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Heart disease and the risk of allopurinol-associated severe cutaneous adverse reactions: a general population-based
Chio Yokose1, Na Lu1, Hui Xie1
1Division of Rheumatology, Allergy and Immunology (Yokose, McCormick, Choi), Massachusetts General Hospital, Boston, Mass.; Arthritis Research Canada (Lu, Xie, Li, Zheng, McCormick, Rai, Aviña-Zubieta, Choi), Richmond, BC; Faculty of Health Sciences (Xie), Simon Fraser University, Burnaby, BC; Division of Rheumatology (Aviña-Zubieta), University of British Columbia, Vancouver, BC.
Insights
Heart disease increases the risk of severe cutaneous adverse reactions to allopurinol. Lowering allopurinol dosage significantly reduces this risk, especially in patients with heart and kidney disease.
Area of Science:
- Pharmacovigilance
- Cardiology
- Dermatology
Background:
- Allopurinol is a common gout medication with potential for expanded use.
- Heart disease is a suspected risk factor for severe cutaneous adverse reactions (SCARs) to allopurinol.
Purpose of the Study:
- To confirm the association between heart disease and allopurinol-associated SCARs in a Canadian population.
- To identify risk factors and evaluate mitigation strategies for allopurinol-induced SCARs.
Main Methods:
- Population-based cohort study in British Columbia (1997-2015).
- Identified incident allopurinol users and assessed risk of SCAR hospital admissions.
- Adjusted for known risk factors and evaluated joint effects of clinical/demographic factors.
Main Results:
- 130,325 allopurinol initiators; 109 SCAR admissions.
- Heart disease associated with 1.55-fold increased SCAR risk.
- High-dose allopurinol (>100 mg/d) in patients with heart and kidney disease showed an 11-fold higher risk.
- Low-dose initiation reduced risk fivefold in this population.
- Older women with heart disease from Asian-populated regions had a 23-fold higher risk.
Conclusions:
- Heart disease is an independent risk factor for allopurinol-associated SCARs, similar to chronic kidney disease.
- Low-dose allopurinol initiation can significantly mitigate SCAR risk.
- Consideration of risk factors is crucial when prescribing allopurinol.
Background:
Allopurinol is commonly prescribed for gout, and its clinical use may expand with ongoing trials assessing its potential cardiorenal benefits. Because heart disease has been suggested to be a risk factor for allopurinol-associated severe cutaneous adverse reactions, we sought to confirm this association in a Canadian general population cohort.
Methods:
We used population data from British Columbia, Canada, to identify all incident allopurinol users between 1997 and 2015. We examined the association between heart disease (ischemic heart disease and heart failure) and the risk of hospital admission for severe cutaneous adverse reactions, adjusting for known and purported risk factors. We also evaluated the joint effects of combined clinical and demographic risk factors.
Results:
Among 130 325 allopurinol initiators, 109 hospital admissions occurred for allopurinol-associated severe cutaneous adverse reactions. The multivariable relative risk among those with heart disease was 1.55 (95% confidence interval 1.01-2.37). Patients with heart disease and chronic kidney disease who were started on an allopurinol dosage of greater than 100 mg/d had an 11-fold higher risk. Allopurinol initiation at a lower dosage among patients with heart disease and chronic kidney disease resulted in a fivefold reduction in risk. Older women with heart disease from regions with large Asian populations had a 23-fold higher risk of allopurinol-associated severe cutaneous adverse reactions than younger men without heart disease from other regions.
Interpretation:
Heart disease is independently associated with risk of allopurinol-associated severe cutaneous adverse reactions, similar to chronic kidney disease, and low-dosage allopurinol initiation may substantially mitigate this risk. Risk factors for these rare but serious reactions should be considered when initiating allopurinol.
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