Evidence map›Paper›PMID 36607619›Full record

ArticleInvestigative ophthalmology & visual science2023

Microperimetry and Adaptive Optics Imaging Reveal Localized Functional and Structural Changes in Asymptomatic RPGR Mutation Carriers.

Danial Roshandel, Tina M Lamey, Jason Charng, Rachael C Heath Jeffery, Terri L McLaren, Jennifer A Thompson, John N De Roach, Samuel McLenachan, David A Mackey, Fred K Chen

Open access · goldAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Retinitis pigmentosa GTPase regulator-related retinopathy and gene therapy.Saudi journal of ophthalmology : official journal of the Saudi Ophthalmological Society
    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 4 institutions in 1 country.

Danial RoshandelCentre for Ophthalmology and Visual Science, The University of Western Australia, Nedlands, Western Australia, Australia.
Tina M LameyCentre for Ophthalmology and Visual Science, The University of Western Australia, Nedlands, Western Australia, Australia.
Jason CharngCentre for Ophthalmology and Visual Science, The University of Western Australia, Nedlands, Western Australia, Australia.
Rachael C Heath JefferyCentre for Ophthalmology and Visual Science, The University of Western Australia, Nedlands, Western Australia, Australia.
Terri L McLarenCentre for Ophthalmology and Visual Science, The University of Western Australia, Nedlands, Western Australia, Australia.
Jennifer A ThompsonAustralian Inherited Retinal Disease Registry and DNA Bank, Department of Medical Technology and Physics, Sir Charles Gairdner Hospital, Nedlands, Western Australia, Australia.
John N De RoachCentre for Ophthalmology and Visual Science, The University of Western Australia, Nedlands, Western Australia, Australia.
Samuel McLenachanCentre for Ophthalmology and Visual Science, The University of Western Australia, Nedlands, Western Australia, Australia.
David A MackeyCentre for Ophthalmology and Visual Science, The University of Western Australia, Nedlands, Western Australia, Australia.
Fred K ChenCentre for Ophthalmology and Visual Science, The University of Western Australia, Nedlands, Western Australia, Australia.
Sir Charles Gairdner Hospital · AUUniversity of Western Australia · AULions Eye Institute · AUCentre for Eye Research Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Female carriers of RPGR mutations demonstrate no significant retinal dysfunction or structural change despite a characteristic tapetal-like reflex. In this study, we examined localized changes of pointwise sensitivity (PWS) and cone density (CD) using microperimetry (MP) and adaptive optics (AO) imaging in female carriers of RPGR mutations. Methods: In this cross-sectional case-control study, MP (MAIA, 10-2 test grid) and AO imaging (rtx1) were performed in female carriers of RPGR mutations and unrelated age-matched healthy controls. PWS at 68 loci located 1 degree to 9 degrees away from the preferred retinal locus and CD at 12 loci located 1 degree to 3 degrees away from the foveal center were measured. Severity of defect was defined by standard deviation (SD) from age-matched healthy control means: normal (<1 SD from normal average), moderate defect (1-2 SD from normal average), and severe defect (>2 SD from normal average). Results: Twelve patients from seven unrelated families were enrolled. Seven patients were asymptomatic, 5 of whom had visual acuity 20/20 or better in both eyes. PWS and CD were available in 12 and 8 patients, respectively. Severe PWS and CD defect in at least 1 test location was observed in 10 of 12 patients and 7 of 8 patients, respectively. Among the five asymptomatic patients who had normal visual acuity, severe PWS and CD defects were observed in three of five and four of five patients, respectively. Conclusions: MP and AO imaging revealed early functional and structural changes in asymptomatic RPGR mutation carriers and should be considered in clinical assessment of these patients.

Indexed as

Tomography, Optical CoherenceVisual Field TestsCase-Control StudiesCross-Sectional StudiesEye ProteinsFemaleHumansMutationEye ProteinsRPGR protein, human

Identifiers

PMID36607619
PMCPMC9836009
OpenAlexW4313650006

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.