Evidence map›Paper›PMID 27176565›Full record

ReviewJournal of orthopaedic research : official publication of the Orthopaedic Research Society2017

Intra-articular dexamethasone to inhibit the development of post-traumatic osteoarthritis.

Alan J Grodzinsky, Yang Wang, Sanjeev Kakar, Mark S Vrahas, Christopher H Evans

Open access · bronzeAbstract readReview
In one paragraph

Review in Journal of orthopaedic research : official publication of the Orthopaedic Research Society, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
7.2field-weighted citation impact, top 3% 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

49 citing papers in PubMed, 87 citations in OpenAlex.

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  14. Osteoarthritis and cartilage open · 2024
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  16. A review of advanced hydrogels for cartilage tissue engineering.Frontiers in bioengineering and biotechnology · 2024
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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

5 authors at 4 institutions in 1 country.

Alan J GrodzinskyDepartments of Biological, Electrical and Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts.
Yang WangDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts.
Sanjeev KakarDepartment of Orthopaedic Surgery, Mayo Clinic, Rochester, Minnesota.
Mark S VrahasDepartment of Orthopaedic Surgery, Harvard Medical School, Boston, Massachusetts.
Christopher H EvansRehabilitation Medicine Research Center, Mayo Clinic, Rochester, Minnesota.
Massachusetts Institute of Technology · USHarvard University · USMayo Clinic · USWinnMed · US

Funding

Cartilage Repair Using Self Assembling Peptide ScaffoldsR01AR060331 · NIAMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI GRODZINSKY, ALAN J. · 2012 to 2016
$1.7M
ELECTROMECHANICS OF CARTILAGE: SYNTHESIS &DEGRADATIIONR01AR033236 · NIAMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI GRODZINSKY, ALAN J. · 1986 to 2010
$1.5M
CARTILAGE METABOLIC RESPOSE TO LOADING: TARGET MOLECULESR37AR033236 · NIAMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI GRODZINSKY, ALAN J · 1995 to 2004
$1.2M
NIAMS NIH HHS R01 AR033236NIAMS NIH HHS R01 AR060331NIAMS NIH HHS R37 AR033236
6 · The paper itself

Abstract

Injury to the joint provokes a number of local pathophysiological changes, including synthesis of inflammatory cytokines, death of chondrocytes, breakdown of the extra-cellular matrix of cartilage, and reduced synthesis of matrix macromolecules. These processes combine to engender the subsequent development of post-traumatic osteoarthritis (PTOA). To prevent this from happening, it is necessary to inhibit these disparate responses to injury; given their heterogeneity, this is challenging. However, dexamethasone has the necessary pleiotropic properties required of a drug for this purpose. Using in vitro models, we have shown that low doses of dexamethasone sustain the synthesis of cartilage proteoglycans while inhibiting their breakdown after injurious compression in the presence or absence of inflammatory cytokines. Under these conditions, dexamethasone is non-toxic and maintains the viability of chondrocytes exposed chronically to such cytokines as interleukin (IL) -1, IL-6, and tumor necrosis factor-α. Moreover, the anti-inflammatory properties of dexamethasone have been appreciated for decades. In view of this information, we have initiated a pilot clinical study to determine whether a single, intra-articular injection of dexamethasone into the wrist shows promise in preventing PTOA after intra-articular fracture of the distal radius. CLINICAL SIGNIFICANCE: Suppressing the various etiopathophysiological responses to injury in the joint is an attractive strategy for lowering the clinical burden of PTOA. The intra-articular administration of dexamethasone soon after injury offers a simple and inexpensive means of accomplishing this. © 2017 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 35:406-411, 2017.

Indexed as

AnimalsCartilage, ArticularClinical Trials as TopicDexamethasoneGlucocorticoidsHumansInflammationJointsOsteoarthritisWounds and InjuriesDexamethasoneGlucocorticoidscartilagehand and wristpathophysiologysynovium and osteoarthritistrauma

Identifiers

PMID27176565
PMCPMC5604325
OpenAlexW2416986411

What OpenQuestion holds

Textmetadata
LicenceTDM
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.