Evidence map›Paper›PMID 34848838›Full record

ReviewExperimental & molecular medicine2021

Disease-modifying therapeutic strategies in osteoarthritis: current status and future directions.

Yongsik Cho, Sumin Jeong, Hyeonkyeong Kim, Donghyun Kang, Jeeyeon Lee, Seung-Baik Kang, Jin-Hong Kim

Open access · goldAbstract readReview
In one paragraph

Review in Experimental & molecular medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 183 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
183citing papers in PubMed, 2 pooled it
28.9field-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

183 citing papers in PubMed, 2 syntheses or guidelines pooled it, 271 citations in OpenAlex.

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123 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 3 institutions in 2 countries.

Yongsik Cho *Department of Biological Sciences, College of Natural Sciences, Seoul National University, Seoul, 08826, South Korea.ORCID http://orcid.org/0000-0002-4788-3141
Sumin Jeong *Department of Biological Sciences, College of Natural Sciences, Seoul National University, Seoul, 08826, South Korea.
Hyeonkyeong KimDepartment of Biological Sciences, College of Natural Sciences, Seoul National University, Seoul, 08826, South Korea.
Donghyun KangDepartment of Biological Sciences, College of Natural Sciences, Seoul National University, Seoul, 08826, South Korea.ORCID http://orcid.org/0000-0003-1966-1397
Jeeyeon LeeDepartment of Biological Sciences, College of Natural Sciences, Seoul National University, Seoul, 08826, South Korea.ORCID http://orcid.org/0000-0001-6489-1832
Seung-Baik KangDepartment of Orthopaedic Surgery, Seoul National University College of Medicine, Boramae Hospital, Seoul, 07061, South Korea. ssbkang@snu.ac.kr.
Jin-Hong KimDepartment of Biological Sciences, College of Natural Sciences, Seoul National University, Seoul, 08826, South Korea. jinhkim@snu.ac.kr.ORCID http://orcid.org/0000-0002-6480-1929
Seoul National University · KRInstitute for Basic Science · KRSeoul National University of Science and Technology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteoarthritis (OA) is the most common form of arthritis. It is characterized by progressive destruction of articular cartilage and the development of chronic pain and constitutes a considerable socioeconomic burden. Currently, pharmacological treatments mostly aim to relieve the OA symptoms associated with inflammation and pain. However, with increasing understanding of OA pathology, several potential therapeutic targets have been identified, enabling the development of disease-modifying OA drugs (DMOADs). By targeting inflammatory cytokines, matrix-degrading enzymes, the Wnt pathway, and OA-associated pain, DMOADs successfully modulate the degenerative changes in osteoarthritic cartilage. Moreover, regenerative approaches aim to counterbalance the loss of cartilage matrix by stimulating chondrogenesis in endogenous stem cells and matrix anabolism in chondrocytes. Emerging strategies include the development of senolytic drugs or RNA therapeutics to eliminate the cellular or molecular sources of factors driving OA. This review describes the current developmental status of DMOADs and the corresponding results from preclinical and clinical trials and discusses the potential of emerging therapeutic approaches to treat OA.

Indexed as

AnimalsAnti-Inflammatory AgentsBiomarkersCartilage, ArticularCombined Modality TherapyCytokinesDisease ManagementDisease SusceptibilityDrug DevelopmentHumansMolecular Targeted TherapyOsteoarthritisSignal TransductionAnti-Inflammatory AgentsBiomarkersCytokines

Identifiers

PMID34848838
PMCPMC8640059
OpenAlexW3215837414

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.