Evidence map›Paper›PMID 41695577›Full record

ArticleRheumatology advances in practice2026

Patterns and risk of cardiovascular disease in rheumatoid arthritis and psoriatic arthritis: a nationwide cohort study in the UK.

Zijing Yang, Fabiola Atzeni, Mark Russell, Kaiyang Song, Callum Coalwood, Elizabeth Price, Maya Buch, Sam Norton, James Galloway

Abstract read
In one paragraph

Article in Rheumatology advances in practice, 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

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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
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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.

Zijing YangDepartment of Inflammation Biology, Centre for Rheumatic Diseases, King's College London, London, UK.
Fabiola AtzeniDepartment of Experimental and Internal Medicine, University of Messina, Messina, Italy.
Mark RussellDepartment of Inflammation Biology, Centre for Rheumatic Diseases, King's College London, London, UK.ORCID https://orcid.org/0000-0001-8171-7772
Kaiyang SongDepartment of Inflammation Biology, Centre for Rheumatic Diseases, King's College London, London, UK.
Callum CoalwoodNational Early Inflammatory Autoimmune Diseases Audit, British Society for Rheumatology, London, UK.
Elizabeth PriceDepartment of Rheumatology, Great Western Hospital NHS Foundation Trust, Swindon, UK.ORCID https://orcid.org/0000-0003-3042-0201
Maya BuchCentre for Musculoskeletal Research, University of Manchester, Manchester, UK.ORCID https://orcid.org/0000-0002-8962-5642
Sam NortonDepartment of Inflammation Biology, Centre for Rheumatic Diseases, King's College London, London, UK.ORCID https://orcid.org/0000-0003-1714-9963
James GallowayDepartment of Inflammation Biology, Centre for Rheumatic Diseases, King's College London, London, UK.ORCID https://orcid.org/0000-0002-1230-2781

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Patients with inflammatory arthritis (IA), including RA and PsA, have an elevated cardiovascular disease (CVD) risk. It is unclear whether this persists in the modern treat-to-target era, particularly in early disease. This study evaluates CVD risk and mortality in a contemporary early RA and PsA cohort. Methods: Adults (≥18 years) with newly diagnosed RA or PsA registered in the National Early Inflammatory Arthritis Audit (NEIAA) from 2018 to 2023 were included. Incidence rates of CVD events, major adverse cardiovascular events (MACE) and all-cause and CVD mortality were calculated. Standardized incidence and mortality ratios compared outcomes with the general population. Competing risk regression assessed factors associated with CVD outcomes. Results: A total of 1012/17 669 RA and 104/3271 PsA participants had CVD hospitalizations. The incidence of MACE hospitalizations was 2.4/100 person-years (95% CI 2.2, 2.7) in RA and 0.6/100 person-years (95% CI 0.4, 1.0) in PsA. The risk of CVD hospitalizations was ≈25% higher in IA participants. Compared with the general population, all-cause mortality was 1.1 times higher in RA. CVD incidence and mortality were consistently higher in males. Hypertension, diabetes and smoking were associated with an increased CVD risk. Early corticosteroid use did not predict CVD, while better early RA treatment response was linked to lower CVD risk. Conclusion: A greater incidence of CVD and MACE exists in early IA, although less than previously reported. Traditional CVD risk factors are the dominant explanation for the risk increase, with disease control being a smaller but significant contributor to risk. Routine cardiovascular risk assessment in early IA remains justified.

Indexed as

cardiovascular riskpsoriatic arthritisrheumatoid arthritis

Identifiers

PMID41695577
PMCPMC12900542

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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.