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Reduction in Osteoarthritis Risk After Treatment With Ticagrelor Compared to Clopidogrel: A Propensity Score-Matching
Matthew C Baker1, Yingjie Weng1, William H Robinson2
1Stanford University, Stanford, California.
Insights
Ticagrelor treatment may reduce osteoarthritis risk. This study found a 29% lower risk of developing osteoarthritis in patients treated with ticagrelor compared to clopidogrel.
Area of Science:
- Rheumatology
- Pharmacology
- Cardiology
Background:
- Osteoarthritis (OA) is a prevalent cause of joint pain and disability with limited effective treatments.
- Extracellular adenosine exhibits anti-inflammatory properties and has shown potential in preventing and treating OA in preclinical models.
- Ticagrelor, unlike clopidogrel, is known to increase extracellular adenosine levels, suggesting a potential therapeutic role in OA.
Purpose of the Study:
- To investigate the association between ticagrelor treatment and the risk of developing osteoarthritis (OA).
- To compare the incidence of OA diagnosis in patients receiving ticagrelor versus clopidogrel.
Main Methods:
- A 1:2 propensity score-matched analysis was conducted using data from 2011-2017.
- Patients treated with ticagrelor or clopidogrel for at least 90 days, without prior OA or inflammatory arthritis, were included.
- The primary outcome was the time to OA diagnosis, identified via International Classification of Diseases codes.
Main Results:
- The study included 7,007 ticagrelor-treated patients and 14,014 clopidogrel-treated patients.
- Multivariate Cox regression analysis revealed a 29% lower risk of developing OA in the ticagrelor group (Hazard Ratio: 0.71; 95% CI: 0.64-0.79; P < 0.001).
- The median treatment duration was similar between groups (287 days for ticagrelor, 284 days for clopidogrel).
Conclusions:
- Ticagrelor treatment is associated with a significantly reduced risk of developing osteoarthritis compared to clopidogrel.
- The observed protective effect of ticagrelor against OA may be partly attributed to its ability to increase extracellular adenosine levels.
- These findings suggest a potential novel therapeutic application for ticagrelor in the management or prevention of osteoarthritis.
Objective:
Osteoarthritis (OA) is a common cause of joint pain and disability, and effective treatments are lacking. Extracellular adenosine has antiinflammatory effects and can prevent and treat OA in animal models. Ticagrelor and clopidogrel are both used in patients with coronary artery disease, but only ticagrelor increases extracellular adenosine levels. This study was undertaken to determine whether treatment with ticagrelor was associated with a lower risk of OA.
Methods:
We conducted a 1:2 propensity score-matching analysis using data from 2011-2017 in the Optum Clinformatics Data Mart. Patients who had received either ticagrelor or clopidogrel for ≥90 days were included in our study, and patients with a prior diagnosis of OA or inflammatory arthritis were excluded. OA was identified using International Classification of Diseases codes. The primary outcome was the time to diagnosis of OA after treatment with ticagrelor versus clopidogrel.
Results:
Our propensity score-matched cohort consisted of 7,007 ticagrelor-treated patients and 14,014 clopidogrel-treated patients, with a median number of days receiving treatment of 287 and 284, respectively. For both groups, the mean age was 64 years, and 73% of the patients were male. Multivariate Cox regression analysis estimated a hazard ratio for developing OA of 0.71 (95% confidence interval 0.64-0.79) (P < 0.001) after treatment with ticagrelor compared to clopidogrel.
Conclusion:
Treatment with ticagrelor was associated with a 29% lower risk of developing OA compared to treatment with clopidogrel over 5 years of follow-up. We hypothesize that the reduction in OA seen in patients who received ticagrelor may in part be due to increased extracellular adenosine levels.
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