Evidence map›Paper›PMID 28418534›Full record

ArticleJournal of biomedical optics2017

Optical-sectioning microscopy of protoporphyrin IX fluorescence in human gliomas: standardization and quantitative comparison with histology.

Linpeng Wei, Ye Chen, Chengbo Yin, Sabine Borwege, Nader Sanai, Jonathan T C Liu

Open access · goldAbstract readComparative Study
In one paragraph

Article in Journal of biomedical optics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 12% of its field
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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

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  16. Dual-axis confocal microscopy for point-of-care pathology.IEEE journal of selected topics in quantum electronics : a publication of the IEEE Lasers and Electro-optics Society
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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

6 authors at 2 institutions in 1 country.

Linpeng WeiUniversity of Washington, Department of Mechanical Engineering, Seattle, Washington, United States.
Ye ChenUniversity of Washington, Department of Mechanical Engineering, Seattle, Washington, United States.
Chengbo YinUniversity of Washington, Department of Mechanical Engineering, Seattle, Washington, United States.
Sabine BorwegeBarrow Neurological Institute, St. Joseph's Hospital, Phoenix, Arizona, United States.
Nader SanaiBarrow Neurological Institute, St. Joseph's Hospital, Phoenix, Arizona, United States.
Jonathan T C LiuUniversity of Washington, Department of Mechanical Engineering, Seattle, Washington, United States.
University of Washington · USBarrow Neurological Institute · US

Funding

Line-scanned MEMS-based dual-axis confocal microscopy to detect oral lesions in vR01DE023497 · NIDCR · UNIVERSITY OF WASHINGTON · PI LIU, JONATHAN T.C. · 2012 to 2014
$2.4M
Molecular Mechanisms Underlying Glioma Invasion of the Human Subventricular ZoneR01NS082745 · NINDS · ST. JOSEPH'S HOSPITAL AND MEDICAL CENTER · PI SANAI, NADER · 2013 to 2017
$1.8M
Intraoperative confocal microscopy for quantitative delineation of low-grade glioR01CA175391 · NCI · UNIVERSITY OF WASHINGTON · PI LIU, JONATHAN T.C., SANAI, NADER · 2014 to 2018
$1.7M
NCI NIH HHS R01 CA175391NIDCR NIH HHS R01 DE023497NINDS NIH HHS R01 NS082745
6 · The paper itself

Abstract

Systemic delivery of 5-aminolevulinic acid leads to enhanced fluorescence image contrast in many tumors due to the increased accumulation of protoporphyrin IX (PpIX), a fluorescent porphyrin that is associated with tumor burden and proliferation. The value of PpIX-guided resection of malignant gliomas has been demonstrated in prospective randomized clinical studies in which a twofold greater extent of resection and improved progression-free survival have been observed. In low-grade gliomas and at the diffuse infiltrative margins of all gliomas, PpIX fluorescence is often too weak to be detected with current low-resolution surgical microscopes that are used in operating rooms. However, it has been demonstrated that high-resolution optical-sectioning microscopes are capable of detecting the sparse and punctate accumulations of PpIX that are undetectable via conventional low-power surgical fluorescence microscopes. To standardize the performance of high-resolution optical-sectioning devices for future clinical use, we have developed an imaging phantom and methods to ensure that the imaging of PpIX-expressing brain tissues can be performed reproducibly. Ex vivo imaging studies with a dual-axis confocal microscope demonstrate that these methods enable the acquisition of images from unsectioned human brain tissues that quantitatively and consistently correlate with images of histologically processed tissue sections.

Indexed as

Microscopy, FluorescenceOptics and PhotonicsAlgorithmsAminolevulinic AcidBrain NeoplasmsDiagnostic ImagingDisease-Free SurvivalGliomaHumansMicroscopy, ConfocalPhantoms, ImagingProtoporphyrinsSepharoseSignal-To-Noise RatioAminolevulinic Acidprotoporphyrin IXProtoporphyrinsSepharose

Identifiers

PMID28418534
PMCPMC5390779
OpenAlexW2606489488

What OpenQuestion holds

Textmetadata
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.