Evidence map›Paper›PMID 31590365›Full record

ArticleJournal of clinical medicine2019

Divergent Mononuclear Cell Participation and Cytokine Release Profiles Define Hip and Knee Osteoarthritis.

Ricardo Grieshaber-Bouyer, Till Kämmerer, Nils Rosshirt, Timo A Nees, Philipp Koniezke, Elena Tripel, Marcus Schiltenwolf, Johannes Kirsch, Sébastien Hagmann, Babak Moradi

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 30 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

10 authors at 2 institutions in 2 countries.

Ricardo Grieshaber-BouyerUniversity Clinic of Heidelberg, Clinic for Orthopaedic and Trauma Surgery, Schlierbacher, Landstr, 200a 69118 Heidelberg, Germany. Ricardo.GrieshaberBouyer@med.uni-heidelberg.de.
Till KämmererUniversity Clinic of Heidelberg, Clinic for Orthopaedic and Trauma Surgery, Schlierbacher, Landstr, 200a 69118 Heidelberg, Germany. Till.Kaemmerer@med.uni-heidelberg.de.
Nils RosshirtUniversity Clinic of Heidelberg, Clinic for Orthopaedic and Trauma Surgery, Schlierbacher, Landstr, 200a 69118 Heidelberg, Germany. Nils.Rosshirt@med.uni-heidelberg.de.
Timo A NeesUniversity Clinic of Heidelberg, Clinic for Orthopaedic and Trauma Surgery, Schlierbacher, Landstr, 200a 69118 Heidelberg, Germany. Timo.Nees@med.uni-heidelberg.de.
Philipp KoniezkeUniversity Clinic of Heidelberg, Clinic for Orthopaedic and Trauma Surgery, Schlierbacher, Landstr, 200a 69118 Heidelberg, Germany. Philipp.Koniezke@med.uni-heidelberg.de.
Elena TripelUniversity Clinic of Heidelberg, Clinic for Orthopaedic and Trauma Surgery, Schlierbacher, Landstr, 200a 69118 Heidelberg, Germany. Elena.Tripel@med.uni-heidelberg.de.
Marcus SchiltenwolfUniversity Clinic of Heidelberg, Clinic for Orthopaedic and Trauma Surgery, Schlierbacher, Landstr, 200a 69118 Heidelberg, Germany. Marcus.Schiltenwolf@med.uni-heidelberg.de.
Johannes KirschUniversity Clinic of Heidelberg, Clinic for Orthopaedic and Trauma Surgery, Schlierbacher, Landstr, 200a 69118 Heidelberg, Germany. Johannes.Kirsch@med.uni-heidelberg.de.
Sébastien HagmannUniversity Clinic of Heidelberg, Clinic for Orthopaedic and Trauma Surgery, Schlierbacher, Landstr, 200a 69118 Heidelberg, Germany. Sebastien.Hagmann@med.uni-heidelberg.de.
Babak MoradiUniversity Clinic of Heidelberg, Clinic for Orthopaedic and Trauma Surgery, Schlierbacher, Landstr, 200a 69118 Heidelberg, Germany. babak.moradi@med.uni-heidelberg.de.
Heidelberg University · DEBrigham and Women's Hospital · US

Funding

Medizinischen Fakultät Heidelberg, Universität Heidelberg 0000
6 · The paper itself

Abstract

Osteoarthritis (OA) is a progressive joint disease driven by a blend of inflammatory and biomechanical processes. Studies using human samples to understand inflammatory mechanisms in OA frequently recruit OA patients with different affected joints, even though recent evidence indicates that OA is a heterogeneous disease which only culminates in a common end point. Differences in age of onset and the dynamics of disease progression suggest that different joints may represent different disease entities, thereby diluting the discovery potential in a combined analysis. We hypothesized that different OA joints may also differ in immunopathology within the synovium. To investigate this hypothesis, we profiled the immune cell contribution (flow cytometry) and cytokine release profiles (ELISA) in purified synovial membrane mononuclear cells from 50 patients undergoing either hip (

Indexed as

cytokinehipinflammationkneeosteoarthritissynovial membrane

Identifiers

PMID31590365
PMCPMC6832735
OpenAlexW2978629364

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.