Evidence map›Paper›PMID 41970585›Full record

ArticleBiomedical optics express2026

Functional OCT with parfocal retinal stimulation enables multi-site optoretinography under a single dark adaptation.

Amit Hasan Sadhin, Taeyoon Son, Shaiban Ahmed, Guangying Ma, Masrur Arefin Sadhin, Xincheng Yao

Abstract read
In one paragraph

Article in Biomedical optics express, 2026. 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

6 authors.

Amit Hasan SadhinDepartment of Biomedical Engineering, University of Illinois Chicago, Chicago, IL 60607, USA.ORCID https://orcid.org/0000-0003-1600-3022
Taeyoon SonDepartment of Biomedical Engineering, University of Illinois Chicago, Chicago, IL 60607, USA.
Shaiban AhmedDepartment of Biomedical Engineering, University of Illinois Chicago, Chicago, IL 60607, USA.ORCID https://orcid.org/0009-0003-5284-6964
Guangying MaDepartment of Biomedical Engineering, University of Illinois Chicago, Chicago, IL 60607, USA.ORCID https://orcid.org/0000-0002-7990-1420
Masrur Arefin SadhinDepartment of Biomedical Engineering, University of Illinois Chicago, Chicago, IL 60607, USA.ORCID https://orcid.org/0009-0003-0430-7229
Xincheng YaoDepartment of Biomedical Engineering, University of Illinois Chicago, Chicago, IL 60607, USA.ORCID https://orcid.org/0000-0002-0356-3242

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Functional optical coherence tomography (OCT) enables depth-resolved imaging of stimulus-evoked intrinsic optical signal (IOS) changes in the retina, providing a noninvasive method for objective optoretinography (ORG) of retinal physiology. However, IOS imaging with raster-scan OCT is limited by long acquisition times, as each recording site typically requires a separate dark-adaptation cycle. To overcome this constraint, we developed a functional OCT system with parfocal retinal stimulation, in which the visible-light stimulus and near-infrared OCT imaging beams are co-registered at the retina. This configuration confines stimulation to a local retinal region with high spatial precision, preserves dark adaptation elsewhere, and enables multi-site IOS acquisition within a single adaptation cycle. Using visible-light flashes with variable bleaching levels (1-100%), we observed robust, spatially localized IOS confined to the stimulated regions of the retina. The IOS amplitude scaled linearly with bleaching level up to approximately 20% and exhibited saturation at higher intensities, consistent with the biophysical limits of phototransduction. This parfocal stimulation strategy establishes a scalable framework for spatially and depth-resolved functional retinal mapping, providing an objective optical analogue to microperimetry and a foundation for site-specific assessment of photoreceptor physiology.

Identifiers

PMID41970585
PMCPMC13064622

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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.