Evidence map›Paper›PMID 41867243›Full record

ArticleFrontiers in physiology2026

3D imaging and anisotropy mapping of the lamb disc for biomechanical and regenerative insights.

Ana Prates Soares, Andreia Sousa da Silveira, Jussi-Petteri Suuronen, Paul Helmerking, Timm Weitkamp, Bernhard Hesse, Katharina Schmidt-Bleek, Carsten Rendenbach

Abstract read
In one paragraph

Article in Frontiers in physiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Ana Prates SoaresJulius Wolff Institute for Biomechanics and Musculoskeletal Regeneration, Berlin Institute of Health at Charité - Universitätsmedizin Berlin, Berlin, Germany.
Andreia Sousa da SilveiraDepartment for Operative, Preventive and Pediatric Dentistry - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.
Jussi-Petteri SuuronenXploraytion GmbH, Berlin, Germany.
Paul HelmerkingXploraytion GmbH, Berlin, Germany.
Timm WeitkampSynchrotron SOLEIL, Saint-Aubin, France.
Bernhard HesseXploraytion GmbH, Berlin, Germany.
Katharina Schmidt-BleekJulius Wolff Institute for Biomechanics and Musculoskeletal Regeneration, Berlin Institute of Health at Charité - Universitätsmedizin Berlin, Berlin, Germany.
Carsten RendenbachJulius Wolff Institute for Biomechanics and Musculoskeletal Regeneration, Berlin Institute of Health at Charité - Universitätsmedizin Berlin, Berlin, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The temporomandibular joint (TMJ) relies on a fibrocartilaginous disc for stabilization and load distribution. When the disc degenerates, current replacement options fail to restore native biomechanics. Developing effective implants requires detailed knowledge of the disc's structure. The present work provides a full-volume, three-dimensional characterization of collagen fiber architecture and anisotropy in a large animal model with anatomical and functional similarities to the human joint. Methods: A multimodal 3D imaging workflow was implemented, combining cone-beam CT for anatomical context and synchrotron phase-contrast micro-CT for high-resolution visualization of the ovine temporomandibular joint disc, cartilage, ligament, and subchondral bone. Deep-learning segmentation enabled full-volume tissue segmentation. Fiber orientation and anisotropy were quantified using mean intercept length (Mean Intercept Length)-derived eigenvector fields, with analysis performed across anatomical axes and planes. Histological sections validated fiber segmentation and regional differences in extracellular matrix organization. Results: The lamb TMJ disc displayed a heterogeneous but highly ordered collagen network. Strong lateromedial alignment formed frontal-plane reinforcement bands, while a craniocaudal tensile corridor dominated the sagittal plane, and mixed lateromedial-ventrodorsal orientations characterized the transverse plane. Anisotropy was highest in the peripheral rims and lower in the central zone, reflecting a functional division between stabilization and deformation. Quantitative analysis demonstrated an orthotropic organization, with distinct dominant fiber populations aligned along the lateral-medial, ventral-dorsal, and cranial-caudal axes. Subchondral bone beneath the disc exhibited a fine, highly anisotropic trabecular lattice with reduced spacing, complementing the disc's structural organization. Conclusion: This study provides the first full-volume, plane-resolved 3D description of collagen anisotropy in the ovine TMJ disc. The orthotropic fiber architecture and regional anisotropy gradients identified here clarify direction-dependent mechanical behavior and offer quantitative benchmarks for the design of biomimetic scaffolds and regenerative TMJ disc replacements.

Indexed as

anisotropybiomechanicsfibrocartilagemicrotomographysynchrotron radiationtemporomandibular joint (TMJ)

Identifiers

PMID41867243
PMCPMC12999453

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.