Evidence map›Paper›PMID 30381433›Full record

ReviewThe Journal of neuroscience : the official journal of the Society for Neuroscience2018

Defining Dysbiosis in Disorders of Movement and Motivation.

Christopher T Fields, Timothy R Sampson, Annadora J Bruce-Keller, Drew D Kiraly, Elaine Y Hsiao, Geert J de Vries

Open access · bronzeAbstract readReview
In one paragraph

Review in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

9 citing papers in PubMed, 19 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

6 authors at 5 institutions in 1 country.

Christopher T FieldsNeuroscience Institute, Georgia State University, Atlanta, Georgia 30303, cfields18@student.gsu.edu.ORCID 0000-0002-2054-7316
Timothy R SampsonDivision of Biology & Biological Engineering, California Institute of Technology, Pasadena, California 91125.
Annadora J Bruce-KellerPennington Biomedical Research Center, Louisiana State University System, Baton Rouge, Louisiana 70808.
Drew D KiralyDepartments of Psychiatry & Neuroscience, Friedman Brain Institute, Icahn School of Medicine, New York, New York 10029, and.ORCID 0000-0002-4818-5169
Elaine Y HsiaoDepartment of Integrative Biology and Physiology, University of California-Los Angeles, Los Angeles, California 90095.
Geert J de VriesNeuroscience Institute, Georgia State University, Atlanta, Georgia 30303.
Georgia State University · USAllen Institute for Brain Science · USCalifornia Institute of Technology · USPennington Biomedical Research Center · USUniversity of California, Los Angeles · US

Funding

Uncovering microbial modulators of neuroactive molecules as novel therapeutics.DP5OD017924 · OD · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI HSIAO, ELAINE · 2013 to 2017
$1.9M
Dissecting the role of granulocyte-colony stimulating factor in cocaine-mediated behavioral plasticityK08DA044308 · NIDA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI KIRALY, DREW · 2017 to 2021
$938k
Microbiota and Neural Circuits controlling Social BehaviorR21MH108345 · NIMH · GEORGIA STATE UNIVERSITY · PI DE VRIES, GEERT J., FORGER, NANCY G · 2016 to 2017
$416k
Gut Microbiota in the Control of Neurobehavioral Function in MiceR21MH110117 · NIMH · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI BRUCE-KELLER, ANNADORA J · 2016 to 2017
$407k
The Role of Intestinal Epithelial TLR4 in Anxiety BehaviorR36MH112369 · NIMH · GEORGIA STATE UNIVERSITY · PI FIELDS, CHRISTOPHER · 2017 to 2018
$83k
Functional Role of IL-6 in Fetal Brain Development and Abnormal BehaviorF31MH090749 · NIMH · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI HSIAO, ELAINE · 2011 to 2012
$64k
NIDA NIH HHS K08 DA044308NIH HHS DP5 OD017924NIMH NIH HHS F31 MH090749NIMH NIH HHS R21 MH108345NIMH NIH HHS R21 MH110117NIMH NIH HHS R36 MH112369
6 · The paper itself

Abstract

The gut microbiota has emerged as a critical player in shaping and modulating brain function and has been shown to influence numerous behaviors, including anxiety and depression-like behaviors, sociability, and cognition. However, the effects of the gut microbiota on specific disorders associated with thalamo-cortico-basal ganglia circuits, ranging from compulsive behavior and addiction to altered sensation and motor output, are only recently being explored. Wholesale depletion and alteration of gut microbial communities in rodent models of disorders, such as Parkinson's disease, autism, and addiction, robustly affect movement and motivated behavior. A new frontier therefore lies in identifying specific microbial alterations that affect these behaviors and understanding the underlying mechanisms of action. Comparing alterations in gut microbiota across multiple basal-ganglia associated disease states allows for identification of common mechanistic pathways that may interact with distinct environmental and genetic risk factors to produce disease-specific outcomes.

Indexed as

AnimalsBrainDysbiosisGastrointestinal MicrobiomeHumansMental DisordersMotivationMovementaddictionbasal gangliacompulsive behaviorgut microbiotamotor functionParkinson's

Identifiers

PMID30381433
PMCPMC6209841
OpenAlexW2899457671

What OpenQuestion holds

Textmetadata
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.