Evidence map›Paper›PMID 41409165›Full record

ReviewACS pharmacology & translational science2025

Impact of Symptomatic Slow-Acting Drugs on Inflammatory Pathways in Osteoarthritis: Therapeutic Advances and Future Challenges.

Vitor Alfredo de Santana Silva, Katarine Gabriely Aurista do Nascimento, Priscila Gubert, Maria G Carneiro-da-Cunha, Kátia Alves Ribeiro, Paulo Antônio Galindo Soares

Abstract readReview
In one paragraph

Review in ACS pharmacology & translational science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Vitor Alfredo de Santana SilvaDepartment of Biochemistry/Keizo Asami Institute-iLIKA, Federal University of Pernambuco (UFPE), Av. Prof. Moraes Rego, s/n, Cidade Universitária, CEP: 50670-420 Recife, Pernambuco, Brazil.
Katarine Gabriely Aurista do NascimentoDepartment of Biochemistry/Keizo Asami Institute-iLIKA, Federal University of Pernambuco (UFPE), Av. Prof. Moraes Rego, s/n, Cidade Universitária, CEP: 50670-420 Recife, Pernambuco, Brazil.
Priscila GubertDepartment of Biochemistry/Keizo Asami Institute-iLIKA, Federal University of Pernambuco (UFPE), Av. Prof. Moraes Rego, s/n, Cidade Universitária, CEP: 50670-420 Recife, Pernambuco, Brazil.
Maria G Carneiro-da-CunhaDepartment of Biochemistry/Keizo Asami Institute-iLIKA, Federal University of Pernambuco (UFPE), Av. Prof. Moraes Rego, s/n, Cidade Universitária, CEP: 50670-420 Recife, Pernambuco, Brazil.
Kátia Alves RibeiroDepartment of Biochemistry/Keizo Asami Institute-iLIKA, Federal University of Pernambuco (UFPE), Av. Prof. Moraes Rego, s/n, Cidade Universitária, CEP: 50670-420 Recife, Pernambuco, Brazil.
Paulo Antônio Galindo SoaresDepartment of Biochemistry/Keizo Asami Institute-iLIKA, Federal University of Pernambuco (UFPE), Av. Prof. Moraes Rego, s/n, Cidade Universitária, CEP: 50670-420 Recife, Pernambuco, Brazil.ORCID https://orcid.org/0000-0002-3005-4099

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteoarthritis (OA) is a leading cause of physical disability, psychological distress, and a significant economic burden worldwide. Current treatments alleviate symptoms; however, disease progression remains largely uncontrolled, highlighting the urgent need for investigation of disease-modifying therapies. Symptomatic slow-acting drugs for osteoarthritis (SYSADOAs), such as glucosamine (GlcN), chondroitin sulfate (CS), and hyaluronic acid (HA), have gained increasing attention for their potential benefits in alleviating pain and mitigating the inflammatory and degenerative processes that characterize OA. These compounds modulate several homeostatic mechanisms, promoting anti-inflammatory, antioxidant, antiapoptotic, and anabolic countermensuring effects. Nevertheless, debates regarding their long-term efficacy and safety remain controversial, which explains why major osteoarthritis societies do not provide the same recommendations for the pharmacological treatment of OA. In this context, this review critically evaluates the current evidence surrounding HA, GlcN, and CS, highlighting their safety, mechanisms of action, and promising therapeutic perspectives for modifying the natural course of knee, hand, and hip OA.

Indexed as

chondroitin sulfateglucosaminehyaluronic acidinflammation

Identifiers

PMID41409165
PMCPMC12707266

What OpenQuestion holds

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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.