an ASD mouse model suggests that investigation of the therapeutic potential of cerebellar neuromodulation in ASD may be warranted.

Indexed as

AnimalsAutism Spectrum DisorderBehavior, AnimalCerebellumChildFemaleHumansMagnetic Resonance ImagingMaleMaze LearningMiceMice, TransgenicNeural PathwaysPurkinje CellsRestSmell

Identifiers

PMID29184200
PMCPMC5867894
OpenAlexW2767035585

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.