Evidence map›Paper›PMID 42401737›Full record

ArticleEye (London, England)2026

Retinal non-perfusion progression in severe non-proliferative and proliferative diabetic retinopathy over time: INSPIRED study report 2.

Wei-Shan Tsai, Sarega Gurudas, Hagar Khalid, Francesca Lamanna, Eleonora Riotto, Taffeta Ching Ning Yamaguchi, Louise Roch, Sobha Sivaprasad

Abstract read
In one paragraph

Article in Eye (London, England), 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

8 authors.

Wei-Shan TsaiNIHR Moorfields Clinical Research Facility and Biomedical Research Centre, Moorfields Eye Hospital NHS Foundation Trust, 162 City Road, London, EC1V 2PD, UK.ORCID http://orcid.org/0000-0001-5945-9316
Sarega GurudasNIHR Moorfields Clinical Research Facility and Biomedical Research Centre, Moorfields Eye Hospital NHS Foundation Trust, 162 City Road, London, EC1V 2PD, UK.
Hagar KhalidNIHR Moorfields Clinical Research Facility and Biomedical Research Centre, Moorfields Eye Hospital NHS Foundation Trust, 162 City Road, London, EC1V 2PD, UK.ORCID http://orcid.org/0000-0002-5311-4015
Francesca LamannaNIHR Moorfields Clinical Research Facility and Biomedical Research Centre, Moorfields Eye Hospital NHS Foundation Trust, 162 City Road, London, EC1V 2PD, UK.ORCID http://orcid.org/0009-0007-7956-6056
Eleonora RiottoNIHR Moorfields Clinical Research Facility and Biomedical Research Centre, Moorfields Eye Hospital NHS Foundation Trust, 162 City Road, London, EC1V 2PD, UK.ORCID http://orcid.org/0000-0002-3593-2516
Taffeta Ching Ning YamaguchiBoehringer Ingelheim International GmbH, Birkendorfer Str. 65, 88397, Biberach, Germany.
Louise RochBoehringer Ingelheim International GmbH, Birkendorfer Str. 65, 88397, Biberach, Germany.
Sobha SivaprasadNIHR Moorfields Clinical Research Facility and Biomedical Research Centre, Moorfields Eye Hospital NHS Foundation Trust, 162 City Road, London, EC1V 2PD, UK. sobha.sivaprasad@nhs.net.

Funding

Boehringer Ingelheim 749092
6 · The paper itself

Abstract

BACKGROUND/

objectivesTo determine the topographic distribution of retinal non-perfusion (RNP) progression in patients with severe non-proliferative diabetic retinopathy (sNPDR) and proliferative diabetic retinopathy (PDR). SUBJECTS/

methodsThis retrospective study was conducted at Moorfields Eye Hospital in the United Kingdom. Patients with diabetic retinopathy (DR) who had two sets of ultra-widefield fundus fluorescein angiography were included. A grid comprising seven concentric rings was superimposed on the images. RNP areas were annotated using Optos' proprietary tool. Total and zonal non-perfusion index (NPI) were calculated as the RNP area divided by the gradable retinal area. Adjusted linear mixed-effects models (LMEMs) were used to estimate progression, accounting for repeated measures and inter-eye correlation.

resultsA total of 53 patients (67 eyes) were included in the analyses. This cohort comprised 19 (28%) eyes with PDR, 31 (46%) with sNPDR, and 17 (25%) with mild-to-moderate NPDR. Focusing on sNPDR and PDR, the nasal 20-30 mm zone had the largest NPI (0.37 ± 0.26) at baseline. Over time, the total NPI increased significantly, with an estimated change of +0.027 (12.42 mm²) per year (95% confidence interval [CI] = 0.008 to 0.045, P = 0.005). The inferior 10-20 mm ring showed the fastest NPI progression ( + 0.049/year; P = 0.007).

conclusionsThis study demonstrates that NPI increased with time in DR. Notably, the inferior 10-20 mm zone was most vulnerable to NPI progression. Of note, this study was limited by the confounding effect of anti-vascular endothelial growth factor (anti-VEGF) treatment; therefore, a future prospective study to control for treatment exposure would be warranted.

Indexed as

Diabetic RetinopathyRetinaAgedDisease ProgressionFemaleFluorescein AngiographyHumansMaleMiddle AgedRetrospective StudiesTomography, Optical CoherenceVisual Acuity

Identifiers

PMID42401737
PMCPMC13601625

What Socratic holds

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Registered trials

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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 Socratic graph.