Evidence map›Paper›PMID 25206954›Full record

ArticleEuropean journal of psychotraumatology2014

Biomarkers for combat-related PTSD: focus on molecular networks from high-dimensional data.

Thomas C Neylan, Eric E Schadt, Rachel Yehuda

Open access · goldAbstract read
In one paragraph

Article in European journal of psychotraumatology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

14 citing papers in PubMed, 25 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

3 authors at 2 institutions in 1 country.

Thomas C NeylanDepartment of Psychiatry, University of California, San Francisco, CA, USA ; Mental Health Service, San Francisco Veterans Affairs Medical Center, San Francisco, CA, USA.
Eric E SchadtDepartment of Genetics and Genomic Sciences, Mount Sinai School of Medicine, New York, NY, USA.
Rachel YehudaDepartment of Psychiatry, James J. Peters Veterans Affairs Medical Center, Bronx, NY, USA ; Department of Psychiatry and Neurobiology, Mount Sinai School of Medicine, New York, NY, USA.
Icahn School of Medicine at Mount Sinai · USSan Francisco VA Medical Center · US

Funding

Integrative Network Biology Approaches to Identify, Characterize and Validate Molecular Subtypes in Alzheimer's DiseaseU01AG046170 · NIA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI WANG, MINGHUI, ZHANG, BIN · 2013 to 2022
$26.0M
1/3-Networks from Multidimensional Data for Schizophrenia and Related DisordersR01MH097276 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI SCHADT, ERIC E, SKLAR, PAMELA · 2012 to 2014
$2.5M
Neuroendocrine Regulation of Sleep in PTSDR01MH073978 · NIMH · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI NEYLAN, THOMAS C · 2005 to 2008
$1.8M
Cognitive Behavioral Treatment of Insomnia in Posttraumatic Stress DisorderR34MH077667 · NIMH · NORTHERN CALIFORNIA INSTITUTE/RES/EDU · PI NEYLAN, THOMAS C · 2008 to 2010
$638k
NIA NIH HHS U01 AG046170NIMH NIH HHS R01 MH073978NIMH NIH HHS R01 MH097276NIMH NIH HHS R34 MH077667
6 · The paper itself

Abstract

Posttraumatic stress disorder (PTSD) and other deployment-related outcomes originate from a complex interplay between constellations of changes in DNA, environmental traumatic exposures, and other biological risk factors. These factors affect not only individual genes or bio-molecules but also the entire biological networks that in turn increase or decrease the risk of illness or affect illness severity. This review focuses on recent developments in the field of systems biology which use multidimensional data to discover biological networks affected by combat exposure and post-deployment disease states. By integrating large-scale, high-dimensional molecular, physiological, clinical, and behavioral data, the molecular networks that directly respond to perturbations that can lead to PTSD can be identified and causally associated with PTSD, providing a path to identify key drivers. Reprogrammed neural progenitor cells from fibroblasts from PTSD patients could be established as an in vitro assay for high throughput screening of approved drugs to determine which drugs reverse the abnormal expression of the pathogenic biomarkers or neuronal properties.

Indexed as

Computational Biologygene expressiongenomicsproteomicsPTSDrisk factors

Identifiers

PMID25206954
PMCPMC4138711
OpenAlexW1994083855

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.