Evidence map›Paper›PMID 23830938›Full record

ReviewGene2013

A current review of molecular mechanisms regarding osteoarthritis and pain.

Andrew S Lee, Michael B Ellman, Dongyao Yan, Jeffrey S Kroin, Brian J Cole, Andre J van Wijnen, Hee-Jeong Im

Open access · greenAbstract readReview
In one paragraph

Review in Gene, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 180 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
180citing papers in PubMed, 3 pooled it
27.7field-weighted citation impact, top 1% 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

180 citing papers in PubMed, 3 syntheses or guidelines pooled it, 411 citations in OpenAlex.

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  16. Regenerative Medicine: The Next Generation of Autologous Blood Formulations.HSS journal : the musculoskeletal journal of Hospital for Special Surgery · 2025
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120 more citing papers are in PubMed but not listed here.

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 4 institutions in 1 country.

Andrew S LeeDepartment of Biochemistry, Rush University Medical Center, University of Illinois, Chicago, IL 60612, USA.
Michael B Ellman
Dongyao Yan
Jeffrey S Kroin
Brian J Cole
Andre J van Wijnen
Hee-Jeong Im
University of Illinois Chicago · USMayo Clinic in Arizona · USRush University Medical Center · USUniversity of Illinois Urbana-Champaign · US

Funding

Molecular Control of Bone FormationR01AR049069 · NIAMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI WESTENDORF, JENNIFER J · 2003 to 2021
$5.8M
Pain Mechanisms of Knee Joint OsteoarthritisR01AR062136 · NIAMS · RUSH UNIVERSITY MEDICAL CENTER · PI CHEN, DI · 2012 to 2016
$1.7M
Pathological Role of bFGF in Human Adult Articular CartilageR01AR053220 · NIAMS · RUSH UNIVERSITY MEDICAL CENTER · PI SAMPEN, HEE-JEONG IM · 2006 to 2010
$1.6M
OSTEOARTHRITIS AND KNEE JOINT PAINI01BX002647 · VA · JESSE BROWN VA MEDICAL CENTER · PI SAMPEN, HEE-JEONG IM · 2015 to 2023
–
BLRD VA I01 BX002647NIAMS NIH HHS AR053220NIAMS NIH HHS AR062136NIAMS NIH HHS R01 AR049069NIAMS NIH HHS R01AR049069NIAMS NIH HHS R01 AR053220NIAMS NIH HHS R01 AR062136
6 · The paper itself

Abstract

Osteoarthritis afflicts millions of individuals across the world resulting in impaired quality of life and increased health costs. To understand this disease, physicians have been studying risk factors, such as genetic predisposition, aging, obesity, and joint malalignment; however have been unable to conclusively determine the direct etiology. Current treatment options are short-term or ineffective and fail to address pathophysiological and biochemical mechanisms involved with cartilage degeneration and the induction of pain in arthritic joints. OA pain involves a complex integration of sensory, affective, and cognitive processes that integrate a variety of abnormal cellular mechanisms at both peripheral and central (spinal and supraspinal) levels of the nervous system Through studies examined by investigators, the role of growth factors and cytokines has increasingly become more relevant in examining their effects on articular cartilage homeostasis and the development of osteoarthritis and osteoarthritis-associated pain. Catabolic factors involved in both cartilage degradation in vitro and nociceptive stimulation include IL-1, IL-6, TNF-α, PGE2, FGF-2 and PKCδ, and pharmacologic inhibitors to these mediators, as well as compounds such as RSV and LfcinB, may potentially be used as biological treatments in the future. This review explores several biochemical mediators involved in OA and pain, and provides a framework for the understanding of potential biologic therapies in the treatment of degenerative joint disease in the future.

Indexed as

HumansOsteoarthritisPainADAMTS-4a disintergrin and metalloproteinase with thrombospondin motifsAnti-IL-1anti-interleukin 1Biochemical mediatorsBMP-7bone morphogenetic protein 7bovine lactoferrincAMPCartilagec-Jun N-terminal kinaseCOXcyclic adenosine monophosphatecyclooxygenasedorsal root ganglionDRGECMEPE prostanoid receptorERKextracellular matrixextracellular signal-regulated kinaseFGF-2FGFR1-Rasfibroblast growth factor 2fibroblast growth factor receptor 1-Rasfibronectin fragmentFn-fIGF-1ILIL-1raIL-1βinducible nitric oxide synthaseiNOSinsulin-like growth factor 1interleukininterleukin-1 betainterleukin-1 receptor antagonistintervertebral diskIVDJNKlactoferrinleukemia inducing factorLfLfcinBLIFMAPKsmatrix metalloproteinasemessenger ribonucleic acidmicrosomal prostaglandin E synthase-1mitogen-activated protein kinaseMMPmPGES-1mRNANFκBnonsteroidal anti-inflammatory drugsNSAIDSnuclear factor kappa-light-chain-enhancer of activated B cellsOAOsteoarthritic painosteoarthritisOsteoarthritisPGPGD2PGE2PGESPGE synthasePGF2FaPGI2PKCδprostaglandin D2prostaglandin E2prostaglandin fibroblast growth factor alphaprostaglandin I2protein kinase C alphaproteoglycanRAreactive oxygen speciesresveratrolrheumatoid arthritisribonucleic acidRNAROSRSVSPsubstance PTNFRTNF-αtumor necrosis factor alphatumor necrosis factor receptor

Identifiers

PMID23830938
PMCPMC3745800
OpenAlexW2164531777

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.