Evidence map›Paper›PMID 42102314›Full record

ArticleBiomolecules & biomedicine2026

Interocular symmetry in dynamic retinal vessel analysis among healthy adults.

Michael Mendes Wefelnberg, Freerk T Baumann, Henning Guthoff, Damir Zubac

Abstract read
In one paragraph

Article in Biomolecules & biomedicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Michael Mendes WefelnbergDepartment I of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Düsseldorf (CIO ABCD), Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.
Freerk T BaumannDepartment I of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Düsseldorf (CIO ABCD), Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.
Henning GuthoffClinic III for Internal Medicine, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany; Center for Cardiovascular Medicine Aachen Bonn Cologne Düsseldorf (CCM ABCD), Aachen, Bonn, Cologne and Düsseldorf, Germany.
Damir ZubacDepartment I of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Düsseldorf (CIO ABCD), Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dynamic retinal vessel analysis is a non-invasive approach for assessing retinal microvascular endothelial function, yet the extent to which eye selection, interocular variability, and systemic physiological factors influence dynamic retinal vessel analyzer (DRVA)-derived biomarkers remains insufficiently defined. This prospective methodological study aimed to evaluate the interocular symmetry and absolute and relative reliability of arterial flicker-induced dilation (aFID), venular flicker-induced dilation (vFID), and arteriolar constriction (aCON), and to determine whether these parameters are moderated by eye dominance, peak oxygen uptake (V̇O₂ peak), or intraocular pressure (IOP) in healthy individuals. Twenty apparently healthy adults completed two laboratory visits. During the first visit, aerobic capacity was assessed by cardiopulmonary exercise testing until volitional exhaustion. During the second visit, IOP, resting blood pressure, eye dominance, and retinal vascular endothelial function were assessed using DRVA in both eyes in randomized order. Interocular differences were examined using paired comparisons, Bland-Altman analysis, reliability statistics, and linear mixed-effects models accounting for bilateral measurements within participants. No significant differences were observed between the left and right eyes for aFID, vFID, or aCON. Bland-Altman analysis showed no systematic interocular bias across DRVA-derived parameters, although the limits of agreement were widest for aFID, indicating greater interocular variability. Relative reliability was highest for vFID, followed by aCON, whereas aFID showed only fair agreement. Similarly, absolute reliability analyses identified vFID as the most stable biomarker, with the lowest coefficient of variation, while aFID demonstrated the greatest variability. Linear mixed-effects models showed no significant moderating effects of eye dominance, V̇O₂ peak, or IOP on aFID, vFID, or aCON. These findings suggest that retinal vascular endothelial responses measured by DRVA are not systematically influenced by eye dominance or selected systemic physiological factors in healthy young adults. However, given the observed interocular variability, particularly for aFID, assessment of both eyes should be considered in clinical and research settings to improve measurement precision and reproducibility.

Indexed as

Retinal VesselsAdultBlood PressureFemaleHealthy VolunteersHumansIntraocular PressureMaleOxygen ConsumptionReproducibility of ResultsVasodilationYoung Adult

Identifiers

PMID42102314
PMCPMC13394567

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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.