Evidence map›Paper›PMID 40700079›Full record

ArticleVision (Basel, Switzerland)2025

Uncovering the Characteristics of Pupil Cycle Time (PCT) in Neuropathies and Retinopathies.

Laure Trinquet, Suzon Ajasse, Frédéric Chavane, Richard Legras, Frédéric Matonti, José-Alain Sahel, Catherine Vignal-Clermont, Jean Lorenceau

Abstract read
In one paragraph

Article in Vision (Basel, Switzerland), 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. 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

8 authors.

Laure TrinquetFaculté des Sciences Médicales et Paramédicales, Aix-Marseille Université, 13385 Marseille, France.
Suzon AjasseInstitut de la Vision, Sorbonne Université, INSERM, CNRS, 75252 Paris, France.
Frédéric ChavaneInstitut des Neurosciences de la Timone-CNRS UMR 7289, 13005 Marseille, France.
Richard LegrasLuMIn, CNRS, ENS Paris-Saclay, Centrale Supelec, Université Paris-Saclay, 91190 Orsay, France.ORCID 0000-0002-1430-3649
Frédéric MatontiCentre Monticelli Paradis d'Ophtalmologie, 13008 Marseille, France.ORCID 0000-0002-6180-3937
José-Alain SahelDepartment of Ophthalmology, University of Pittsburgh, Pittsburgh, PA 15219, USA.
Catherine Vignal-ClermontHopital Fondation, Adolphe de Rothschild 29, Rue Manin, 75019 Paris, France.ORCID 0000-0003-0292-8905
Jean LorenceauIntegrative Neuroscience and Cognition Center, UMR8002, Université Paris Cité, 75006 Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pupil cycle time (PCT) estimates the dynamics of a biofeedback loop established between pupil size and stimulus luminance, size or colour. The PCT is useful for probing the functional integrity of the retinopupillary circuits, and is therefore potentially applicable for assessing the effects of damage due to retinopathies or neuropathies. In previous studies, PCT was measured by manually counting the number of pupil oscillations during a fixed period to calculate the PCT. This method is scarce, requires a good expertise and cannot be used to estimate several PCT parameters, such as the oscillation amplitude or variability. We have developed a computerised setup based on eye-tracking that expands the possibilities of characterising PCT along several dimensions: oscillation frequency and regularity, amplitude and variability, which can be used with a large palette of stimuli (different colours, sizes, shapes or locations), and further allows measuring blinking frequency and eye movements. We used this method to characterise the PCT in young control participants as well as in patients with several pathologies, including age-related macular degeneration (AMD), diabetic retinopathy (DR), retinitis pigmentosa (RP), Stargardt disease (SD), and Leber hereditary optic neuropathy (LHON). We found that PCT is very regular and stable in young healthy participants, with little inter-individual variability. In contrast, several PCT features are altered in older healthy participants as well as in ocular diseases, including slower dynamics, irregular oscillations, and reduced oscillation amplitude. The distinction between patients and healthy participants based on the calculation of the area under the curve of the receiver operating characteristics (AUC of ROC) were dependent on the pathologies and stimuli (0.7 < AUC < 1). PCT nevertheless provides relevant complementary information to assess the physiopathology of ocular diseases and to probe the functioning of retino-pupillary circuits.

Indexed as

diseasesoscillationpupilretina

Identifiers

PMID40700079
PMCPMC12286252

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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.