Evidence map›Paper›PMID 34209473›Full record

ArticleGenes2021

Synovium-Synovial Fluid Axis in Osteoarthritis Pathology: A Key Regulator of the Cartilage Degradation Process.

Dhanashri Ingale, Priya Kulkarni, Ali Electricwala, Alpana Moghe, Sara Kamyab, Suresh Jagtap, Aare Martson, Sulev Koks, Abhay Harsulkar

Open access · goldAbstract read
In one paragraph

Article in Genes, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
7.1field-weighted citation impact, top 2% 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

28 citing papers in PubMed, 43 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

9 authors at 4 institutions in 3 countries.

Dhanashri IngaleDepartment of Cell and Molecular Biology, Interactive Research School for Health Affairs (IRSHA), Bharati Vidyapeeth University, Pune 411043, India.
Priya KulkarniDepartment of Pathophysiology, Biomedicine and Translational Medicine, University of Tartu, Ravila 19, 50411 Tartu, Estonia.
Ali ElectricwalaElectricwala Hospital, A 4/1, Pleasant Park, Fatima Nagar, Wanowrie, Pune 411013, India.ORCID 0000-0002-7834-6277
Alpana MogheDepartment of Cell and Molecular Biology, Rajiv Gandhi Institute of IT and Biotechnology, Bharati Vidyapeeth University, Pune 411043, India.
Sara KamyabDepartment of Cell and Molecular Biology, Rajiv Gandhi Institute of IT and Biotechnology, Bharati Vidyapeeth University, Pune 411043, India.
Suresh JagtapHerbal Medicine, Interactive Research School for Health Affairs (IRSHA), Bharati Vidyapeeth University, Pune 411043, India.ORCID 0000-0002-6091-9583
Aare MartsonDepartment of Traumatology and Orthopedics, Tartu University Hospital, University of Tartu, L Puusepa 8, 51014 Tartu, Estonia.ORCID 0000-0003-4857-484X
Sulev KoksCentre for Molecular Medicine and Innovative Therapeutics, Murdoch University, Murdoch, WA 6150, Australia.ORCID 0000-0001-6087-6643
Abhay HarsulkarDepartment of Pathophysiology, Biomedicine and Translational Medicine, University of Tartu, Ravila 19, 50411 Tartu, Estonia.
Bharati Vidyapeeth Deemed University · INTartu University Hospital · EEMurdoch University · AUUniversity of Tartu · EE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Failure of conventional anti-inflammatory therapies in osteoarthritis (OA) underlines the insufficient knowledge about inflammatory mechanisms, patterns and their relationship with cartilage degradation. Considering non-linear nature of cartilage loss in OA, a better understanding of inflammatory milieu and MMP status at different stages of OA is required to design early-stage therapies or personalized disease management. For this, an investigation based on a synovium-synovial fluid (SF) axis was planned to study OA associated changes in synovium and SF along the progressive grades of OA. Gene expressions in synovial-biopsies from different grades OA patients (N = 26) revealed a peak of IL-1β, IL-15, PGE2 and NGF in early OA (Kellgren-Lawrence (KL) grade-I and II); the highest MMP levels were found in advanced stages (KL grade-III and IV). MMPs (MMP-1, 13, 2 and 9) abundance and FALGPA activity estimated in forty SFs of progressive grades showed the maximum protein levels and activity in KL grade-II and III. In an SF challenge test, SW982 and THP1 cells were treated with progressive grade SFs to study the dynamics of MMPs modulation in inflammatory microenvironment; the test yielded a result pattern, which matched with FALGPA and the protein-levels estimation. Inflammatory mediators in SFs served as steering factor for MMP up-regulation. A correlation-matrix of IL-1β and MMPs revealed expressional negative correlation.

Indexed as

CartilageDinoprostoneFemaleHumansInterleukin-15Interleukin-1betaMaleMatrix Metalloproteinase 1Nerve Growth FactorOligopeptidesOsteoarthritisOsteoarthritis, KneeSynovial FluidSynovial Membrane2-furanacryloyl-leucyl-glycyl-prolyl-alanineDinoprostoneIL1B protein, humanInterleukin-15Interleukin-1betaMatrix Metalloproteinase 1MMP1 protein, humanNerve Growth FactorOligopeptidesFALGPAinflammatory mediatorsKellgren–Lawrence radiographic gradesMMPsosteoarthritissynovial-fluidsynovitis

Identifiers

PMID34209473
PMCPMC8305855
OpenAlexW3175117783

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.