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Increased risk of stroke in patients with osteoarthritis: a population-based cohort study

Summary Objectives Osteoarthritis (OA) is related to carotid atherosclerosis. Few studies have investigated the incidence of cerebrovascular diseases in patients with OA. Therefore, we conducted a population-based cohort study to determine the incidence and risk of stroke in patients with OA. Method...

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Published in:Osteoarthritis and cartilage 2017-07, Vol.25 (7), p.1026-1031
Main Authors: Hsu, P.-S, Lin, H.-H, Li, C.-R, Chung, W.-S
Format: Article
Language:English
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Summary:Summary Objectives Osteoarthritis (OA) is related to carotid atherosclerosis. Few studies have investigated the incidence of cerebrovascular diseases in patients with OA. Therefore, we conducted a population-based cohort study to determine the incidence and risk of stroke in patients with OA. Methods We used data from Taiwan's Longitudinal Health Insurance Database 2000 (LHID2000) to investigate the incidence of stroke in 43,635 patients with OA newly diagnosed between 2002 and 2003. The non-osteoarthritis (non-OA) cohort comprised 43,635 people from the general population. The follow-up period was from the index date of OA to the date of censoring date or stroke diagnosis, or to the end of 2010. Results The overall incidence of stroke was 36% higher in the OA cohort than in the non-OA cohort, with an adjusted hazard ratio (aHR) of 1.10 (95% confidence interval [CI] = 1.06–1.14) after adjustment for covariates. Men, age, comorbidity, non-selective nonsteroidal anti-inflammatory drugs (NSAIDs), and Cox-2 selective NSAIDs are independent risk factors of stroke. The OA adults with mild to moderate OA (aHR = 1.97, 95% CI = 1.70–2.28 for young adults; aHR = 1.33, 95% CI = 1.25–1.42 for middle-aged adults; aHR = 1.16, 95% CI = 1.12–1.21 for older adults) and severe OA (aHR = 3.78, 95% CI = 2.50–5.70 for young adults; aHR = 1.34, 95% CI = 1.16–1.56 for middle-aged adults; and aHR = 1.01, 95% CI = 0.92–1.10 for older adults) exhibited increased risks of stroke compared with their counterparts without OA. Conclusion OA may be associated with a slightly increased risk of stroke.
ISSN:1063-4584
1522-9653
DOI:10.1016/j.joca.2016.10.027