Evidence map›Paper›PMID 39689029›Full record

ArticleRheumatology (Oxford, England)2025

Comorbidity in incident rheumatoid arthritis: a nationwide case-control study with bidirectional follow-up.

Bogdan Batko, Mateusz Szeląg, Magdalena Krajewska-Włodarczyk, Zbigniew Żuber, Michał Orleański, Krzysztof Podwójcic, Jakub Sowiński, Maria Świderek, Michał Maluchnik, Krzysztof Batko and 4 more

Abstract read
In one paragraph

Article in Rheumatology (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

14 authors.

Bogdan BatkoDepartment of Rheumatology and Immunology, Faculty of Medicine and Health Sciences, Andrzej Frycz Modrzewski University, Krakow, Poland.ORCID 0000-0003-3999-8093
Mateusz SzelągDepartment of Analysis and Strategy, Ministry of Health, Warsaw, Poland.
Magdalena Krajewska-WłodarczykClinic of Rheumatology, School of Medicine, Collegium Medicum, University of Warmia and Mazury, Olsztyn, Poland.
Zbigniew ŻuberDepartment of Pediatrics, Faculty of Medicine and Health Sciences, Andrzej Frycz Modrzewski University, Krakow, Poland.
Michał OrleańskiDepartment of Analysis and Strategy, Ministry of Health, Warsaw, Poland.
Krzysztof PodwójcicDepartment of Analysis and Strategy, Ministry of Health, Warsaw, Poland.
Jakub SowińskiDepartment of Analysis and Strategy, Ministry of Health, Warsaw, Poland.
Maria ŚwiderekDepartment of Analysis and Strategy, Ministry of Health, Warsaw, Poland.
Michał MaluchnikDepartment of Adult Neurology, Medical University of Gdansk, Gdansk, Poland.
Krzysztof BatkoDepartment of Dermatology, University Hospital, Krakow, Poland.
Agata ŚmiglewskaDepartment of Analysis and Strategy, Ministry of Health, Warsaw, Poland.
Marek BrzoskoDepartment of Rheumatology, Internal Diseases, Geriatrics and Clinical Immunology, Faculty of Medicine and Dentistry, Pomeranian Medical University, Szczecin, Poland.
Marcin StajszczykDepartment of Rheumatology and Autoimmune Diseases, Silesian Center for Rheumatology, Ustroń, Poland.
Brygida KwiatkowskaClinic of Early Arthritis, National Institute of Geriatrics, Rheumatology and Rehabilitation, Warsaw, Poland.

Funding

European Regional Development FundEuropean Social FundEuropean UnionIntegrated Analytical Platform POPC.02.02.00-00-0015/18-00Maps of Health Needs-Database of Systematic and Implementation Analysis POWR.05.02.00-00-0149/15
6 · The paper itself

Abstract

objectivesTo investigate the association between risk of different concurrent disorders and diagnosis of rheumatoid arthritis (RA) using a temporal approach.

methodsRetrospective, case-control study. Data were extracted from all available healthcare claims for Poland between 2011-2021. Prevalent RA (n = 262 265) patients were examined to evaluate morbidity patterns. Incident RA (n = 15 879) and age-, sex- and region-matched controls were sampled 1:10 from the general population (GP). Exposure was new-onset RA identified by interspaced, repeat claims and prescription. Follow-up was performed in a bidirectional, five-year timeframe from RA diagnosis (Dx).

resultsRA is associated with enhanced risk of multiple concomitant disorders both pre- and post-Dx, especially hematologic (incidence rate ratio (IRR) 1.80, 95% CI 1.58, 2.05), pulmonary (IRR 1.57, 95% CI 1.53, 1.62), gastrointestinal (IRR 1.53, 95% CI 1.46, 1.60) and cardiovascular (IRR 1.25, 95% CI 1.22, 1.27) conditions. RA appears strongly associated with interstitial lung disease (pre-Dx IRR 2.97, 95% CI 2.20, 4.02; post-Dx IRR 4.66, 95% CI 3.91, 5.56) and inflammatory bowel disease (pre-Dx IRR 1.61, 95% CI 1.25, 2.07; post-Dx IRR 2.12, 95% CI 1.70, 2.63). Enhanced post-Dx risk of thyroid cancer (IRR 1.29, 95% CI 1.00, 1.66) and lymphoma (IRR 1.50, 95% CI 1.20, 1.88) was observed, in contrast to reduced risk of colon cancer (IRR 0.77, 95% CI 0.62, 0.94).

conclusionEnhanced risk of multiple concurrent disorders was observed both pre- and post-RA Dx, with varying patterns across different disease groups. These data highlight the multisystemic nature of RA and warrant further research into causal, bidirectional relationships.

Indexed as

Arthritis, RheumatoidAdultAgedCardiovascular DiseasesCase-Control StudiesComorbidityFemaleFollow-Up StudiesGastrointestinal DiseasesHumansIncidenceLung Diseases, InterstitialMaleMiddle AgedPolandRetrospective Studiescardiovascularcomorbidityepidemiologicmorbidityneoplasmrheumatoid arthritisrisk factor

Identifiers

PMID39689029
PMCPMC12107052

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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.