Evidence map›Paper›PMID 38393604›Full record

ReviewMolecular biology reports2024

Prominent genetic variants and epigenetic changes in post-traumatic stress disorder among combat veterans.

Ahmadali Baghaei, Mojtaba Yousefi Zoshk, Mohsen Hosseini, Hossein Fasihi, Ehsan Nassireslami, Sevda Shayesteh, Reza Laripour, Aynaz Eslami Amoli, Reza Heidari, Mohsen Chamanara

Abstract readReview
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In one paragraph

Review in Molecular biology reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. 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

10 authors at 3 institutions in 1 country.

Ahmadali BaghaeiTrauma Research center, AJA university of Medical sciences, Tehran, Iran.
Mojtaba Yousefi ZoshkTrauma Research center, AJA university of Medical sciences, Tehran, Iran.
Mohsen HosseiniThe Institute of Pharmaceutical Sciences (TIPS), Tehran University of Medical Sciences, Tehran, Iran.
Hossein FasihiBiomaterial and Medicinal Chemistry Research Center, AJA University of Medical Science, Tehran, Iran.
Ehsan NassireslamiToxicology Research Center, AJA University of Medical Sciences, Tehran, Iran.
Sevda ShayestehDepartment of Pharmacology and Toxicology, Faculty of Pharmacy, Alborz University of Medical Sciences, Karaj, Iran.
Reza LaripourSocial and Preventive Medicine Department, School of Medicine, AJA University of Medical Sciences, Tehran, Iran.
Aynaz Eslami AmoliTrauma Research center, AJA university of Medical sciences, Tehran, Iran.
Reza HeidariCancer Epidemiology Research Center (AJA-CERTC), AJA University of Medical Sciences, Tehran, Iran. r-Heidary@ajaums.ac.ir.
Mohsen ChamanaraToxicology Research Center, AJA University of Medical Sciences, Tehran, Iran. chamanaramohsen@gmail.com.
Aja University of Medical Sciences · IRJahrom University of Medical Sciences · IRTehran University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Post-traumatic stress disorder (PTSD) is one of the most widespread and disabling psychiatric disorders among combat veterans. Substantial interindividual variability in susceptibility to PTSD suggests the presence of different risk factors for this disorder. Twin and family studies confirm genetic factors as important risk factors for PTSD. In addition to genetic factors, epigenetic factors, especially DNA methylation, can be considered as a potential mechanism in changing the risk of PTSD. So far, many genetic and epigenetic association studies have been conducted in relation to PTSD. In genetic studies, many single nucleotide polymorphisms have been identified as PTSD risk factors. Meanwhile, the variations in catecholamines-related genes, serotonin transporter and receptors, brain-derived neurotrophic factor, inflammatory factors, and apolipoprotein E are the most prominent candidates. CpG methylation in the upstream regions of many genes is also considered a PTSD risk factor. Accurate identification of genetic and epigenetic changes associated with PTSD can lead to the presentation of suitable biomarkers for susceptible individuals to this disorder. This study aimed to delineate prominent genetic variations and epigenetic changes associated with post-traumatic stress disorder in military veterans who have experienced combat, focusing on genetic and epigenetic association studies.

Indexed as

Stress Disorders, Post-TraumaticVeteransDNA MethylationEpigenesis, GeneticHumansPolymorphism, Single NucleotideDNA methylationEpigeneticGenetic polymorphismPost-traumatic stress disorder

Identifiers

PMID38393604
OpenAlexW4392122175

What OpenQuestion holds

Textmetadata
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.