Evidence map›Paper›PMID 41356305›Full record

ReviewReviews in cardiovascular medicine2025

Biomarkers and Mechanisms of Cardiovascular Susceptibility and Resilience to Post-Traumatic Stress Disorder.

Eugenia B Manukhina, Maryrita K Mallet, Vadim E Tseilikman, Marina V Kondashevskaya, Olga P Budanova, H Fred Downey, Robert T Mallet

Abstract readReview
In one paragraph

Review in Reviews in cardiovascular medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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.

Eugenia B ManukhinaLaboratory for Regulatory Mechanisms of Stress and Adaptation, Institute of General Pathology and Pathophysiology, 125315 Moscow, Russia.ORCID https://orcid.org/0000-0002-8102-173X
Maryrita K MalletDepartment of Physiology and Anatomy, University of North Texas Health Science Center, Fort Worth, TX 76107, USA.ORCID https://orcid.org/0009-0006-9381-7926
Vadim E TseilikmanSchool of Basic Medicine, Chelyabinsk State University, 454001 Chelyabinsk, Russia.ORCID https://orcid.org/0000-0003-2935-7487
Marina V KondashevskayaLaboratory of Cell Pathology, Avtsyn Research Institute of Human Morphology of the Petrovsky National Research Center of Surgery, 117418 Moscow, Russia.ORCID https://orcid.org/0000-0002-8096-5974
Olga P BudanovaLaboratory for Regulatory Mechanisms of Stress and Adaptation, Institute of General Pathology and Pathophysiology, 125315 Moscow, Russia.ORCID https://orcid.org/0000-0002-6650-5082
H Fred DowneyDepartment of Physiology and Anatomy, University of North Texas Health Science Center, Fort Worth, TX 76107, USA.ORCID https://orcid.org/0000-0002-7280-1021
Robert T MalletDepartment of Physiology and Anatomy, University of North Texas Health Science Center, Fort Worth, TX 76107, USA.ORCID https://orcid.org/0000-0001-7388-9419

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Post-traumatic stress disorder (PTSD), which develops in susceptible individuals after life-threatening or traumatizing events, manifests as a heightened anxiety and startle reflex, disordered sleep, nightmares, flashbacks, and avoidance of triggers. Moreover, PTSD is a predictor and independent risk factor of numerous cardiovascular comorbidities, including stroke, myocardial infarction, coronary atherosclerosis, and atrial fibrillation. Compounding the direct detrimental effects of PTSD on the cardiovascular system, this condition provokes classical cardiovascular risk factors, including high cholesterol and triglycerides, platelet hyperaggregation, endothelial dysfunction, hypertension, and sympathetic hyperactivation. Although most people who have experienced traumatic events do not develop PTSD and are considered PTSD resilient, a substantial minority experience persistent cardiovascular comorbidities. Experimental and clinical studies have revealed a myriad of biomarkers and/or mediators of PTSD susceptibility and resilience, including pro- and anti-inflammatory cytokines, oxidized proteins and lipids, antioxidants, troponin, catecholamines and their metabolites, glucocorticoids, and pro-coagulation factors. The use of biomarkers to predict cardiovascular susceptibility or resilience to PTSD may stratify the risk of a patient developing cardiovascular complications following severe stress. Indeed, since many PTSD biomarkers either inflict or attenuate cardiovascular damage, these biomarkers can be applied to monitor the efficacy of exercise, dietary modifications, and other interventions to enhance cardiovascular resilience and, thereby, restrict the detrimental effects of PTSD on the cardiovascular system. Biomarker-informed therapy is a promising strategy to minimize the risk and impact of cardiovascular diseases in individuals with PTSD.

Indexed as

biomarkerscardiovascular systemcatecholaminescytokinesglucocorticoidsinflammationmyocardial injuryoxidative stresspost-traumatic stress disorderpsychotherapy

Identifiers

PMID41356305
PMCPMC12681009

What Socratic 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 Socratic graph.