Evidence map›Paper›PMID 32296985›Full record

ArticleJournal of bone and mineral metabolism2020

The old sheep: a convenient and suitable model for senile osteopenia.

Stefan Maenz, Olaf Brinkmann, Ines Hasenbein, Christina Braun, Elke Kunisch, Victoria Horbert, Francesca Gunnella, André Sachse, Sabine Bischoff, Harald Schubert and 5 more

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of bone and mineral metabolism, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 27% 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

7 citing papers in PubMed, 8 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

15 authors at 4 institutions in 1 country.

Stefan Maenz *Chair of Materials Science, Otto Schott Institute of Materials Research, Friedrich-Schiller-University Jena, Jena, Germany.
Olaf Brinkmann *Chair of Orthopedics, Department of Orthopedics, Jena University Hospital, Waldkliniken Eisenberg GmbH, Eisenberg, Germany.
Ines HasenbeinExperimental Rheumatology Unit, Department of Orthopedics, Jena University Hospital, Waldkliniken Eisenberg GmbH, Klosterlausnitzer Str. 81, 07607, Eisenberg, Germany.
Christina BraunExperimental Rheumatology Unit, Department of Orthopedics, Jena University Hospital, Waldkliniken Eisenberg GmbH, Klosterlausnitzer Str. 81, 07607, Eisenberg, Germany.
Elke KunischExperimental Rheumatology Unit, Department of Orthopedics, Jena University Hospital, Waldkliniken Eisenberg GmbH, Klosterlausnitzer Str. 81, 07607, Eisenberg, Germany.
Victoria HorbertExperimental Rheumatology Unit, Department of Orthopedics, Jena University Hospital, Waldkliniken Eisenberg GmbH, Klosterlausnitzer Str. 81, 07607, Eisenberg, Germany.
Francesca GunnellaExperimental Rheumatology Unit, Department of Orthopedics, Jena University Hospital, Waldkliniken Eisenberg GmbH, Klosterlausnitzer Str. 81, 07607, Eisenberg, Germany.
André SachseExperimental Rheumatology Unit, Department of Orthopedics, Jena University Hospital, Waldkliniken Eisenberg GmbH, Klosterlausnitzer Str. 81, 07607, Eisenberg, Germany.
Sabine BischoffInstitute of Laboratory Animal Sciences and Welfare, Jena University Hospital, Jena, Germany.
Harald SchubertInstitute of Laboratory Animal Sciences and Welfare, Jena University Hospital, Jena, Germany.
Klaus D JandtChair of Materials Science, Otto Schott Institute of Materials Research, Friedrich-Schiller-University Jena, Jena, Germany.
Jörg BossertChair of Materials Science, Otto Schott Institute of Materials Research, Friedrich-Schiller-University Jena, Jena, Germany.
Dominik DrieschBioControl Jena GmbH, Jena, Germany.
Raimund W Kinne *Experimental Rheumatology Unit, Department of Orthopedics, Jena University Hospital, Waldkliniken Eisenberg GmbH, Klosterlausnitzer Str. 81, 07607, Eisenberg, Germany. raimund.w.kinne@med.uni-jena.de.
Matthias Bungartz *Chair of Orthopedics, Department of Orthopedics, Jena University Hospital, Waldkliniken Eisenberg GmbH, Eisenberg, Germany.
Waldkrankenhaus Rudolf Elle · DEJena University Hospital · DESchott (Germany) · DEFriedrich Schiller University Jena · DE

Funding

Bundesministerium für Bildung und Forschung FKZ 0316205BBundesministerium für Bildung und Forschung FKZ 0316205CBundesministerium für Bildung und Forschung FKZ 035577DBundesministerium für Bildung und Forschung FKZ 13N12601Carl-Zeiss-Stiftung doctoral candidate scholarship
6 · The paper itself

Abstract

introductionExisting osteoporosis models in sheep exhibit some disadvantages, e.g., challenging surgical procedures, serious ethical concerns, failure of reliable induction of substantial bone loss, or lack of comparability to the human condition. This study aimed to compare bone morphological and mechanical properties of old and young sheep, and to evaluate the suitability of the old sheep as a model for senile osteopenia. MATERIALS AND

methodsThe lumbar vertebral body L3 of female merino sheep with two age ranges, i.e., old animals (6-10 years; n = 41) and young animals (2-4 years; n = 40), was analyzed concerning its morphological and mechanical properties by bone densitometry, quantitative histomorphometry, and biomechanical testing of the corticalis and/or central spongious region.

resultsIn comparison with young sheep, old animals showed only marginally diminished bone mineral density of the vertebral bodies, but significantly decreased structural (bone volume, - 15.1%; ventral cortical thickness, - 11.8%; lateral cortical thickness, - 12.2%) and bone formation parameters (osteoid volume, osteoid surface, osteoid thickness, osteoblast surface, all - 100.0%), as well as significantly increased bone erosion (eroded surface, osteoclast surface). This resulted in numerically decreased biomechanical properties (compressive strength; - 6.4%).

conclusionOld sheep may represent a suitable model of senile osteopenia with markedly diminished bone structure and formation, and substantially augmented bone erosion. The underlying physiological aging concept reduces challenging surgical procedures and ethical concerns and, due to complex alteration of different facets of bone turnover, may be well representative of the human condition.

Indexed as

Disease Models, AnimalAnimalsBiomechanical PhenomenaBone DensityBone Diseases, MetabolicCancellous BoneCompressive StrengthElastic ModulusFemaleLumbar VertebraeOsteogenesisSheepLarge animal modelOld sheepSenile osteopeniaSenile osteoporosis

Identifiers

PMID32296985
OpenAlexW3017236617

What OpenQuestion holds

Textmetadata
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.