Evidence map›Paper›PMID 42402554›Full record

ReviewClinical proteomics2026

Proteomic and glycosylation biomarkers in rheumatoid arthritis: advancing early diagnosis and precision therapy.

Preeti Sharma, Shahbaz Aman, Priya Koundal, Shakeel Ahmed Mohammed, Hardeep Kaur, Faraz Ahmad, Sabiha Khatoon, Shafiul Haque, Arif Hussain

Abstract readReview
In one paragraph

Review in Clinical proteomics, 2026. 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

9 authors.

Preeti SharmaDepartment of Biochemistry, MM Institute of Medical Sciences and Research, Maharishi Markandeshwar (Deemed to be University), Mullana-Ambala, Haryana, 133207, India.
Shahbaz AmanDepartment of Microbiology, MM Institute of Medical Sciences and Research, Maharishi Markandeshwar (Deemed to be University), Mullana-Ambala, Haryana, 133207, India. shahbazaman095@gmail.com.
Priya KoundalDepartment of Biochemistry, MM Institute of Medical Sciences and Research, Maharishi Markandeshwar (Deemed to be University), Mullana-Ambala, Haryana, 133207, India.
Shakeel Ahmed MohammedDepartment of Biosciences & Technology and Central Research Cell, MM Engineering College, Maharishi Markandeshwar (Deemed to be University), Mullana-Ambala, Haryana, 133207, India.
Hardeep KaurDepartment of Zoology, Ramjas College, University of Delhi, Delhi, 110007, India.ORCID http://orcid.org/0000-0002-7136-7972
Faraz AhmadDepartment of Integrative Biology, School of Bio Sciences and Technology (SBST), Vellore Institute of Technology (VIT), Vellore, India.ORCID http://orcid.org/0000-0003-4284-8045
Sabiha KhatoonDepartment of Biochemistry and Physiology, Oklahoma University health Sciences Center, Oklahoma City, OK, 73104, USA.
Shafiul HaqueDepartment of Nursing, College of Nursing and Health Sciences, Jazan University, Jazan, Saudi Arabia.
Arif HussainManipal Institute of Health & Life Sciences (MIHLS), Manipal Academy of Higher Education, Dubai Campus, G04, Dubai International Academic City (DIAC), 345050, Dubai, United Arab Emirates. arifhussain@manipaldubai.com.ORCID http://orcid.org/0000-0002-0851-4845

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRheumatoid arthritis (RA) is a chronic autoimmune disease characterized by progressive joint inflammation and damage. Early clinical diagnosis is crucial for effective intervention but presents significant challenges due to an initial asymptomatic inflammatory phase. MAIN BODY: Anti-citrullinated-protein antibodies (ACPA) and rheumatoid factor (RF) detection have been useful in early RA diagnosis, but their reliability is debatable as they are often non-specific. This has prompted a quest for alternative, more robust biomarkers. Researchers have turned to advanced proteomic and glycosylation analyses of biological fluids (e.g., synovial fluid, plasma and serum) and tissues using techniques such as MALDI-MS, Q-TOF, and SELDI-TOF. These approaches may offer a comprehensive approach to scrutinize a range of biomolecules as potential RA biomarkers, from citrullinated-proteins and peptides to novel potential protein biomarkers such as thymosin, macrophage-capping protein, calgranulins, and serum amyloid-A. Further, proteomics-based approaches have the ability to specifically monitor changes in the RA proteome (e.g., glycosylated VCAM1/SEMA4D proteins and GFAP/A1BG auto-antibodies) to unearth potential diagnostic and prognostic candidates. Disease monitoring in response to anti-rheumatic drugs using treatment-responsive markers, such as S100A8/A9 heterocomplex and leucine-rich alpha-2 glycoprotein, is another application of proteomics-based technologies.

conclusionIn view of the significance of prediction, early diagnosis and monitoring of RA symptomatology, this review discusses the potential utilities of proteinaceous species as proteomics-based biomarkers that may provide insights into disease mechanisms and offer potential avenues for personalized therapeutic interventions to revolutionize RA management.

Indexed as

BiomarkersDiagnosticsDisease monitoringProteomicsRheumatoid arthritisTherapeutics

Identifiers

PMID42402554
PMCPMC13629044

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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.