Evidence map›Paper›PMID 36973347›Full record

ArticleMolecular psychiatry2023

Altered behavior, brain structure, and neurometabolites in a rat model of autism-specific maternal autoantibody exposure.

Matthew R Bruce, Amalie C M Couch, Simone Grant, Janna McLellan, Katherine Ku, Christina Chang, Angelica Bachman, Matthew Matson, Robert F Berman, Richard J Maddock and 8 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular psychiatry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 3 institutions in 2 countries.

Matthew R BruceDepartment of Internal Medicine, Division of Rheumatology, Allergy, and Clinical Immunology, University of California, Davis, CA, USA.ORCID 0000-0002-6943-1410
Amalie C M CouchDepartment of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
Simone GrantDepartment of Psychiatry and Behavioral Sciences, University of California, Davis, CA, USA.
Janna McLellanDepartment of Internal Medicine, Division of Rheumatology, Allergy, and Clinical Immunology, University of California, Davis, CA, USA.
Katherine KuDepartment of Psychiatry and Behavioral Sciences, University of California, Davis, CA, USA.
Christina ChangDepartment of Psychiatry and Behavioral Sciences, University of California, Davis, CA, USA.
Angelica BachmanDepartment of Psychiatry and Behavioral Sciences, University of California, Davis, CA, USA.
Matthew MatsonDepartment of Psychiatry and Behavioral Sciences, University of California, Davis, CA, USA.
Robert F BermanDepartment of Neurological Surgery, University of California, Davis, CA, USA.
Richard J MaddockDepartment of Psychiatry and Behavioral Sciences, University of California, Davis, CA, USA.ORCID 0000-0001-6392-5519
Douglas RowlandCenter for Molecular and Genomic Imaging, University of California, Davis, CA, USA.ORCID 0000-0001-8059-6905
Eugene KimDepartment of Neuroimaging, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.ORCID 0000-0003-0066-7051
Matthew D PonziniDepartment of Neuroimaging, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
Danielle HarveyDepartment of Public Health Sciences, University of California, Davis, CA, USA.
Sandra L TaylorDepartment of Public Health Sciences, University of California, Davis, CA, USA.
Anthony C Vernon *Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.ORCID 0000-0001-7305-1069
Melissa D Bauman *Department of Psychiatry and Behavioral Sciences, University of California, Davis, CA, USA.
Judy Van de WaterDepartment of Internal Medicine, Division of Rheumatology, Allergy, and Clinical Immunology, University of California, Davis, CA, USA. javandewater@ucdavis.edu.ORCID 0000-0003-1193-5875
University of California, Davis · USKing's College London · GBNeurological Surgery · US

Funding

THE CHARGE STUDY: CHILDHOOD AUTISM RISKS FROM GENETICS AND THE ENVIRONMENT - ADMINISTRATIVE SUPPLEMENTR01ES015359 · NIEHS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HERTZ-PICCIOTTO, IRVA · 2007 to 2019
$13.8M
UC Davis Center for Children's Environmental Health (CCEH)P01ES011269 · NIEHS · UNIVERSITY OF CALIFORNIA DAVIS · PI VAN DE WATER, JUDY A. · 2001 to 2018
$12.5M
Research Project: Pathologic Significance of Maternal AutoantibodiesP50HD103526 · NICHD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LEONARD J. ABBEDUTO, Melissa Dawn Bauman · 2020 to 2026
$9.7M
Learning, Memory, and Plasticity (LaMP) Training ProgramT32MH112507 · NIMH · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Karen Zito · 2017 to 2026
$2.4M
Medical Research Council MR/W006251/1NICHD NIH HHS P50 HD103526NIEHS NIH HHS P01 ES011269NIEHS NIH HHS R01 ES015359NIMH NIH HHS T32 MH112507
6 · The paper itself

Abstract

Maternal immune dysregulation is a prenatal risk factor for autism spectrum disorder (ASD). Importantly, a clinically relevant connection exists between inflammation and metabolic stress that can result in aberrant cytokine signaling and autoimmunity. In this study we examined the potential for maternal autoantibodies (aAbs) to disrupt metabolic signaling and induce neuroanatomical changes in the brains of exposed offspring. To accomplish this, we developed a model of maternal aAb exposure in rats based on the clinical phenomenon of maternal autoantibody-related ASD (MAR-ASD). Following confirmation of aAb production in rat dams and antigen-specific immunoglobulin G (IgG) transfer to offspring, we assessed offspring behavior and brain structure longitudinally. MAR-ASD rat offspring displayed a reduction in pup ultrasonic vocalizations and a pronounced deficit in social play behavior when allowed to freely interact with a novel partner. Additionally, longitudinal in vivo structural magnetic resonance imaging (sMRI) at postnatal day 30 (PND30) and PND70, conducted in a separate cohort of animals, revealed sex-specific differences in total and regional brain volume. Treatment-specific effects by region appeared to converge on midbrain and cerebellar structures in MAR-ASD offspring. Simultaneously, in vivo

Indexed as

Autism Spectrum DisorderAutistic DisorderPrenatal Exposure Delayed EffectsAnimalsAutoantibodiesBrainFemaleHumansMaleMaternal ExposurePregnancyRatsAutoantibodies

Identifiers

PMID36973347
PMCPMC10575787
OpenAlexW4360991794

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.