Evidence map›Paper›PMID 41244990›Full record

ArticleOphthalmology science2026

Using the Rate of Global and Pointwise Microperimetry Change to Predict Structural Conversion in Intermediate Age-Related Macular Degeneration.

Jeremy C K Tan, Giovanni Montesano, Charlotte Behning, Hannah M P Dunbar, Robert P Finger, Adnan Tufail, Jan H Terheyden, Frank G Holz, Ulrich F O Luhmann, David P Crabb and 1 more

Registry-linked trialAbstract 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. It is linked to trial NCT03349801 (Development of Novel Clinical Endpoints for Interventional Clinical Trials With a Regulatory and Patient Access Intention in Patients With Intermediate Age-related Macular Degeneration), which is not on this map. Not yet cited in PubMed.

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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.

NCT03349801 active not recruitingnot on this map

Development of Novel Clinical Endpoints for Interventional Clinical Trials With a Regulatory and Patient Access Intention in Patients With Intermediate Age-related Macular Degeneration (AMD)

TypeobservationalSponsorFrank G. HolzRan2018 to 2026Enrolled718ConditionsAge Related Macular Degeneration (AMD)ArmsNo intervention
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

11 authors.

Jeremy C K TanOptometry and Visual Sciences, City St George's, University of London, London, UK.
Giovanni MontesanoOptometry and Visual Sciences, City St George's, University of London, London, UK.
Charlotte BehningInstitute of Medical Biometry, Informatics and Epidemiology, Medical Faculty, University of Bonn, Bonn, Germany.
Hannah M P DunbarMoorfields Eye Hospital NHS Foundation Trust, London, UK.
Robert P FingerDepartment of Ophthalmology, Mannheim University Hospital, Mannheim, Germany.
Adnan TufailMoorfields Eye Hospital NHS Foundation Trust, London, UK.
Jan H TerheydenOptometry and Visual Sciences, City St George's, University of London, London, UK.
Frank G HolzDepartment of Ophthalmology, University Hospital Bonn, Bonn, Germany.
Ulrich F O LuhmannRoche Pharmaceutical Research and Early Development, Translational Medicine Ophthalmology, Roche Innovation Center Basel, Basel, Switzerland.
David P CrabbOptometry and Visual Sciences, City St George's, University of London, London, UK.
MACUSTAR Consortium

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Studies evaluating functional change in age-related macular degeneration (AMD) using microperimetry often measure the difference in global mean sensitivity at interval time points versus baseline. We evaluate the rate of global and pointwise microperimetry change in intermediate AMD (iAMD) in the multicenter MACUSTAR (Registration NCT03349801) study and assess their prognostic value in structural conversion to late-stage AMD. Design: Prospective study. Subjects: Four hundred forty-seven subjects with iAMD (Beckman classification) from 20 European sites. Methods: Subjects that underwent mesopic microperimetry on ≥3 follow-up visits were included. Two methods of assessing functional progression were evaluated: (1) global mean sensitivity regression and (2) pointwise sensitivity regression at fastest progressing N number of locations (N from 1 to 10). Rates of microperimetry progression were then evaluated in an initial series of visits prior to structural conversion to late-stage AMD. Main Outcome Measures: Area under the receiving operating characteristic (AUC) curves and Cox proportional hazard models were used to assess risk of structural conversion based on rate of functional progression. Results: The mean age of subjects was 72 (standard deviation 7) years. The median number of visits and duration of follow-up was 6 visits and 3 years, respectively. Structural conversion to late-stage AMD was observed in 80 (17.9%) eyes. In the visits prior to conversion, there was a greater rate of global mean sensitivity loss in eyes that eventually developed late-stage AMD compared with those that did not (-1.05 vs. -0.30 decibels/year, Conclusions: In the analysis of longitudinal microperimetry data from the MACUSTAR study, the rate of global and pointwise sensitivity change was significantly greater and strongly prognostic of eyes that developed structural conversion. Our findings support use of these trend-based pointwise analysis methods in assessing functional progression in iAMD. Financial Disclosures: Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.

Indexed as

Intermediate age-related macular degenerationMacustarMicroperimetryVisual field

Identifiers

PMID41244990
PMCPMC12613102

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Registered trials

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.