Evidence map›Paper›PMID 35770824›Full record

ArticleJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2022

Mineral Crystal Thickness in Calcified Cartilage and Subchondral Bone in Healthy and Osteoarthritic Human Knees.

Mikko A J Finnilä, Shuvashis Das Gupta, Mikael J Turunen, Iida Hellberg, Aleksandra Turkiewicz, Viviane Lutz-Bueno, Elin Jonsson, Mirko Holler, Neserin Ali, Velocity Hughes and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

17 citing papers in PubMed, 21 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

16 authors at 6 institutions in 3 countries.

Mikko A J FinniläResearch Unit of Medical Imaging, Physics and Technology, Faculty of Medicine, University of Oulu, Oulu, Finland.ORCID 0000-0002-3348-5759
Shuvashis Das GuptaResearch Unit of Medical Imaging, Physics and Technology, Faculty of Medicine, University of Oulu, Oulu, Finland.ORCID 0000-0001-8905-1231
Mikael J TurunenDepartment of Applied Physics, Faculty of Science and Forestry, University of Eastern Finland, Kuopio, Finland.ORCID 0000-0003-1093-1178
Iida HellbergResearch Unit of Medical Imaging, Physics and Technology, Faculty of Medicine, University of Oulu, Oulu, Finland.ORCID 0000-0003-2824-9310
Aleksandra TurkiewiczClinical Epidemiology Unit, Orthopaedics, Department of Clinical Sciences Lund, Faculty of Medicine, Lund University, Lund, Sweden.ORCID 0000-0003-1460-2275
Viviane Lutz-BuenoPaul Scherrer Institut, Villigen PSI, Switzerland.ORCID 0000-0001-9735-5470
Elin JonssonClinical Epidemiology Unit, Orthopaedics, Department of Clinical Sciences Lund, Faculty of Medicine, Lund University, Lund, Sweden.ORCID 0000-0002-6119-5804
Mirko HollerPaul Scherrer Institut, Villigen PSI, Switzerland.ORCID 0000-0001-8141-0148
Neserin AliClinical Epidemiology Unit, Orthopaedics, Department of Clinical Sciences Lund, Faculty of Medicine, Lund University, Lund, Sweden.
Velocity HughesClinical Epidemiology Unit, Orthopaedics, Department of Clinical Sciences Lund, Faculty of Medicine, Lund University, Lund, Sweden.ORCID 0000-0002-3869-7726
Hanna IsakssonDepartment of Biomedical Engineering, Lund University, Lund, Sweden.ORCID 0000-0002-9690-8907
Jon TjörnstrandDepartment of Orthopaedics, Skåne University Hospital, Lund, Sweden.ORCID 0000-0002-2100-8074
Patrik ÖnnerfjordRheumatology and Molecular Skeletal Biology, Department of Clinical Sciences Lund, Faculty of Medicine, Lund University, Lund, Sweden.ORCID 0000-0002-2345-2937
Manuel Guizar-SicairosPaul Scherrer Institut, Villigen PSI, Switzerland.ORCID 0000-0002-8293-3634
Simo SaarakkalaResearch Unit of Medical Imaging, Physics and Technology, Faculty of Medicine, University of Oulu, Oulu, Finland.ORCID 0000-0003-2850-5484
Martin EnglundClinical Epidemiology Unit, Orthopaedics, Department of Clinical Sciences Lund, Faculty of Medicine, Lund University, Lund, Sweden.ORCID 0000-0003-3320-2437
Lund University · SEPaul Scherrer Institute · CHUniversity of Oulu · FIOulu University Hospital · FISkåne University Hospital · SEUniversity of Eastern Finland · FI

Funding

Academy of Finland 268378Academy of Finland 303786Finnish Cultural Foundation and The North Ostrobothnia Regional Fund 60172246Forskningsrådet om Hälsa, Arbetsliv och VälfärdGovernmental funding of clinical research within the national health servicesH2020 European Research Council 336267H2020 Marie Skłodowska-Curie Actions 713645Österlund FoundationSwedish Research Council 2019-00953Swedish Research Council 2020-01103The Finnish Foundation for Technology PromotionThe Swedish Rheumatology Association
6 · The paper itself

Abstract

Osteoarthritis (OA) is the most common joint disease, where articular cartilage degradation is often accompanied with sclerosis of the subchondral bone. However, the association between OA and tissue mineralization at the nanostructural level is currently not understood. In particular, it is technically challenging to study calcified cartilage, where relevant but poorly understood pathological processes such as tidemark multiplication and advancement occur. Here, we used state-of-the-art microfocus small-angle X-ray scattering with a 5-μm spatial resolution to determine the size and organization of the mineral crystals at the nanostructural level in human subchondral bone and calcified cartilage. Specimens with a wide spectrum of OA severities were acquired from both medial and lateral compartments of medial compartment knee OA patients (n = 15) and cadaver knees (n = 10). Opposing the common notion, we found that calcified cartilage has thicker and more mutually aligned mineral crystals than adjoining bone. In addition, we, for the first time, identified a well-defined layer of calcified cartilage associated with pathological tidemark multiplication, containing 0.32 nm thicker crystals compared to the rest of calcified cartilage. Finally, we found 0.2 nm thicker mineral crystals in both tissues of the lateral compartment in OA compared with healthy knees, indicating a loading-related disease process because the lateral compartment is typically less loaded in medial compartment knee OA. In summary, we report novel changes in mineral crystal thickness during OA. Our data suggest that unloading in the knee might be involved with the growth of mineral crystals, which is especially evident in the calcified cartilage. © 2022 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).

Indexed as

Cartilage, ArticularOsteoarthritisOsteoarthritis, KneeBone and BonesHumansKnee JointMineralsMineralsANALYSIS/QUANTITATION OF BONEBONE MODELING AND REMODELINGCOLLAGENMATRIX MINERALIZATIONOSTEOARTHRITIS

Identifiers

PMID35770824
PMCPMC9540032
OpenAlexW4283742894

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.