ArticleFrontiers in endocrinology2025
Osteoarthritis as a clinical marker of cardiovascular-kidney-metabolic multimorbidity: a population-based cohort study in China.
Article in Frontiers in endocrinology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- Systemic implications of osteoarthritis: from local degeneration to systemic metabolic Dysregulation.Journal of translational medicine · 2026Review
- Cardiovascular-kidney-metabolic syndrome: a comprehensive review of pathophysiology, epidemiology, diagnosis, and management.Cardiovascular diabetology · 2026Review
- Metabolic Dysfunction at the Core: Revisiting the Overlap of Cardiovascular, Renal, Hepatic, and Endocrine Disorders.Life (Basel, Switzerland) · 2026Review
- Osteoarthritis as a systemic disorder: multi-organ crosstalk in pathogenesis and therapeutic targeting.Frontiers in immunology · 2026Review
- Beyond cardiovascular disease: remnant cholesterol as a novel risk factor for osteoarthritis.Frontiers in nutrition · 2025Article
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5 authors.
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Abstract
Background: Cardiovascular-kidney-metabolic (CKM) multimorbidity is increasingly recognized as a major global health concern. Although osteoarthritis (OA) is traditionally viewed as a degenerative joint condition, recent evidence suggests it may reflect systemic inflammation and metabolic dysfunction. However, its role as a potential clinical marker of CKM multimorbidity remains unclear. Methods: This population-based cohort study included 1,842 participants with osteoarthritis from a community registry in China. CKM multimorbidity was defined as the sequential development of cardiovascular disease (CVD), chronic kidney disease (CKD), and type 2 diabetes mellitus (T2DM). Participants were followed for incident CKM events. Logistic regression models estimated odds ratios (ORs) for new-onset, double, and triple CKM outcomes. A multi-state model was applied to assess progression trajectories between disease stages. Results: Over the study period, 32.6% of participants developed at least one CKM condition, 27.1% progressed to double CKM, and 5.4% developed triple CKM. Higher osteoarthritis burden was associated with increased risk of CKM multimorbidity. Adjusted ORs (95% CI) for new-onset, double, and triple CKM were 2.64 (2.33 - 3.00), 2.40 (2.11 - 2.72), and 1.49 (1.21 - 1.84), respectively. Multi-state modeling confirmed that osteoarthritis. Conclusion: Osteoarthritis is strongly associated with the onset and progression of CKM multimorbidity. As a clinically observable and common condition, OA may serve as an early indicator for identifying individuals at heightened risk of multi-organ metabolic decline. These findings support the integration of OA status into risk stratification frameworks for CKM disease prevention and management.
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