Evidence mapPaperPMID 40580298Full record

ReviewInflammopharmacology2025

Protease activated receptor inhibitors in rheumatoid arthritis: a new frontier in treatment.

Tayyaba Rana, Huma Hameed, Ana Cláudia Paiva-Santos, Muhammad Jamshaid, Muneeba Anwar

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In one paragraph

Review in Inflammopharmacology, 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

5 authors.

Tayyaba RanaFaculty of Pharmaceutical Sciences, University of Central Punjab (UCP), Lahore, 54000, Pakistan.
Huma HameedFaculty of Pharmaceutical Sciences, University of Central Punjab (UCP), Lahore, 54000, Pakistan. huma.hameed@ucp.edu.pk.ORCID http://orcid.org/0000-0002-8636-8644
Ana Cláudia Paiva-SantosDepartment of Pharmaceutical Technology, Faculty of Pharmacy of the University of Coimbra, University of Coimbra, 3000-548, Coimbra, Portugal.ORCID http://orcid.org/0000-0003-2710-6000
Muhammad JamshaidFaculty of Pharmaceutical Sciences, University of Central Punjab (UCP), Lahore, 54000, Pakistan.
Muneeba AnwarFaculty of Pharmaceutical Sciences, University of Central Punjab (UCP), Lahore, 54000, Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rheumatoid arthritis (RA) is an autoimmune condition that involves inflammation of the joints, cartilage destruction, and progressive bone loss. RA is a disabling disease that may result in poor quality of life and permanent physical disability. Current interventions like NSAIDs, DMARDs, and biologics are more symptom-relieving and disease-preventing. But the increased risk of side effects, impaired immune system, and variability in efficacy restrict the efficacy and safety of such agents. The literature has brought to the forefront the pivotal role of Protease-activated receptors (PARs) in initiating inflammatory cascade, immune reactions, and progressive joint destruction. The main purpose of this review is to determine the potential of PAR inhibitors as an alternate treatment strategy for RA patients. In-vitro and in-vivo experiments have brought to the forefront the role of PAR inhibitors, like PAR-1 and PAR-2, in the modulation of bone cell activity, inhibition of cartilage destruction, and prevention of joint inflammation, and joint pain. Even though these observations are encouraging, we have yet to confirm the efficacy, safety, and specificity of PAR inhibitors. This review brings to the forefront the necessity to perform well-designed clinical trials with large sample sizes, to design specific and selective PAR inhibitors, and to explore the benefit of combination therapies in the treatment of RA.

Indexed as

Antirheumatic AgentsArthritis, RheumatoidReceptors, Proteinase-ActivatedAnimalsHumansInflammationAntirheumatic AgentsReceptors, Proteinase-ActivatedDrug deliveryInflammatory cytokinesProtease-activated receptorsRheumatoid arthritisTargeted therapies

Identifiers

What Socratic holds

Textmetadata
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 Socratic graph.