Evidence map›Paper›PMID 25566007›Full record

ArticleFrontiers in behavioral neuroscience2014

Elevated cerebrospinal fluid 5-hydroxyindoleacetic acid in macaques following early life stress and inverse association with hippocampal volume: preliminary implications for serotonin-related function in mood and anxiety disorders.

Jeremy D Coplan, Sasha L Fulton, Wade Reiner, Andrea Jackowski, Venkatesh Panthangi, Tarique D Perera, Jack M Gorman, Yung-Yu Huang, Cheuk Y Tang, Patrick R Hof and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in behavioral neuroscience, 2014. 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
1.3field-weighted citation impact, top 20% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

  1. Trial
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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

15 authors at 7 institutions in 1 country.

Jeremy D CoplanNonhuman Primate Laboratory, Department of Psychiatry and Behavioral Sciences, Downstate Medical Center, State University of New York Brooklyn, NY, USA.
Sasha L FultonGeriatric Psychiatry, New York State Psychiatric Institute New York, NY, USA.
Wade ReinerCollege of Medicine, State University of New York Downstate Medical Center Brooklyn, NY, USA.
Andrea JackowskiDepartamento de Psiquiatria & Neuroradiologia, Universidade Federal de São Paulo São Paulo, Brazil.
Venkatesh PanthangiNonhuman Primate Laboratory, Department of Psychiatry and Behavioral Sciences, Downstate Medical Center, State University of New York Brooklyn, NY, USA.
Tarique D PereraGeriatric Psychiatry, New York State Psychiatric Institute New York, NY, USA.
Jack M GormanFranklin Behavioral Health Consultants Bronx, NY, USA.
Yung-Yu HuangDepartment of Molecular Imaging and Neuropathology, New York State Psychiatric Institute New York, NY, USA.
Cheuk Y TangDepartments of Psychiatry, Neuroscience, and Radiology, Icahn School of Medicine at Mount Sinai New York, NY, USA.
Patrick R HofFishberg Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai New York, NY, USA.
Arie KaffmanDepartment of Psychiatry, Yale University School of Medicine New Haven, CT, USA.
Andrew J DworkDepartment of Molecular Imaging and Neuropathology, New York State Psychiatric Institute New York, NY, USA.
Sanjay J MathewMental Health Care Line, Michael E. Debakey VA Medical Center Houston, TX, USA ; Menninger Department of Psychiatry and Behavioral Sciences, Baylor College of Medicine Houston, TX, USA.
Joan KaufmanChild Study Center, Yale University School of Medicine New Haven, CT, USA.
J John MannDepartment of Molecular Imaging and Neuropathology, New York State Psychiatric Institute New York, NY, USA.
New York State Psychiatric InstituteNew York Psychoanalytic Society and Institute · USState University of New York · USYale University · USBaylor College of Medicine · USIcahn School of Medicine at Mount Sinai · USSUNY Downstate Health Sciences University · US

Funding

ADVERSE EARLY REARING &GLUTAMATERGIC FUNCTIONR01MH059990 · NIMH · SUNY DOWNSTATE MEDICAL CENTER · PI COPLAN, JEREMY D · 2000 to 2003
$1.1M
Neural Circuitry of Social Behavior in Bonnet MacaquesR21MH066748 · NIMH · NEW YORK STATE PSYCHIATRIC INSTITUTE · PI GORMAN, JACK M. · 2002 to 2003
$348k
NIMH NIH HHS R01 MH059990NIMH NIH HHS R21 MH066748
6 · The paper itself

Abstract

backgroundEarly life stress (ELS) is cited as a risk for mood and anxiety disorders, potentially through altered serotonin neurotransmission. We examined the effects of ELS, utilizing the variable foraging demand (VFD) macaque model, on adolescent monoamine metabolites. We sought to replicate an increase in cerebrospinal fluid (CSF) 5-hydroxyindoleacetic acid (5-HIAA) observed in two previous VFD cohorts. We hypothesized that elevated cisternal 5-HIAA was associated with reduced neurotrophic effects, conceivably due to excessive negative feedback at somatodendritic 5-HT1A autoreceptors. A putatively decreased serotonin neurotransmission would be reflected by reductions in hippocampal volume and white matter (WM) fractional anisotropy (FA).

methodsWhen infants were 2-6 months of age, bonnet macaque mothers were exposed to VFD. We employed cisternal CSF taps to measure monoamine metabolites in VFD (N = 22) and non-VFD (N = 14) offspring (mean age = 2.61 years). Metabolites were correlated with hippocampal volume obtained by MRI and WM FA by diffusion tensor imaging in young adulthood in 17 males [10 VFD (mean age = 4.57 years)].

resultsVFD subjects exhibited increased CSF 5-HIAA compared to non-VFD controls. An inverse correlation between right hippocampal volume and 5-HIAA was noted in VFD- but not controls. CSF HVA and MHPG correlated inversely with hippocampal volume only in VFD. CSF 5-HIAA correlated inversely with FA of the WM tracts of the anterior limb of the internal capsule (ALIC) only in VFD.

conclusionsElevated cisternal 5-HIAA in VFD may reflect increased dorsal raphe serotonin, potentially inducing excessive autoreceptor activation, inducing a putative serotonin deficit in terminal fields. Resultant reductions in neurotrophic activity are reflected by smaller right hippocampal volume. Convergent evidence of reduced neurotrophic activity in association with high CSF 5-HIAA in VFD was reflected by reduced FA of the ALIC.

Indexed as

cisternal tapmonoamine metabolitesMRIserotonin metabolitevariable foraging demand

Identifiers

PMID25566007
PMCPMC4274982
OpenAlexW1997187863

What OpenQuestion holds

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LicenceCC BY
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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.