Evidence map›Paper›PMID 36645454›Full record

ArticleGraefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie2023

Central retina plays a decisive role in the suppression of pupillary escape.

Carina Kelbsch, Ricarda Jendritza, Torsten Strasser, Felix Tonagel, Paul Richter, Ronja Jung, Tobias Peters, Helmut Wilhelm, Barbara Wilhelm, Krunoslav Stingl

Open access · hybridAbstract read
In one paragraph

Article in Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 38% of its field
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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

10 authors at 2 institutions in 1 country.

Carina KelbschUniversity Eye Hospital, Centre for Ophthalmology, University of Tuebingen, Tübingen, Germany.
Ricarda JendritzaPupil Research Group at the Centre for Ophthalmology, University of Tuebingen, Elfriede-Aulhorn-Straße 7, 72076, Tübingen, Germany.
Torsten StrasserUniversity Eye Hospital, Centre for Ophthalmology, University of Tuebingen, Tübingen, Germany.
Felix TonagelUniversity Eye Hospital, Centre for Ophthalmology, University of Tuebingen, Tübingen, Germany.
Paul RichterUniversity Eye Hospital, Centre for Ophthalmology, University of Tuebingen, Tübingen, Germany.
Ronja JungUniversity Eye Hospital, Centre for Ophthalmology, University of Tuebingen, Tübingen, Germany.
Tobias PetersPupil Research Group at the Centre for Ophthalmology, University of Tuebingen, Elfriede-Aulhorn-Straße 7, 72076, Tübingen, Germany.
Helmut WilhelmUniversity Eye Hospital, Centre for Ophthalmology, University of Tuebingen, Tübingen, Germany.
Barbara WilhelmPupil Research Group at the Centre for Ophthalmology, University of Tuebingen, Elfriede-Aulhorn-Straße 7, 72076, Tübingen, Germany. Barbara.wilhelm@stz-eyetrial.de.
Krunoslav StinglUniversity Eye Hospital, Centre for Ophthalmology, University of Tuebingen, Tübingen, Germany.
University of Tübingen · DESTZ eyetrial · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo explore the pupil redilation during persistent light exposure (pupillary escape phenomenon) at the macula and periphery with monochromatic light stimuli.

methodsForty healthy subjects aged 18-64 years (24 females) were examined by chromatic pupil campimetry (CPC) using red and blue 4-s stimuli of 10° radius at the center and 20°-peripheral locations one per quadrant. One glaucoma patient and one achromatopsia patient served as disease models. For statistical analyses, linear mixed-effects models were performed followed by post hoc t-tests.

resultsA distinct pupillary escape could be demonstrated peripherally (blue 0.099%*s, red 0.153%*s); at the central healthy retina, there was no relevant escape, neither for blue nor red stimulation. Comparing central versus peripheral stimulation revealed highly significant differences in the escape (difference blue 0.100 ± 0.013, red 0.144 ± 0.013, < 0.0001, respectively). In the periphery, the escape was significantly more pronounced for red compared with blue stimulation (difference 0.054 ± 0.013; p = 0.0001). Enhanced pupillary escape outside of the 95% confidence interval of the linear mixed-effects model of the healthy population could be exemplarily shown in a patient with glaucomatous ganglion cell damage. In the achromatopsia example, no relevant escape was found for blue stimulation, but for red stimulation in the periphery in a comparable range to healthy controls.

conclusionThe results emphasize that an intact inner retinal network of nerve fibers arising from the central macular region is necessary for maintaining pupillary constriction during a bright 4-s light stimulus and preventing increase of pupillary escape. Increasing receptive field sizes towards the periphery on the level of retinal ganglion cells and less input from central 1:1 connections could be one of the driving mechanisms for pupillary escape.

Indexed as

Color Vision DefectsGlaucomaFemaleHumansLightPhotic StimulationPupilReflex, PupillaryRetinaCentral retinaChromatic pupil campimetryPeripheral retinaPupil behaviorPupillary escapePupil light reflex

Identifiers

PMID36645454
PMCPMC10199107
OpenAlexW4316371974

What OpenQuestion 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 OpenQuestion graph.