Evidence map›Paper›PMID 41717236›Full record

ArticleOphthalmology science2026

Visual Field Estimation in X-Linked Retinitis Pigmentosa Associated with Retinitis Pigmentosa GTPase Regulator (

Malena Daich Varela, William Woof, Yathusha Kumarasamy, Matthias Monhart, Lynn Kandakji, Gunjan Naik, Pallavi Bagga, Alan Wilter Sousa, Dun Jack Fu, Catey Bunce and 3 more

Abstract read
In one paragraph

Article in Ophthalmology science, 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
–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

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

13 authors.

Malena Daich VarelaMoorfields Eye Hospital, London, United Kingdom.
William WoofUCL Institute of Ophthalmology, University College London, London, United Kingdom.
Yathusha KumarasamyMoorfields Eye Hospital, London, United Kingdom.
Matthias MonhartHaag-Streit AG, Bern, Switzerland.
Lynn KandakjiUCL Institute of Ophthalmology, University College London, London, United Kingdom.
Gunjan NaikUCL Institute of Ophthalmology, University College London, London, United Kingdom.
Pallavi BaggaUCL Institute of Ophthalmology, University College London, London, United Kingdom.
Alan Wilter SousaUCL Institute of Ophthalmology, University College London, London, United Kingdom.
Dun Jack FuMoorfields Eye Hospital, London, United Kingdom.
Catey BunceLondon School of Hygiene and Tropical Medicine, London, United Kingdom.
Konstantinos BalaskasMoorfields Eye Hospital, London, United Kingdom.
Nikolas PontikosMoorfields Eye Hospital, London, United Kingdom.
Michel MichaelidesMoorfields Eye Hospital, London, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: To develop an efficient approach to estimating visual field (VF) in patients with X-linked retinitis pigmentosa (RP) based on macular OCT scans. Design: Retrospective analysis of patients who were enrolled in a natural history study at Moorfields Eye Hospital (London, United Kingdom). Subjects: Male patients with genetically confirmed retinitis pigmentosa GTPase regulator ( Methods: Visual field raw data were exported and analyzed including Visual Field Modeling and Analysis software. Retinal imaging consisted of OCT macular scans. Paired imaging and VF data acquired within a 1-month range were jointly analyzed. Artificial intelligence (AI) was used to automatically segment and quantify macular ellipsoid zone width (EZW), and ellipsoid zone area (EZA). Main Outcome Measures: Functional parameters from static VF testing such as mean sensitivity (MS) and Hill of Vision analysis that included total volume (V Results: Patient age ranged from 5 to 55 years old at baseline. A total of 332 OCT-VF pairs were analyzed. Ellipsoid zone area had the highest conditional R Conclusions: This study showed that AI enables efficient acquiring of large amounts of structural OCT parameters, facilitating research and structure-function predictions. The cohort included patients with a wide range of disease severity and statistical significance was achieved with parameters representing a wide range of VF, proving that this method can be applied for patients with milder disease. Financial Disclosures: Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.

Indexed as

AIGeneticsRetinaRetinitis pigmentosaVisual field

Identifiers

PMID41717236
PMCPMC12914202

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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.