Evidence map›Paper›PMID 38071324›Full record

ArticleTranslational psychiatry2023

Impact of IDO activation and alterations in the kynurenine pathway on hyperserotonemia, NAD

Jean-Marie Launay, Richard Delorme, Cécile Pagan, Jacques Callebert, Marion Leboyer, Nicolas Vodovar

Open access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

21 citing papers in PubMed, 20 citations in OpenAlex.

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  18. Autophagy-NADFrontiers in molecular biosciences · 2025
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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 3 institutions in 1 country.

Jean-Marie LaunayUniversité Paris Cité and Inserm UMR-S 942 MASCOT, Paris, France. jean-marie.launay@inserm.fr.ORCID 0000-0003-4809-1020
Richard DelormeUniversité Paris Cité and Child and Adolescent Psychiatry, Robert Debré Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.
Cécile PaganService de Biochimie et Biologie Moléculaire, Centre de Biologie et de Pathologie Est, Hospices Civils de Lyon, 69500, Bron, France.
Jacques CallebertUniversité Paris Cité and Inserm UMR-S 942 MASCOT, Paris, France.
Marion LeboyerUniversité Paris Est Créteil and Inserm U955, IMRB, Translational Neuropsychiatry, Créteil, France.ORCID 0000-0001-5473-3697
Nicolas VodovarUniversité Paris Cité and Inserm UMR-S 942 MASCOT, Paris, France. nicolas.vodovar@inserm.fr.ORCID 0000-0001-8087-387X
Inserm · FRHospices Civils de Lyon · FRUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hyperserotonemia is the most replicated biochemical anomaly associated with autism spectrum disorder (ASD) and has been reported in 35-46% of individuals with ASD. Serotonin is synthesised from the essential amino acid tryptophan (TRP). However, the main catabolic route of TRP is the kynurenine pathway (KP), which competes with serotonin synthesis when indoleamine dioxygenase (IDO) is activated. Using the same cohort of individuals with ASD, we used to report extensive studies of the serotonin/melatonin pathway, and found increased kynurenine (KYN), suggesting IDO activation in 58.7% of individuals with ASD (159/271), supported by a strong negative correlation between KYN/TRP ratio and miR-153-3p plasma levels, which negatively regulates IDO. IDO activation was associated with normoserotonemia, suggesting that IDO activation could mask hyperserotonemia which meant that hyperserotonemia, if not masked by IDO activation, could be present in ~94% of individuals with ASD. We also identified several KP alterations, independent of IDO status. We observed a decrease in the activity of 3-hydroxyanthranilate dioxygenase which translated into the accumulation of the aryl hydrocarbon receptor (AhR) selective ligand cinnabarinic acid, itself strongly positively correlated with the AhR target stanniocalcin 2. We also found a deficit in NAD

Indexed as

Autism Spectrum DisorderDioxygenasesMicroRNAsNeuropeptidesHumansKynurenineNADReceptors, Aryl HydrocarbonSerotoninTryptophanDioxygenasesKynurenineMicroRNAsMIRN153 microRNA, humanNADNeuropeptidesReceptors, Aryl HydrocarbonSerotoninTryptophan

Identifiers

PMID38071324
PMCPMC10710433
OpenAlexW4389509087

What OpenQuestion holds

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Registered trials

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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.