Evidence map›Paper›PMID 40344063›Full record

ArticleScience advances2025

Deep compressed multichannel adaptive optics scanning light ophthalmoscope.

Jongwan Park, Kristen Hagan, Theodore B DuBose, Ramiro S Maldonado, Ryan P McNabb, Alfredo Dubra, Joseph A Izatt, Sina Farsiu

Abstract read
In one paragraph

Article in Science advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

8 authors.

Jongwan ParkDepartment of Biomedical Engineering, Duke University, Durham, NC, USA.ORCID 0000-0002-6322-2423
Kristen HaganDepartment of Biomedical Engineering, Duke University, Durham, NC, USA.
Theodore B DuBoseDepartment of Biomedical Engineering, Duke University, Durham, NC, USA.
Ramiro S MaldonadoDepartment of Ophthalmology, Duke University School of Medicine, Durham, NC, USA.ORCID 0000-0002-8440-2095
Ryan P McNabbDepartment of Ophthalmology, Duke University School of Medicine, Durham, NC, USA.ORCID 0000-0002-1686-4191
Alfredo DubraByers Eye Institute, Stanford University, Stanford, CA, USA.ORCID 0000-0002-6506-9020
Joseph A IzattDepartment of Biomedical Engineering, Duke University, Durham, NC, USA.ORCID 0000-0003-1993-2249
Sina FarsiuDepartment of Biomedical Engineering, Duke University, Durham, NC, USA.ORCID 0000-0003-4872-2902

Funding

VISION RESEARCHP30EY005722 · NEI · DUKE UNIVERSITY · PI Vadim Y Arshavsky · 1985 to 2026
$19.3M
Stanford Vision Research CoreP30EY026877 · NEI · STANFORD UNIVERSITY · PI Jeffrey L Goldberg · 2017 to 2026
$8.0M
Increasing the isoplanatic patch in adaptive optics ophthalmoscopyR01EY032147 · NEI · STANFORD UNIVERSITY · PI DUBRA, ALFREDO · 2021 to 2025
$2.4M
Improving rigor and reproducibility in adaptive optics ophthalmoscopyR01EY031360 · NEI · STANFORD UNIVERSITY · PI DUBRA, ALFREDO · 2020 to 2023
$2.3M
Low Latency Eye-Motion CompensationR01EY032669 · NEI · STANFORD UNIVERSITY · PI DUBRA, ALFREDO · 2021 to 2024
$1.8M
NEI NIH HHS P30 EY005722NEI NIH HHS P30 EY026877NEI NIH HHS R01 EY031360NEI NIH HHS R01 EY032147NEI NIH HHS R01 EY032669
6 · The paper itself

Abstract

Adaptive optics scanning light ophthalmoscopy (AOSLO) reveals individual retinal cells and their function, microvasculature, and micropathologies in vivo. As compared to the single-channel offset pinhole and two-channel split-detector nonconfocal AOSLO designs, by providing multidirectional imaging capabilities, a recent generation of multidetector and (multi-)offset aperture AOSLO modalities has been demonstrated to provide critical information about retinal microstructures. However, increasing detection channels requires expensive optical components and/or critically increases imaging time. To address this issue, we present an innovative combination of machine learning and optics as an integrated technology to compressively capture 12 nonconfocal channel AOSLO images simultaneously. Imaging of healthy participants and diseased subjects using the proposed deep compressed multichannel AOSLO showed enhanced visualization of rods, cones, and mural cells with over an order-of-magnitude improvement in imaging speed as compared to conventional offset aperture imaging. To facilitate the adaptation and integration with other in vivo microscopy systems, we made optical design, acquisition, and computational reconstruction codes open source.

Indexed as

OphthalmoscopesOphthalmoscopyHumansImage Processing, Computer-AssistedMachine LearningOptics and PhotonicsRetina

Identifiers

PMID40344063
PMCPMC12063668

What OpenQuestion holds

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LicenceCC BY-NC
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.