Evidence map›Paper›PMID 33345061›Full record

ArticleFrontiers in sports and active living2020

Achilles Subtendon Structure and Behavior as Evidenced From Tendon Imaging and Computational Modeling.

Geoffrey G Handsfield, Joachim Greiner, Josef Madl, Eva A Rog-Zielinska, Enzo Hollville, Benedicte Vanwanseele, Vickie Shim

Open access · goldAbstract read
In one paragraph

Article in Frontiers in sports and active living, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 30 citations in OpenAlex.

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  11. 3D characterization of the triple-bundle Achilles tendon from in vivo high-field MRI.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 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

7 authors at 3 institutions in 3 countries.

Geoffrey G HandsfieldAuckland Bioengineering Institute, University of Auckland, Auckland, New Zealand.
Joachim GreinerInstitute for Experimental Cardiovascular Medicine, University Heart Center Freiburg Bad Krozingen, Bad Krozingen, Germany.
Josef MadlInstitute for Experimental Cardiovascular Medicine, University Heart Center Freiburg Bad Krozingen, Bad Krozingen, Germany.
Eva A Rog-ZielinskaInstitute for Experimental Cardiovascular Medicine, University Heart Center Freiburg Bad Krozingen, Bad Krozingen, Germany.
Enzo HollvilleHuman Movement Biomechanics Research Group, Department of Movement Sciences, KU Leuven, Leuven, Belgium.
Benedicte VanwanseeleHuman Movement Biomechanics Research Group, Department of Movement Sciences, KU Leuven, Leuven, Belgium.
Vickie ShimAuckland Bioengineering Institute, University of Auckland, Auckland, New Zealand.
University of Freiburg · DEKU Leuven · BEUniversity of Auckland · NZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Achilles tendon is the largest and strongest tendon in the human body and is essential for storing elastic energy and positioning the foot for walking and running. Recent research into Achilles tendon anatomy and mechanics has revealed the importance of the Achilles subtendons, which are unique and semi-independent structures arising from each of the three muscular heads of the triceps surae. Of particular importance is the ability for the subtendons to slide, the role that this has in healthy tendons, and the alteration of this property in aging and disease. In this work, we discuss technical approaches that have led to the current understanding of Achilles subtendons, particularly imaging and computational modeling. We introduce a 3D geometrical model of the Achilles subtendons, built from dual-echo UTE MRI. We revisit and discuss computational models of Achilles subtendon twisting suggesting that optimal twist reduces both rupture loads and stress concentrations by distributing stresses. Second harmonic generation imaging shows collagenous subtendons within a rabbit Achilles tendon; a clear absence of signal between the subtendons indicates an inter-subtendon region on the order of 30 μm in our rabbit animal model. Entry of wheat germ agglutinin in both the inter-fascicular and the inter-subtendon regions suggests a glycoprotein-containing inter-subtendon matrix which may facilitate low friction sliding of the subtendons in healthy mammals. Lastly, we present a new computational model coupled with human exercise trials to demonstrate the magnitude of Achilles subtendon sliding which occurs during rehabilitation exercises for Achilles tendinopathy, and shows that specific exercise can maximize subtendon sliding and interface strains, without maximizing subtendon strains. This work demonstrates the value of imaging and computational modeling for probing tendon structure-function relationships and may serve to inform and develop treatments for Achilles tendinopathy.

Indexed as

biomechanicsfinite elementfunctionMRIsecond harmonic

Identifiers

PMID33345061
PMCPMC7739789
OpenAlexW3037608240

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.