Evidence map›Paper›PMID 40194960›Full record

ArticleBiology of the cell2025

Undergrowth Collagen Fibers Analysis by Fingerprint Enhancement Method.

Clara Manesco, Thierry Cloitre, Marta Martin, Yannick Nicolas Gerber, Florence Evelyne Perrin, Oscar Saavedra-Villanueva, Csilla Gergely

Abstract read
In one paragraph

Article in Biology of the cell, 2025. 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

7 authors.

Clara ManescoLaboratoire Charles Coulomb (L2C), Université de Montpellier, CNRS, Montpellier, France.
Thierry CloitreLaboratoire Charles Coulomb (L2C), Université de Montpellier, CNRS, Montpellier, France.
Marta MartinLaboratoire Charles Coulomb (L2C), Université de Montpellier, CNRS, Montpellier, France.
Yannick Nicolas GerberMMDN, Université de Montpellier, INSERM, Montpellier, France.
Florence Evelyne PerrinLaboratoire Charles Coulomb (L2C), Université de Montpellier, CNRS, Montpellier, France.
Oscar Saavedra-VillanuevaLaboratoire Charles Coulomb (L2C), Université de Montpellier, CNRS, Montpellier, France.
Csilla GergelyLaboratoire Charles Coulomb (L2C), Université de Montpellier, CNRS, Montpellier, France.

Funding

ANR (the French National Research Agency) under the "Investissements d'avenir" program ANR-16-IDEX-0006
6 · The paper itself

Abstract

Collagen is a key protein in mammals that maintains structural integrity within tissues. A failure in fibrillar collagen reorganization can induce cancer or fibrosis formation, such as in spinal cord injury (SCI), where the healing process after the initial trauma leads to the formation of scar tissue, which includes fibrosis. As there is no current treatment targeting the fibrotic process directly, a better understanding of collagen properties can thus help to apprehend malignant states. Characterization of collagen fibers has been widely explored on second-harmonic generation (SHG) images, due to the label-free nature of the SHG imaging technique. It has been performed with various fibers extraction methods such as curvelet transform (CT) implemented in the open-source software CurveAlign. However, when it comes to investigating undergrowth collagen fibers (collagen fibers that are still under reorganization) as observed in SCI, the CT method becomes complex to tune for nonadvanced users in order to properly segment the fibers. To improve collagen detection in the case of undergrowth fibers, we propose a methodology based on the fingerprint enhancement (FP-E) algorithm that requires fewer user input parameters and is less time-consuming. Our method was extensively tested on SHG data from injured spinal cord samples. We obtained metrics that depicted changes in collagen organization over time, particularly a significant increase in fiber density, demonstrating the FP-E algorithm was properly adapted to address the evolution of collagen properties after SCI. Besides the simpler tuning of the method compared to commonly used software, the combination with further characterization of the extracted fibers could lead to consider fibrillar collagen as a biomarker in diseases where fibers are under development. The FP-E algorithm is provided in the article.

Indexed as

CollagenImage Processing, Computer-AssistedSpinal Cord InjuriesAlgorithmsAnimalsHumansSoftwareCollagencollagenfibril characterizationimage processingsecond‐harmonic generation (SHG)segmentation

Identifiers

PMID40194960
PMCPMC11975548

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.