Evidence map›Paper›PMID 42684644›Full record

ArticleInternal and emergency medicine2026

Unsupervised machine learning with Cluster Analysis in patients with rheumatoid arthritis: insights in CV risk phenotypes from a multicentre Italian cohort.

Vincenzo Venerito, Elena Bartoloni, Gian Luca Erre, Matteo Piga, Garifallia Sakellariou, Ombretta Viapiana, Andreina Manfredi, Elisa Gremese, Fabiola Atzeni, Francesca Romana Spinelli and 1 more

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Article in Internal and emergency medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Vincenzo VeneritoRheumatology Unit, Department of Precision and Regenerative Medicine and Ionian Area (DePReMeI), Università Degli Studi "Aldo Moro", Bari, Italy.
Elena BartoloniRheumatology Unit, Department of Medicine and Surgery, University of Perugia, Perugia, Italy.
Gian Luca ErreDipartimento Di Scienze Mediche, Chirurgiche E Sperimentali, Università Degli Studi di Sassari, Sassari, Italy.
Matteo PigaRheumatology Unit, AOU Cagliari, and Department of Medical Sciences and Public Health, University of Cagliari, Cagliari, Italy.
Garifallia SakellariouDepartment of Internal Medicine and Therapeutics, University of Pavia, Pavia, Italy.
Ombretta ViapianaRheumatology Unit, Department of Medicine, University and Azienda Ospedaliera Universitaria Integrata of Verona, Verona, Italy.
Andreina ManfrediRheumatology Unit, Azienda Ospedaliera Universitaria Policlinico of Modena, Modena, Italy.
Elisa GremeseRheumatology and Clinical Immunology, IRCCS Humanitas Research Hospital, Rozzano, Italy.
Fabiola AtzeniRheumatology Unit, Department of Experimental and Internal Medicine, University of Messina, Messina, Italy.
Francesca Romana SpinelliRheumatology Unit, Department of Medical and Cardiovascular Sciences, Sapienza University of Rome, Rome, Italy. francescaromana.spinelli@uniroma1.it.ORCID http://orcid.org/0000-0003-1969-2097
Fabio CacciapagliaRheumatology Unit, Department of Precision and Regenerative Medicine and Ionian Area (DePReMeI), Università Degli Studi "Aldo Moro", Bari, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rheumatoid arthritis (RA) patients face increased cardiovascular (CV) risk, yet existing 10-year estimation tools often underperform. This study evaluated whether unsupervised machine learning (uML) clustering can identify distinct RA patient phenotypes with varying major cardiovascular events (MACE) potentially improving risk stratification. A cross-sectional, multi-center cohort of RA patients meeting the 2010 ACR/EULAR classification criteria and without prior CV events was enrolled in January 2019 and followed-up for MACE incidence over 5 years. Clinical and demographic data, including traditional CV risk factors and SCORE2 estimates, were collected. Factor Analysis of Mixed Data (FAMD), a generalization of principal component analysis for mixed data types, was applied in Python (ver.3.9) using Prince (ver.0.7.1). Missing data observations were excluded. Bootstrapped eigenvalue distribution determined the number of FAMD components for clustering, followed by Hierarchical Clustering on Principal Components using Ward's criterion and Euclidean distance. An XGBoost model assessed feature importance, while ANOVA and Chi-square tests evaluated cluster differences. Among 951 RA patients (mean age 61.8 ± 10.5 years; 81.1% female; median disease duration 120 months), 9 MACE occurred (incidence: 1.89/1000 patient-years). Four clusters emerged: Cluster 1 (high HAQ, steroid use, high cholesterol), Cluster 2 (low disease activity, BMI, diabetes, hypertension, SCORE2), Cluster 3 (predominantly male, < 10-year disease duration, csDMARDs; no MACE cases), and Cluster 4 (longer disease duration, hypertension, high triglycerides, lipid-lowering agents, TNFi; highest MACE incidence).uML clustering identified distinct RA phenotypes, complementing SCORE2 for improved CV risk stratification and aiding in recognizing patients at elevated MACE risk.

Indexed as

Cardiovascular riskMachine learningMajor cardiovascular eventsRheumatoid arthritisRisk stratificationSCORE2Unsupervised clustering

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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.