Evidence map›Paper›PMID 26074032›Full record

ArticleScientific reports2015

Differential monocular vs. binocular pupil responses from melanopsin-based photoreception in patients with anterior ischemic optic neuropathy.

Chrysanthi Tsika, Sylvain V Crippa, Aki Kawasaki

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.5field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Chromatic Pupillometry in Children.Frontiers in neurology · 2018
    Article
  8. Article
  9. The Pupillary Light Reflex in Idiopathic Intracranial Hypertension.Investigative ophthalmology & visual science · 2016
    Article
  10. 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

3 authors at 2 institutions in 1 country.

Chrysanthi Tsika1] Department of Ophthalmology, University of Lausanne, Hôpital Ophtalmique Jules Gonin and Asile des Aveugles Foundation, Avenue de France 15, Lausanne, Switzerland 1004 [2] Department of Ophthalmology, Medical School of the University of Crete, Greece Eye Clinic, University Hospital of Heraklion, Crete Greece, 71013 Voutes Heraklion Crete, Greece.
Sylvain V CrippaDepartment of Ophthalmology, University of Lausanne, Hôpital Ophtalmique Jules Gonin and Asile des Aveugles Foundation, Avenue de France 15, Lausanne, Switzerland 1004.
Aki KawasakiDepartment of Ophthalmology, University of Lausanne, Hôpital Ophtalmique Jules Gonin and Asile des Aveugles Foundation, Avenue de France 15, Lausanne, Switzerland 1004.
Hôpital Ophtalmique Jules-Gonin · CHUniversity of Lausanne · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We examined the effect of anterior ischemic optic neuropathy (AION) on the activity of intrinsically photosensitive retinal ganglion cells (ipRGCs) using the pupil as proxy. Eighteen patients with AION (10 unilateral, 8 bilateral) and 29 age-matched control subjects underwent chromatic pupillometry. Red and blue light stimuli increasing in 0.5 log steps were presented to each eye independently under conditions of dark and light adaptation. The recorded pupil contraction was plotted against stimulus intensity to generate scotopic and photopic response curves for assessment of synaptically-mediated ipRGC activity. Bright blue light stimuli presented monocularly and binocularly were used for melanopsin activation. The post-stimulus pupil size (PSPS) at the 6th second following stimulus offset was the marker of intrinsic ipRGC activity. Finally, questionnaires were administered to assess the influence of ipRGCs on sleep. The pupil response and PSPS to all monocularly-presented light stimuli were impaired in AION eyes, indicating ipRGC dysfunction. To binocular light stimulation, the PSPS of AION patients was similar to that of controls. There was no difference in the sleep habits of the two groups. Thus after ischemic injury to one or both optic nerves, the summated intrinsic ipRGC activity is preserved when both eyes receive adequate light exposure.

Indexed as

Vision, BinocularVision, MonocularAdultAgedCase-Control StudiesFemaleHumansLightMaleMelanopsinMiddle AgedOptic Neuropathy, IschemicPhotoreceptor CellsPupilRetinal Ganglion CellsRod OpsinsMelanopsinRod Opsins

Identifiers

PMID26074032
PMCPMC4466591
OpenAlexW609684786

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.