# Interplay of anxiety, depression, vascular function, and biomarkers in post-myocardial infarction patients

**Authors:** Jan Kafol, Borut Jug, Mojca Božič Mijovski, Jure Tršan, Daniel Košuta, Marko Novaković

PMC · DOI: 10.3389/fphys.2025.1594889 · Frontiers in Physiology · 2025-05-26

## TL;DR

The study finds that anxiety and depression in heart attack patients are linked to vascular issues and specific blood markers, suggesting mental health assessments should be part of heart care.

## Contribution

The study identifies novel associations between anxiety/depression and vascular function/biomarkers in post-MI patients.

## Key findings

- Anxiety is significantly associated with younger age, higher BMI, and increased arterial stiffness.
- Fibrinogen levels are higher in participants with anxiety and depression, while endocan and BDNF levels are lower in those with anxiety.

## Abstract

Coronary artery disease (CAD) is a leading cause of mortality. Depression and anxiety are common in CAD patients and negatively affect quality of life, physical functioning, and adherence to cardiac rehabilitation (CR) programs. This study aimed to identify possible associations with clinically relevant parameters, vascular function and blood biomarkers.

Participants were consecutively recruited during cardiac rehabilitation intake visits at the University Medical Centre Ljubljana within 4 months of myocardial infarction (MI). Hospital Anxiety and Depression Scale (HADS) scores were analyzed in relation to endothelial function (assessed with flow-mediated dilation), arterial stiffness, and blood biomarkers (fibrinogen, endocan, and brain-derived neurotrophic factor [BDNF]) in post-MI patients. All vascular and biomarker assessments were performed within 5 days of questionnaire completion and prior to the start of rehabilitation.

There were 105 patients included in the study. The median age was 56 years (49–62), and 80.0% of participants were male. Clinically relevant anxiety and depression were present in 29.5% and 21.9% of participants, respectively. Anxiety was significantly associated with younger age, higher body mass index, and increased arterial stiffness, with total HADS scores negatively correlated with age. Endothelial function showed no significant associations with HADS scores. Vital signs showed no significant differences, except for slightly higher systolic blood pressure in those with clinically relevant depression. Fibrinogen levels were significantly higher in participants with anxiety and depression, while endocan and BDNF levels were lower in those with anxiety.

Depression and especially anxiety are significantly associated with endothelial function and relevant biomarkers in post-MI patients. However, as HADS is a screening tool and not a diagnostic instrument, and given the study’s observational design, findings reflect associations rather than causality. Routine screening and targeted mental health support within CR programs might improve participation, enhance cardiovascular recovery, and optimize long-term outcomes. These findings underscore the clinical importance of psychological assessment in the early post-MI period and support the integration of mental health evaluation into cardiovascular care.

## Linked entities

- **Proteins:** BDNF (brain derived neurotrophic factor)
- **Diseases:** coronary artery disease (MONDO:0005010), myocardial infarction (MONDO:0005068), anxiety (MONDO:0005618), depression (MONDO:0002050)

## Full-text entities

- **Genes:** BDNF (brain derived neurotrophic factor) [NCBI Gene 627] {aka ANON2, BULN2}, FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}, ESM1 (endothelial cell specific molecule 1) [NCBI Gene 11082] {aka endocan}
- **Diseases:** Anxiety (MESH:D001007), MI (MESH:D009203), Depression (MESH:D003866), CAD (MESH:D003324)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12146154/full.md

## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC12146154/full.md

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Source: https://tomesphere.com/paper/PMC12146154