Evidence map›Paper›PMID 42088513›Full record

ReviewFrontiers in immunology2026

Transcriptomics and AI-driven approaches to the diagnosis and treatment of rheumatoid arthritis.

Marzena Ciechomska, Maciej Oldak, Magdalena Massalska

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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

3 authors.

Marzena CiechomskaDepartment of Pathophysiology and Immunology, National Institute of Geriatrics, Rheumatology, and Rehabilitation (NIGRiR), Warsaw, Poland.
Maciej OldakDepartment of Pathophysiology and Immunology, National Institute of Geriatrics, Rheumatology, and Rehabilitation (NIGRiR), Warsaw, Poland.
Magdalena MassalskaDepartment of Pathophysiology and Immunology, National Institute of Geriatrics, Rheumatology, and Rehabilitation (NIGRiR), Warsaw, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rheumatoid arthritis (RA) is a chronic autoimmune inflammatory disorder marked by joint swelling, pain, and progressive tissue destruction. Increasing evidence suggests that dysregulated RNA expression critically drives RA progression by perturbing immune, inflammatory, and stromal cell programs. These aberrant transcriptional signatures offer valuable biomarkers for diagnosis, prognosis, and therapeutic stratification. Recent advances in transcriptomic technologies have transformed our understanding of RA biology. Bulk RNA profiling has highlighted key dysregulated pathways and disease-associated molecular signatures. Single-cell transcriptomics has expanded this insight by defining extensive cellular heterogeneity and uncovering rare immune and stromal populations implicated in disease initiation, progression, and treatment response. The emergence of spatial transcriptomics provides an additional dimension by preserving tissue architecture, enabling precise localisation of pathogenic cell states and mapping cell-cell interactions within inflamed joints and other affected tissues. Integration of transcriptomic datasets with advanced computational and machine learning (ML) methods has accelerated biomarker discovery. Techniques such as Random Forest, XGBoost, support vector machines (SVM), artificial neural networks (ANNs), and Least Absolute Shrinkage and Selection Operator (LASSO) regression facilitate feature selection and prediction from high-dimensional data. Complementary network- and pathway-based tools, including Weighted Gene Co-expression Network Analysis (WGCNA) and Gene Set Variation Analysis (GSVA), uncover co-regulated modules and refine clinically relevant signatures. Collectively, this review aims to provide an update on how the integration of transcriptomics, spatial technologies, and advanced algorithms offers powerful opportunities to identify novel biomarkers and pathogenic cell populations, thereby advancing precision medicine in RA.

Indexed as

Arthritis, RheumatoidArtificial IntelligenceTranscriptomeBiomarkersGene Expression ProfilingHumansMachine LearningBiomarkersalgorithmsartificial intelligencebiomarkersmachine learningprecision medicinerheumatoid arthritistranscriptomics

Identifiers

PMID42088513
PMCPMC13136271

What OpenQuestion holds

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LicenceCC BY
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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.