# Haemodialysis-Induced Stress Influences Ocular Microcirculation

**Authors:** Joanna Roskal-Wałek, Sylwia Terpiłowska, Joanna Gołębiewska, Jerzy Mackiewicz, Kamila Bołtuć-Dziugieł, Agnieszka Bociek, Paweł Wałek, Michał Biskup, Dominik Odrobina, Andrzej Jaroszyński

PMC · DOI: 10.3390/biomedicines14020454 · Biomedicines · 2026-02-18

## TL;DR

This study shows that a single hemodialysis session affects eye blood flow and tissue thickness, linked to changes in blood markers of stress and endothelial function.

## Contribution

The study is the first to use OCTA to show how hemodialysis impacts retinal and choroidal microcirculation and its relation to biochemical stress markers.

## Key findings

- A single HD session increased retinal thickness and decreased choroidal thickness.
- ET-1 levels increased and ADMA levels decreased after HD, correlating with changes in retinal and choroidal parameters.
- Oxidative stress and osmotic changes were linked to microcirculation and morphological changes in the eye.

## Abstract

Background: Haemodialysis (HD) superimposes additional circulatory stress on the microvasculature, leading to endothelial dysfunction, which plays a key role in the development of haemodialysis-associated multiorgan dysfunction. This study was undertaken to evaluate the effect of a single HD session on retinal and choroidal microcirculation, using optical coherence tomography angiography (OCTA) in relation to changes in the blood levels of selected biochemical modulators of endothelial function. Methods: The vessel density (VD) of 35 patients was evaluated before and after a single HD session, using OCTA in the superficial capillary plexus (SCP), deep capillary plexus (DCP) and choriocapillaris (CC). Retinal thickness (RT) and choroidal thickness (CT) were also assessed. Asymmetric dimethylarginine (ADMA), endothelin-1 (ET-1) and malondialdehyde (MDA) levels, oxidative stress (OS) status and systemic parameters were assessed before and after a single HD session. The correlation between changes in these parameters and changes in selected OCTA parameters was tested. Results: A single HD session resulted in a significant increase in RT and a decrease in CT. In addition to increased oxidative and osmotic stress resulting from a significant reduction in plasma osmolality, the HD session was associated with a significant increase in ET-1 levels and a decrease in ADMA levels. These biochemical changes correlated with changes in RT and CT, as well as with changes in VD in the retinal capillary plexuses and the CC. Increased ET-1 levels and decreased plasma osmolality were identified as predictors of RT increase, whereas increased MDA levels corrected serum creatinine-predicted CT reduction. Conclusions: Changes in ADMA and ET-1 and OS, as well as osmotic stress induced by a single HD session, affect the eye microcirculation and morphology of the retina and choroid. OCTA examination is a promising method for assessing microcirculation in HD patients.

## Linked entities

- **Proteins:** EDN1 (endothelin 1), adma (adrenomedullin a), so (sine oculis)

## Full-text entities

- **Genes:** THAS (thoracoabdominal syndrome) [NCBI Gene 7055] {aka TAS}, AGT (angiotensinogen) [NCBI Gene 183] {aka ANHU, SERPINA8, hFLT1}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, UCN3 (urocortin 3) [NCBI Gene 114131] {aka SCP, SPC, UCNIII}, EDN1 (endothelin 1) [NCBI Gene 1906] {aka ARCND3, ET1, HDLCQ7, PPET1, QME}, ACE (angiotensin I converting enzyme) [NCBI Gene 1636] {aka ACE1, CD143, DCP, DCP1}
- **Diseases:** Vascular dysfunction (MESH:D002561), cardiovascular harm (MESH:D002318), macular oedema (MESH:D008269), infection (MESH:D007239), oedema (MESH:C536897), diabetic retinopathy (MESH:D003930), ESRD (MESH:D007676), atrial fibrillation (MESH:D001281), hypertension (MESH:D006973), epiretinal membrane (MESH:D019773), glomerulonephritis (MESH:D005921), ischaemic insults (MESH:D018917), OS (MESH:D000079225), CT (MESH:D002833), retinal vessel occlusion (MESH:D015356), ocular diseases (MESH:D005128), polycystic kidney disease (MESH:D007690), glaucoma (MESH:D005901), retinal vascular disease (MESH:D012164), microcirculation dysfunction (MESH:D006331), cataract (MESH:D002386), age-related macular degeneration (MESH:D008268), CKD (MESH:D051436), diabetes mellitus (MESH:D003920), retinal pigment epithelium dysfunction (MESH:C536309), acute coronary syndrome (MESH:D054058), pupil dilatation (MESH:D011681), vasculitis (MESH:D014657), injury to (MESH:D014947), ANS (MESH:D001342), macular hole (MESH:D012167), sympathetic hyperactivity (MESH:D006948), uveitis (MESH:D014605), cerebral stroke (MESH:D020521), eye injury (MESH:D005131), multiorgan dysfunction (MESH:D009102)
- **Chemicals:** MDA (MESH:D008315), urea (MESH:D014508), PUFA (MESH:D005231), H2O2 (MESH:D006861), CT (-), ADMA (MESH:C018524), creatinine (MESH:D003404), ROS (MESH:D017382), carbon dioxide (MESH:D002245), tropicamide (MESH:D014331), lipid peroxides (MESH:D008054), oxygen (MESH:D010100), OCT (MESH:C051883), NO (MESH:D009569), water (MESH:D014867)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12938056/full.md

## References

46 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938056/full.md

---
Source: https://tomesphere.com/paper/PMC12938056