Evidence map›Paper›PMID 31557169›Full record

ArticlePloS one2019

Human osteocyte expression of Nerve Growth Factor: The effect of Pentosan Polysulphate Sodium (PPS) and implications for pain associated with knee osteoarthritis.

Catherine J M Stapledon, Helen Tsangari, Lucian B Solomon, David G Campbell, Plinio Hurtado, Ravi Krishnan, Gerald J Atkins

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 10% 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, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

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  8. Inhibition of CGRP signaling impairs fracture healing in mice.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 1 country.

Catherine J M StapledonCentre for Orthopaedic & Trauma Research, The University of Adelaide, Adelaide, South Australia, Australia.
Helen TsangariCentre for Orthopaedic & Trauma Research, The University of Adelaide, Adelaide, South Australia, Australia.
Lucian B SolomonCentre for Orthopaedic & Trauma Research, The University of Adelaide, Adelaide, South Australia, Australia.
David G CampbellCentre for Orthopaedic & Trauma Research, The University of Adelaide, Adelaide, South Australia, Australia.
Plinio HurtadoRenal Unit, Royal Adelaide Hospital, Adelaide, South Australia, Australia.
Ravi KrishnanParadigm Biopharmaceuticals Ltd., Melbourne, Victoria, Australia.
Gerald J AtkinsCentre for Orthopaedic & Trauma Research, The University of Adelaide, Adelaide, South Australia, Australia.ORCID 0000-0002-3123-9861
The University of Adelaide · AURoyal Adelaide Hospital · AUCalvary Wakefield Hospital · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pentosan polysulphate sodium (PPS) is a promising therapeutic agent for blocking knee pain in individuals with knee osteoarthritis (KOA). The mode of action of PPS in this context is unknown. We hypothesised that the osteocyte, being the principal cell type in the sub-chondral bone, was capable of expressing the pain mediator Nerve Growth Factor (NGF), and that this may be altered in the presence of PPS. We tested the expression of NGF and the response to PPS in the presence or absence of the proinflammatory cytokine tumour necrosis factor-alpha (TNFα), in human osteocytes. For this we differentiated human primary osteoblasts grown from subchondral bone obtained at primary knee arthroplasty for KOA to an osteocyte-like stage over 28d. We also tested NGF expression in fresh osteocytes obtained by sequential digestion from KOA bone and by immunofluorescence in KOA bone sections. We demonstrate for the first time the production and secretion of NGF/proNGF by this cell type derived from patients with KOA, implicating osteocytes in the pain response in this pathological condition and possibly others. PPS inhibited TNFα-induced levels of proNGF secretion and TNFα induced NGF mRNA expression. Together, this provides evidence that PPS may act to suppress the release of NGF in the subchondral bone to ameliorate pain associated with knee osteoarthritis.

Indexed as

AgedArthralgiaFemaleHumansNerve Growth FactorOsteoarthritis, KneeOsteocytesPentosan Sulfuric PolyesterTranscriptomeTumor Necrosis Factor-alphaNerve Growth FactorPentosan Sulfuric PolyesterTumor Necrosis Factor-alpha

Identifiers

PMID31557169
PMCPMC6762051
OpenAlexW2975015014

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.