Evidence map›Paper›PMID 38862584›Full record

ArticleScientific reports2024

Detection of capillary abnormalities in early diabetic retinopathy using scanning laser ophthalmoscopy and optical coherence tomography combined with adaptive optics.

Marie Elise Wistrup Torm, Michael Pircher, Sophie Bonnin, Jesper Johannesen, Oliver Niels Klefter, Mathias Falck Schmidt, Jette Lautrup Frederiksen, Nicolas Lefaudeux, Jordi Andilla, Claudia Valdes and 7 more

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
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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

17 authors.

Marie Elise Wistrup TormDepartment of Ophthalmology, Center for Research in Eye Diseases, Rigshospitalet, Section 37, Valdemar Hansens Vej 13, 2600, Glostrup, Denmark. mtor0036@regionh.dk.ORCID 0000-0003-1356-5433
Michael PircherCenter for Medical Physics and Biomedical Engineering, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.ORCID 0000-0001-9285-7527
Sophie BonninINSERM-DGOS CIC 1423, CHNO des Quinze-Vingts, 28 Rue de Charenton, 75012, Paris, France.
Jesper JohannesenFaculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 3B, Copenhagen N, Denmark.
Oliver Niels KlefterDepartment of Ophthalmology, Center for Research in Eye Diseases, Rigshospitalet, Section 37, Valdemar Hansens Vej 13, 2600, Glostrup, Denmark.
Mathias Falck SchmidtFaculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 3B, Copenhagen N, Denmark.
Jette Lautrup FrederiksenFaculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 3B, Copenhagen N, Denmark.
Nicolas LefaudeuxImagine Eyes, 18 Rue Charles de Gaulle, Orsay, France.
Jordi AndillaThe Barcelona Institute of Science and Technology, ICFO-Institut de Ciencies Fotoniques, 08860, Castelldefels, Barcelona, Spain.
Claudia ValdesThe Barcelona Institute of Science and Technology, ICFO-Institut de Ciencies Fotoniques, 08860, Castelldefels, Barcelona, Spain.
Pablo Loza-AlvarezThe Barcelona Institute of Science and Technology, ICFO-Institut de Ciencies Fotoniques, 08860, Castelldefels, Barcelona, Spain.ORCID 0000-0002-3129-1213
Luisa Sanchez BreaDepartment of Radiology and Nuclear Medicine, Erasmus Medical Center, Dr. Molewaterplein 40, Rotterdam, The Netherlands.
Danilo Andrade De JesusDepartment of Radiology and Nuclear Medicine, Erasmus Medical Center, Dr. Molewaterplein 40, Rotterdam, The Netherlands.
Kate GrieveINSERM-DGOS CIC 1423, CHNO des Quinze-Vingts, 28 Rue de Charenton, 75012, Paris, France.
Michel PaquesINSERM-DGOS CIC 1423, CHNO des Quinze-Vingts, 28 Rue de Charenton, 75012, Paris, France.
Michael LarsenDepartment of Ophthalmology, Center for Research in Eye Diseases, Rigshospitalet, Section 37, Valdemar Hansens Vej 13, 2600, Glostrup, Denmark.
Kiyoko GochoINSERM-DGOS CIC 1423, CHNO des Quinze-Vingts, 28 Rue de Charenton, 75012, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study tested if a high-resolution, multi-modal, multi-scale retinal imaging instrument can provide novel information about structural abnormalities in vivo. The study examined 11 patients with very mild to moderate non-proliferative diabetic retinopathy (NPDR) and 10 healthy subjects using fundus photography, optical coherence tomography (OCT), OCT angiography (OCTA), adaptive optics scanning laser ophthalmoscopy (AO-SLO), adaptive optics OCT and OCTA (AO-OCT(A)). Of 21 eyes of 11 patients, 11 had very mild NPDR, 8 had mild NPDR, 2 had moderate NPDR, and 1 had no retinopathy. Using AO-SLO, capillary looping, inflections and dilations were detected in 8 patients with very mild or mild NPDR, and microaneurysms containing hyperreflective granular elements were visible in 9 patients with mild or moderate NPDR. Most of the abnormalities were seen to be perfused in the corresponding OCTA scans while a few capillary loops appeared to be occluded or perfused at a non-detectable flow rate, possibly because of hypoperfusion. In one patient with moderate NPDR, non-perfused capillaries, also called ghost vessels, were identified by alignment of corresponding en face AO-OCT and AO-OCTA images. The combination of multiple non-invasive imaging methods could identify prominent microscopic abnormalities in diabetic retinopathy earlier and more detailed than conventional fundus imaging devices.

Indexed as

CapillariesDiabetic RetinopathyOphthalmoscopyTomography, Optical CoherenceAdultAgedFemaleFluorescein AngiographyHumansMaleMiddle AgedRetinal Vessels

Identifiers

PMID38862584
PMCPMC11166634

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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.