Evidence map›Paper›PMID 26192624›Full record

ArticlePloS one2015

FLIMX: A Software Package to Determine and Analyze the Fluorescence Lifetime in Time-Resolved Fluorescence Data from the Human Eye.

Matthias Klemm, Dietrich Schweitzer, Sven Peters, Lydia Sauer, Martin Hammer, Jens Haueisen

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

32 citing papers in PubMed, 52 citations in OpenAlex.

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  7. Real-time open-source FLIM analysis.Frontiers in bioinformatics · 2023
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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.

Matthias KlemmInstitute of Biomedical Engineering and Informatics, Technische Universität Ilmenau, POB 100565, 98694, Ilmenau, Germany.
Dietrich SchweitzerExperimental Ophthalmology, University Hospital Jena, Bachstraße 18, 07740, Jena, Germany.
Sven PetersExperimental Ophthalmology, University Hospital Jena, Bachstraße 18, 07740, Jena, Germany.
Lydia SauerExperimental Ophthalmology, University Hospital Jena, Bachstraße 18, 07740, Jena, Germany.
Martin HammerExperimental Ophthalmology, University Hospital Jena, Bachstraße 18, 07740, Jena, Germany.
Jens HaueisenInstitute of Biomedical Engineering and Informatics, Technische Universität Ilmenau, POB 100565, 98694, Ilmenau, Germany.
Jena University Hospital · DETechnische Universität Ilmenau · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fluorescence lifetime imaging ophthalmoscopy (FLIO) is a new technique for measuring the in vivo autofluorescence intensity decays generated by endogenous fluorophores in the ocular fundus. Here, we present a software package called FLIM eXplorer (FLIMX) for analyzing FLIO data. Specifically, we introduce a new adaptive binning approach as an optimal tradeoff between the spatial resolution and the number of photons required per pixel. We also expand existing decay models (multi-exponential, stretched exponential, spectral global analysis, incomplete decay) to account for the layered structure of the eye and present a method to correct for the influence of the crystalline lens fluorescence on the retina fluorescence. Subsequently, the Holm-Bonferroni method is applied to FLIO measurements to allow for group comparisons between patients and controls on the basis of fluorescence lifetime parameters. The performance of the new approaches was evaluated in five experiments. Specifically, we evaluated static and adaptive binning in a diabetes mellitus patient, we compared the different decay models in a healthy volunteer and performed a group comparison between diabetes patients and controls. An overview of the visualization capabilities and a comparison of static and adaptive binning is shown for a patient with macular hole. FLIMX's applicability to fluorescence lifetime imaging microscopy is shown in the ganglion cell layer of a porcine retina sample, obtained by a laser scanning microscope using two-photon excitation.

Indexed as

FluorescenceSoftwareAdultAgedAnimalsArtifactsDiabetes MellitusEyeFemaleHumansImage Processing, Computer-AssistedMaleMiddle AgedOphthalmoscopyOptical ImagingRetinal Ganglion Cells

Identifiers

PMID26192624
PMCPMC4507995
OpenAlexW1019585819

What OpenQuestion holds

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LicenceCC BY
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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.