Evidence map›Paper›PMID 38948152›Full record

ArticleNpj imaging2024

Deep learning-based virtual H& E staining from label-free autofluorescence lifetime images.

Qiang Wang, Ahsan R Akram, David A Dorward, Sophie Talas, Basil Monks, Chee Thum, James R Hopgood, Malihe Javidi, Marta Vallejo

Abstract read
In one paragraph

Article in Npj imaging, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

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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

9 authors.

Qiang WangCentre for Inflammation Research, Institute of Regeneration and Repair, The University of Edinburgh, Edinburgh, UK.
Ahsan R AkramCentre for Inflammation Research, Institute of Regeneration and Repair, The University of Edinburgh, Edinburgh, UK.
David A DorwardCentre for Inflammation Research, Institute of Regeneration and Repair, The University of Edinburgh, Edinburgh, UK.
Sophie TalasCentre for Inflammation Research, Institute of Regeneration and Repair, The University of Edinburgh, Edinburgh, UK.
Basil MonksDepartment of Pathology, Royal Infirmary of Edinburgh, Edinburgh, UK.
Chee ThumDepartment of Pathology, Royal Infirmary of Edinburgh, Edinburgh, UK.
James R HopgoodSchool of Engineering, The University of Edinburgh, Edinburgh, UK.
Malihe JavidiSchool of Mathematical and Computer Sciences, Heriot-Watt University, Edinburgh, UK.
Marta VallejoSchool of Mathematical and Computer Sciences, Heriot-Watt University, Edinburgh, UK.

Funding

Wellcome Trust
6 · The paper itself

Abstract

Label-free autofluorescence lifetime is a unique feature of the inherent fluorescence signals emitted by natural fluorophores in biological samples. Fluorescence lifetime imaging microscopy (FLIM) can capture these signals enabling comprehensive analyses of biological samples. Despite the fundamental importance and wide application of FLIM in biomedical and clinical sciences, existing methods for analysing FLIM images often struggle to provide rapid and precise interpretations without reliable references, such as histology images, which are usually unavailable alongside FLIM images. To address this issue, we propose a deep learning (DL)-based approach for generating virtual Hematoxylin and Eosin (H&E) staining. By combining an advanced DL model with a contemporary image quality metric, we can generate clinical-grade virtual H&E-stained images from label-free FLIM images acquired on unstained tissue samples. Our experiments also show that the inclusion of lifetime information, an extra dimension beyond intensity, results in more accurate reconstructions of virtual staining when compared to using intensity-only images. This advancement allows for the instant and accurate interpretation of FLIM images at the cellular level without the complexities associated with co-registering FLIM and histology images. Consequently, we are able to identify distinct lifetime signatures of seven different cell types commonly found in the tumour microenvironment, opening up new opportunities towards biomarker-free tissue histology using FLIM across multiple cancer types.

Indexed as

Cancer imagingEngineering

Identifiers

PMID38948152
PMCPMC11213708

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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.