Evidence map›Paper›PMID 42260503›Full record

ArticleRespiratory research2026

Genetic and epidemiological evidence linking respiratory and musculoskeletal diseases: shared risk factors and intervention windows.

Olivia Murrin, Bethany Voller, Ruby M Woodward, Lucía A Carrasco-Ribelles, Deniz Türkmen, Qingze Gu, Kate Boddy, Leon Farmer, Mary Mancini, Sara Khalid and 10 more

Abstract read
In one paragraph

Article in Respiratory research, 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

20 authors.

Olivia MurrinDepartment of Clinical and Biomedical Sciences, Faculty of Health and Life Sciences, University of Exeter, Exeter, UK. o.murrin@exeter.ac.uk.
Bethany VollerDepartment of Clinical and Biomedical Sciences, Faculty of Health and Life Sciences, University of Exeter, Exeter, UK.
Ruby M WoodwardDivision of Public Health & Epidemiology, School of Medical Sciences, University of Leicester, Leicester, UK.
Lucía A Carrasco-RibellesUnitat de Suport a La Recerca Metropolitana Nord, Fundacio Institut Universitari Per a La Recerca a L'Atencio Primaria de Salut Jordi Gol I Gurina (IDIAPJGol), Barcelona, 08007, Spain.
Deniz TürkmenDepartment of Clinical and Biomedical Sciences, Faculty of Health and Life Sciences, University of Exeter, Exeter, UK.
Qingze GuNuffield Department of Orthopaedics Rheumatology and Musculoskeletal Sciences, Centre for Statistics in Medicine, University of Oxford, Oxford, UK.
Kate BoddyDepartment of Health and Community Sciences, Faculty of Health and Life Sciences, University of Exeter, Exeter, UK.
Leon FarmerPublic and Patient Involvement Representative, Exeter, UK.
Mary ManciniPublic and Patient Involvement Representative, Exeter, UK.
Sara KhalidNuffield Department of Orthopaedics Rheumatology and Musculoskeletal Sciences, Centre for Statistics in Medicine, University of Oxford, Oxford, UK.
Nicholas AveyardDepartment of Clinical and Biomedical Sciences, Faculty of Health and Life Sciences, University of Exeter, Exeter, UK.
Chris FoxDepartment of Health and Community Sciences, Faculty of Health and Life Sciences, University of Exeter, Exeter, UK.
Jack BowdenDepartment of Clinical and Biomedical Sciences, Faculty of Health and Life Sciences, University of Exeter, Exeter, UK.
Frank DudbridgeDivision of Public Health & Epidemiology, School of Medical Sciences, University of Leicester, Leicester, UK.
Sarah E LambDepartment of Public Health and Sports Sciences, Faculty of Health and Life Sciences, University of Exeter, Exeter, UK.
Jane A H Masoli *Department of Clinical and Biomedical Sciences, Faculty of Health and Life Sciences, University of Exeter, Exeter, UK.
Concepción Violán *Unitat de Suport a La Recerca Metropolitana Nord, Fundacio Institut Universitari Per a La Recerca a L'Atencio Primaria de Salut Jordi Gol I Gurina (IDIAPJGol), Barcelona, 08007, Spain.
Luke C Pilling *Department of Clinical and Biomedical Sciences, Faculty of Health and Life Sciences, University of Exeter, Exeter, UK.
Timothy M Frayling *Department of Clinical and Biomedical Sciences, Faculty of Health and Life Sciences, University of Exeter, Exeter, UK.
João Delgado *Department of Clinical and Biomedical Sciences, Faculty of Health and Life Sciences, University of Exeter, Exeter, UK.

Funding

Medical Research Council MR/W014548/1Ministerio de Ciencia e Innovación INT23/00040
6 · The paper itself

Abstract

backgroundWe previously identified genetic correlation between pairs of musculoskeletal (MSK) and respiratory conditions. Strategies to prevent or delay their onset remain underexplored in the context of multimorbidity. This study investigated whether MSK-respiratory disease pairs show evidence of potential causal relationships, identified modifiable risk factors, and quantified intervention windows to prevent progression to multimorbidity.

methodsWe examined combinations of one respiratory condition (asthma, COPD) and one MSK condition [rheumatoid arthritis (RA), osteoarthritis (OA), polymyalgia rheumatica (PMR), psoriasis]. Two-sample Mendelian randomisation (MR) evaluated potential causal relationships in both directions. Linked electronic health records from CPRD (N = 11,042,985; age ≥ 40 years) were used to assess longitudinal disease trajectories, prognostic consequences, and mediation by potentially modifiable or treatable factors.

resultsWe found evidence for bidirectional relationships between COPD and RA/OA (ORs 1.10-1.19) and between asthma and RA/OA (ORs 1.03-1.14). COPD genetic liability also increased PMR risk (OR 1.14, 95% CI 1.03-1.25). Psoriasis liability increased risk of COPD (OR 1.04, 95% CI 1.02-1.07) and asthma (OR 1.05, 95% CI 1.03-1.08). Across disease pairs, the median interval between first and second diagnoses was 5-13 years, indicating a substantial window for intervention. Obesity, smoking, hypertension, and thyroid conditions were risk factors common across all studied conditions. Mediation analyses suggested reduced physical activity and lipid changes partially contributed to the onset of respiratory disease following MSK conditions. Colocalisation identified genetic variants causal for specific condition pairs (implicating genes IFIH1, APOE, and CXCR5), highlighting inflammatory and lipid pathways.

conclusionsMSK and respiratory conditions commonly develop sequentially over many years. Targeted strategies promoting physical function, optimising lipid and cardiovascular risk management may help delay or prevent multimorbidity progression.

Indexed as

Musculoskeletal DiseasesRespiratory Tract DiseasesAdultAgedFemaleGenetic Predisposition to DiseaseHumansMaleMendelian Randomization AnalysisMiddle AgedRisk FactorsAsthmaCausal inferenceChronic obstructive pulmonary disease (COPD)Electronic health recordsMendelian randomisationMultimorbidityOsteoarthritisPolymyalgia rheumaticaRespiratory diseasesRheumatoid arthritis

Identifiers

PMID42260503
PMCPMC13573401

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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.