Evidence map›Paper›PMID 27506655›Full record

ArticleBehavioural brain research2016

The role of genes involved in stress, neural plasticity, and brain circuitry in depressive phenotypes: Convergent findings in a mouse model of neglect.

Janitza L Montalvo-Ortiz, Kelly A Bordner, Becky C Carlyle, Joel Gelernter, Arthur A Simen, Joan Kaufman

Abstract read
In one paragraph

Article in Behavioural brain research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

17 citing papers in PubMed, 35 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.

Janitza L Montalvo-OrtizDepartment of Psychiatry, Yale University, New Haven, CT, 06520, United States.
Kelly A BordnerSouthern Connecticut State University, New Haven, CT, United States.
Becky C CarlyleDepartment of Psychiatry, Yale University, New Haven, CT, 06520, United States.
Joel GelernterDepartment of Psychiatry, Yale University, New Haven, CT, 06520, United States; Veterans Administration, West Haven, CT, United States.
Arthur A SimenNeuroscience Research Unit, Pfizer Worldwide Research & Development, Cambridge, MA, United States.
Joan KaufmanCenter for Child and Family Traumatic Stress, Kennedy Krieger Institute, United States; Department of Psychiatry, Johns Hopkins School of Medicine, United States. Electronic address: joan.kaufman@kennedykrieger.org.
Yale University · USKennedy Krieger Institute · USPfizer (United States) · USSouthern Connecticut State University · USUnited States Department of Veterans Affairs · US

Funding

Institutional Career Development CoreKL2TR001862 · NCATS · YALE UNIVERSITY · PI CANTLEY, LLOYD G, EDELMAN, E. JENNIFER · 2016 to 2025
$12.2M
RESEARCH TRAINING - BIOLOGICAL SCIENCEST32MH014276 · NIMH · YALE UNIVERSITY · PI Marina R Picciotto · 1985 to 2026
$7.2M
Risk and Resilience in Maltreated ChildrenR01MH098073 · NIMH · YALE UNIVERSITY · PI HUDZIAK, JAMES J., KAUFMAN, JOAN R. · 2012 to 2015
$3.0M
Genetic and Environmental Modifiers of Child DepressionR01MH077087 · NIMH · YALE UNIVERSITY · PI KAUFMAN, JOAN R. · 2006 to 2009
$1.5M
NCATS NIH HHS KL2 TR001862NIMH NIH HHS R01 MH077087NIMH NIH HHS R01 MH098073NIMH NIH HHS T32 MH014276
6 · The paper itself

Abstract

Early life neglect increases risk for the development of psychopathologies during childhood and adulthood, including depression and anxiety disorders. We recently reported epigenetic changes in DNA derived from saliva in three genes predicted depression in a cohort of maltreated children: DNA-binding protein inhibitor ID-3 (ID3), Glutamate NMDA Receptor (GRIN1), and Tubulin Polymerization Promoting Protein (TPPP). To validate the role of these genes in depression risk, secondary analyses were conducted of gene expression data obtained from medial prefrontal cortex (mPFC) tissue of mice subjected to a model of maternal neglect which included maternal separation and early weaning (MSEW). Anxiety and depression-like phenotype data derived using the elevated plus maze (EPM) and forced swimming test (FST), respectively, were also available for secondary analyses. Behavioral tests were conducted in MSEW and control adult male mice when they were between 65 and 80days old. ID3, GRIN1 and TPPP gene expression in the mPFC were found to significantly predict behavioral differences in the EPM and FST. These results further support the role of these genes in the etiology of depressive and anxiety phenotypes following early life stress.

Indexed as

Maternal DeprivationAnimalsDepressionDisease Models, AnimalGene Expression RegulationInhibitor of Differentiation ProteinsMaleMaze LearningMiceMice, Inbred C57BLMice, Inbred DBAMicroarray AnalysisNerve Tissue ProteinsNeuronal PlasticityPrefrontal CortexReceptors, N-Methyl-D-AspartateGprin1 protein, mouseIdb3 protein, mouseInhibitor of Differentiation ProteinsNerve Tissue ProteinsReceptors, N-Methyl-D-AspartateRNA, MessengerTPPP protein, mouseDepressionDNA-binding protein inhibitor ID-3 (ID3)Glutamate NMDA receptor (GRIN1)MethylationNeglectTubulin polymerization promoting protein (TPPP)

Identifiers

PMID27506655
PMCPMC5396458
OpenAlexW2487954867

What OpenQuestion holds

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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.