Temporal relationship between osteoarthritis and comorbidities: a combined case control and cohort study in the UK primary care setting

Author:

Swain Subhashisa12ORCID,Coupland Carol3,Mallen Christian4,Kuo Chang Fu5,Sarmanova Aliya6ORCID,Bierma-Zeinstra Sita M A7,Englund Martin8,Prieto-Alhambra Daniel9,Doherty Michael12,Zhang Weiya12

Affiliation:

1. Academic Rheumatology, Division of Rheumatology, Orthopaedics and Dermatology

2. Pain Centre and Versus Arthritis, University of Nottingham, Nottingham, UK

3. Division of Primary Care, School of Medicine, University of Nottingham, Nottingham

4. School of Medicine, Keele University, Keele, UK

5. Division of Rheumatology, Allergy and Immunology, Chang Gung Memorial Hospital, Taoyuan City, Taiwan

6. Musculoskeletal Research Unit, Bristol Medical School, Translational Health Sciences, University of Bristol, Bristol, UK

7. Department of General Practice, Department of Orthopaedic Surgery, Erasmus University Medical Center, Rotterdam, The Netherlands

8. Clinical Epidemiology Unit, Orthopaedics, Department of Clinical Sciences, Lund University, Lund, Sweden

9. Centre for Statistics in Medicine, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford

Abstract

Abstract Objective To determine the burden of comorbidities in OA and their temporal relationships in the UK. Methods The Clinical Practice Research Datalink (CPRD) GOLD was used to identify people with incident OA and age, gender and practice matched non-OA controls from UK primary care. Controls were assigned the same index date as matched cases (date of OA diagnosis). Associations between OA and 49 individual comorbidities and multimorbidities (two or more comorbidities excluding OA) both before and after OA diagnosis were estimated, adjusting for covariates, using odds ratios (aORs) and hazard ratios (aHRs), respectively. Results During 1997–2017, we identified 221 807 incident OA cases and 221 807 matched controls. Of 49 comorbidities examined, 38 were associated with OA both prior to and following the diagnosis of OA and 2 (dementia and systemic lupus erythematosus) were associated with OA only following the diagnosis of OA. People with OA had a higher risk of developing heart failure [aHR 1.63 (95% CI 1.56, 1.71)], dementia [aHR 1.62 (95% CI 1.56, 1.68)], liver diseases [aHR 1.51 (95% CI 1.37, 1.67)], irritable bowel syndrome [aHR 1.51 (95% CI 1.45, 1.58)], gastrointestinal bleeding [aHR 1.49 (95% CI 1.39, 1.59)], 10 musculoskeletal conditions and 25 other conditions following OA diagnosis. The aOR for multimorbidity prior to the index date was 1.71 (95% CI 1.69, 1.74), whereas the aHR for multimorbidity after the index date was 1.29 (95% CI 1.28, 1.30). Conclusions People with OA are more likely to have other chronic conditions both before and after the OA diagnosis. Further study on shared aetiology and causality of these associations is needed.

Funder

Versus Arthritis

University of Nottingham Vice-Chancellor Scholarship and a Beijing Joint Care Foundation Scholarship

National Institute for Health Research (NIHR) Research Professorship

NIHR Applied Research Collaboration West Midlands and the NIHR School for Primary Care Research

Foundation for Research in Rheumatology

National Health Service, the NIHR or the Department of Health and Social Care

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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