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Cardiovascular Risks of Probenecid Versus Allopurinol in Older Patients With Gout
Seoyoung C Kim1, Tuhina Neogi2, Eun Ha Kang3
1Division of Pharmacoepidemiology and Pharmacoeconomics, Brigham and Women's Hospital, Boston, Massachusetts; Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Boston, Massachusetts.
Insights
Probenecid may offer improved cardiovascular safety for gout patients compared to allopurinol. This study found a reduced risk of myocardial infarction (MI), stroke, and heart failure (HF) events with probenecid.
Area of Science:
- Cardiology
- Rheumatology
- Pharmacology
Background:
- Gout patients face elevated risks of cardiovascular (CV) diseases, including myocardial infarction (MI), stroke, and heart failure (HF).
- Understanding the comparative CV safety of different gout treatments is crucial for patient management.
Purpose of the Study:
- To compare the cardiovascular safety of probenecid versus allopurinol in patients diagnosed with gout.
- To assess the incidence of major adverse CV events and mortality associated with these two common gout medications.
Main Methods:
- A retrospective cohort study analyzed Medicare data (2008-2013) of gout patients aged 65+ initiating probenecid or allopurinol.
- Propensity score matching (1:3 ratio) created comparable cohorts. The primary outcome was a composite of MI or stroke hospitalization.
- Secondary outcomes included individual MI, stroke, coronary revascularization, HF, and mortality events.
Main Results:
- The study included 9,722 probenecid initiators matched with 29,166 allopurinol initiators.
- The primary composite endpoint (MI or stroke) occurred at a rate of 2.36 per 100 person-years for probenecid versus 2.83 for allopurinol (Hazard Ratio: 0.80; 95% CI: 0.69-0.93).
- Probenecid was associated with significantly lower risks of MI, stroke, HF exacerbation, and mortality compared to allopurinol.
Conclusions:
- In elderly gout patients, probenecid treatment demonstrated a modest reduction in the risk of cardiovascular events, including MI, stroke, and HF exacerbation, when compared to allopurinol.
- These findings suggest a potentially favorable CV safety profile for probenecid in this patient population.
Background:
Patients with gout are at an increased risk of cardiovascular (CV) disease including myocardial infarction (MI), stroke, and heart failure (HF).
Objectives:
The authors conducted a cohort study to examine comparative CV safety of the 2 gout treatments-probenecid and allopurinol-in patients with gout.
Methods:
Among gout patients ≥65 years of age and enrolled in Medicare (2008 to 2013), those who initiated probenecid or allopurinol were identified. The primary outcome was a composite CV endpoint of hospitalization for MI or stroke. MI, stroke, coronary revascularization, HF, and mortality were assessed separately as secondary outcomes. The authors estimated the incidence rate and hazard ratio of the primary and secondary outcomes in the 1:3 propensity score-matched cohort of probenecid and allopurinol initiators.
Results:
A total of 9,722 probenecid initiators propensity score-matched to 29,166 allopurinol initiators with mean age of 76 ± 7 years, and 54% males were included. The incidence rate of the primary composite endpoint of MI or stroke per 100 person-years was 2.36 in probenecid and 2.83 in allopurinol initiators with a hazard ratio of 0.80 (95% confidence interval: 0.69 to 0.93). In the secondary analyses, probenecid was associated with a decreased risk of MI, stroke, HF exacerbation, and mortality versus allopurinol. These results were consistent in the subgroup analyses of patients without baseline CV disease or those without baseline chronic kidney disease.
Conclusions:
In this large cohort of 38,888 elderly gout patients, treatment with probenecid appears to be associated with a modestly decreased risk of CV events including MI, stroke, and HF exacerbation compared with allopurinol.
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