Evidence map›Paper›PMID 33994977›Full record

ArticleFrontiers in human neuroscience2021

Early Life Stress and the Fate of Kynurenine Pathway Metabolites.

Jeremy D Coplan, Roza George, Shariful A Syed, Annalam V Rozenboym, Jean E Tang, Sasha L Fulton, Tarique D Perera

Abstract read
In one paragraph

Article in Frontiers in human neuroscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

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  11. Review
  12. PTSD, Immune System, and Inflammation.Advances in experimental medicine and biology · 2023
    Article
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

7 authors.

Jeremy D CoplanDepartment of Psychiatry, State University of New York Downstate Medical Center, Brooklyn, NY, United States.
Roza GeorgeFirstox Laboratories, Irving, TX, United States.
Shariful A SyedDepartment of Psychiatry, Yale University School of Medicine, New Haven, CT, United States.
Annalam V RozenboymDepartment of Biological Sciences, Kingsborough Community College, CUNY, Brooklyn, NY, United States.
Jean E TangTeachers College, Columbia University, New York, NY, United States.
Sasha L FultonIcahn School of Medicine at Mount Sinai, New York, NY, United States.
Tarique D PereraContemporary Care, Danbury, CT, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Early life stress (ELS) precedes alterations to neuro-immune activation, which may mediate an increased risk for stress-related psychiatric disorders, potentially through alterations of central kynurenine pathway (KP) metabolites, the latter being relatively unexplored. We hypothesized that ELS in a non-human primate model would lead to a reduction of neuroprotective and increases of neurotoxic KP metabolites. Twelve adult female bonnet macaques reared under conditions of maternal variable foraging demand (VFD) were compared to 27 age- and weight-matched non-VFD-exposed female controls. Baseline behavioral observations of social affiliation were taken over a 12-week period followed by the first cerebrospinal fluid (CSF) sample. Subjects were then either exposed to a 12-week repeated separation paradigm (RSP) or assigned to a "no-RSP" condition followed by a second CSF. We used high-performance liquid chromatography for kynurenine (KYN), tryptophan, 5-hydroxyindoleacetic acid, kynurenic acid (KYNA), and anthranilic acid (ANTH) as a proxy for quinolinic acid determination. At baseline, social affiliation scores were reduced in VFD-reared versus control subjects. CSF log KYNA and log KYNA/KYN ratio were lower in VFD-reared versus control subjects. CSF log KYNA/KYN was positively correlated with CSF log ANTH in VFD only (

Indexed as

Anthranilic acid (AA)childhood adversitiesearly life stress (ELS)kynurenic acid (KYNA)kynurenine (KYN)Major depressive disordersNeuroprotectionnon human primate

Identifiers

PMID33994977
PMCPMC8117097

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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.