Evidence map›Paper›PMID 31263778›Full record

ArticleCommunications biology2019

Metabolome signature of autism in the human prefrontal cortex.

Ilia Kurochkin, Ekaterina Khrameeva, Anna Tkachev, Vita Stepanova, Anna Vanyushkina, Elena Stekolshchikova, Qian Li, Dmitry Zubkov, Polina Shichkova, Tobias Halene and 4 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
4.5field-weighted citation impact, top 5% 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

39 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 citations in OpenAlex.

  1. Pooled it
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  7. Metabolomic changes in children with autism.World journal of clinical pediatrics · 2024
    Article
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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

14 authors at 5 institutions in 4 countries.

Ilia Kurochkin *1Center for Neurobiology and Brain Restoration, Skolkovo Institute of Science and Technology, Moscow, 121205 Russia.
Ekaterina Khrameeva *1Center for Neurobiology and Brain Restoration, Skolkovo Institute of Science and Technology, Moscow, 121205 Russia.
Anna Tkachev1Center for Neurobiology and Brain Restoration, Skolkovo Institute of Science and Technology, Moscow, 121205 Russia.
Vita Stepanova1Center for Neurobiology and Brain Restoration, Skolkovo Institute of Science and Technology, Moscow, 121205 Russia.
Anna Vanyushkina1Center for Neurobiology and Brain Restoration, Skolkovo Institute of Science and Technology, Moscow, 121205 Russia.
Elena Stekolshchikova1Center for Neurobiology and Brain Restoration, Skolkovo Institute of Science and Technology, Moscow, 121205 Russia.
Qian Li3CAS Key Laboratory of Computational Biology, CAS-MPG Partner Institute for Computational Biology, 320 Yue Yang Road, 200031 Shanghai, China.
Dmitry Zubkov1Center for Neurobiology and Brain Restoration, Skolkovo Institute of Science and Technology, Moscow, 121205 Russia.
Polina Shichkova1Center for Neurobiology and Brain Restoration, Skolkovo Institute of Science and Technology, Moscow, 121205 Russia.
Tobias Halene4Department of Psychiatry and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029 USA.
Lothar Willmitzer5Max Planck Institute for Molecular Plant Physiology, Am Mühlenberg 1, Potsdam, 14476 Germany.
Patrick Giavalisco6Max Planck Institute for Biology of Ageing, Cologne, 50931 Germany.
Schahram Akbarian4Department of Psychiatry and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029 USA.ORCID 0000-0001-7700-0891
Philipp Khaitovich1Center for Neurobiology and Brain Restoration, Skolkovo Institute of Science and Technology, Moscow, 121205 Russia.
Skolkovo Institute of Science and Technology · RUAllen Institute for Brain Science · USCenter for Excellence in Molecular Cell Science · CNMax Planck Institute for Biology of Ageing · DEMax Planck Institute of Molecular Plant Physiology · DE

Funding

A National Chimpanzee Brain ResourceR24NS092988 · NINDS · GEORGE WASHINGTON UNIVERSITY · PI SHERWOOD, CHESTER · 2015 to 2018
$969k
NINDS NIH HHS R24 NS092988
6 · The paper itself

Abstract

Autism spectrum disorder (ASD) is a common neurodevelopmental disorder with yet incompletely uncovered molecular determinants. Alterations in the abundance of low molecular weight compounds (metabolites) in ASD could add to our understanding of the disease. Indeed, such alterations take place in the urine, plasma and cerebellum of ASD individuals. In this work, we investigated mass-spectrometric signal intensities of 1,366 metabolites in the prefrontal cortex grey matter of 32 ASD and 40 control individuals. 15% of these metabolites showed significantly different intensities in ASD and clustered in 16 metabolic pathways. Of them, ten pathways were altered in urine and blood of ASD individuals (Fisher test,

Indexed as

MetabolomeAnimalsAutistic DisorderEvolution, MolecularGray MatterHumansMacaca mulattaMachine LearningMetabolic Networks and PathwaysPan troglodytesPrefrontal CortexAutism spectrum disordersMetabolomicsMolecular neuroscience

Identifiers

PMID31263778
PMCPMC6588695
OpenAlexW2951672526

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.