Evidence map›Paper›PMID 36928369›Full record

ArticleScientific reports2023

Adapted clustering method for generic analysis of histological fibrosis staining as an open source tool.

Anca Remes, Marie Noormalal, Nesrin Schmiedel, Norbert Frey, Derk Frank, Oliver J Müller, Markus Graf

Open access · goldFull text read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

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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

7 authors at 4 institutions in 1 country.

Anca RemesDepartment of Internal Medicine III, University Hospital Schleswig-Holstein, Kiel and German Centre for Cardiovascular Research, Partner Site Hamburg/Kiel/Lübeck, Kiel, Germany.
Marie NoormalalDepartment of Internal Medicine III, University Hospital Schleswig-Holstein, Kiel and German Centre for Cardiovascular Research, Partner Site Hamburg/Kiel/Lübeck, Kiel, Germany.
Nesrin SchmiedelDepartment of Internal Medicine III, University Hospital Schleswig-Holstein, Kiel and German Centre for Cardiovascular Research, Partner Site Hamburg/Kiel/Lübeck, Kiel, Germany.
Norbert FreyDepartment of Internal Medicine III, University Hospital Heidelberg, Heidelberg, Germany.
Derk FrankDepartment of Internal Medicine III, University Hospital Schleswig-Holstein, Kiel and German Centre for Cardiovascular Research, Partner Site Hamburg/Kiel/Lübeck, Kiel, Germany.
Oliver J MüllerDepartment of Internal Medicine III, University Hospital Schleswig-Holstein, Kiel and German Centre for Cardiovascular Research, Partner Site Hamburg/Kiel/Lübeck, Kiel, Germany.
Markus GrafFaculty Industrial and Process Engineering, Heilbronn University of Applied Sciences, Heilbronn, Max-Planck-Str. 39, 74081, Heilbronn, Germany. markus.graf@hs-heilbronn.de.
German Centre for Cardiovascular Research · DEUniversity of Lübeck · DEHeilbronn University · DEUniversity Hospital Heidelberg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pathological remodeling of the extracellular matrix is a hallmark of cardiovascular disease. Abnormal fibrosis causes cardiac dysfunction by reducing ejection fraction and impairing electrical conductance, leading to arrhythmias. Hence, accurate quantification of fibrosis deposition in histological sections is of extreme importance for preclinical and clinical studies. Current automatic tools do not perform well under variant conditions. Moreover, users do not have the option to evaluate data from staining methods of their choice according to their purpose. To overcome these challenges, we underline a novel machine learning-based tool (FibroSoft) and we show its feasibility in a model of cardiac hypertrophy and heart failure in mice. Our results demonstrate that FibroSoft can identify fibrosis in diseased myocardium and the obtained results are user-independent. In addition, the results acquired using our software strongly correlate to those obtained by Western blot analysis of collagen 1 expression. Additionally, we could show that this method can be used for Masson's Trichrome and Picosirius Red stained histological images. The evaluation of our method also indicates that it can be used for any particular histology segmentation and quantification. In conclusion, our approach provides a powerful example of the feasibility of machine learning strategies to enable automatic analysis of histological images.

Indexed as

Heart FailureMyocardiumAnimalsCluster AnalysisFibrosisMiceStaining and Labeling

Identifiers

PMID36928369
PMCPMC10020481
OpenAlexW4327573023

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Textfull text, public
LicenceCC BY
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Registered trials

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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.