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Effect of Allopurinol Use on Kidney Function Among Patients with Gout and Chronic Kidney Disease
Ana Beatriz Vargas-Santos1, Christine E Peloquin2, Tuhina Neogi2
1Rheumatology Unit, Hospital Universitário Pedro Ernesto, Universidade do Estado do Rio de Janeiro, Rio de Janeiro 20551-030, RJ, Brazil.
Insights
Allopurinol use in patients with gout and chronic kidney disease (CKD) did not worsen renal function. This study suggests allopurinol may even slightly improve kidney function in CKD patients with gout.
Area of Science:
- Nephrology
- Rheumatology
- Pharmacology
Background:
- Conflicting evidence exists on allopurinol's renal effects in gout patients.
- Clinicians often hesitate to prescribe allopurinol to patients with chronic kidney disease (CKD).
Purpose of the Study:
- To investigate the association between allopurinol use and renal function changes in patients with gout and CKD stages 3-4.
- To determine if allopurinol is detrimental to kidney function in this population.
Main Methods:
- A time-stratified propensity score (PS)-matched cohort study was conducted using UK general population data.
- 10,716 new allopurinol users with gout and CKD 3-4 were matched 1:1 with non-users.
- Changes in estimated glomerular filtration rate (eGFR) at one year were analyzed using adjusted linear regression.
Main Results:
- Allopurinol initiators showed a mean eGFR increase of 0.81 mL/min compared to non-users.
- The progression to dialysis or kidney transplant was similar between the allopurinol and non-user groups.
- No evidence of allopurinol worsening renal function was observed.
Conclusions:
- Allopurinol use in patients with gout and CKD stages 3-4 is not associated with worsening renal function.
- Allopurinol may have a slight beneficial effect on renal function in this patient group.
- The findings suggest allopurinol can be safely used in patients with gout and CKD.
Abstract:
The evidence regarding allopurinol's effects on renal function among people with hyperuricemia and gout has been conflicting, though clinicians are often cautious about using allopurinol in chronic kidney disease (CKD). We sought to examine the relation between allopurinol use in those with gout and CKD and the risk of worsening renal function. We conducted a time-stratified propensity score (PS)-matched cohort study on the IQVIA Medical Research Data representative of the UK general population. Among participants 18-89 years old with gout and CKD 3-4 not on urate-lowering therapy within one year prior, we identified new users of allopurinol and matched them 1:1 with a non-user. We analyzed the relation between incident allopurinol use and the changes in the eGFR at one year of follow-up using linear regression adjusted for the potential confounders included in the PS model. We PS-matched 10,716 allopurinol initiators to 10,716 non-users, among whom 42% were female, the mean age was 74 years and 7% had CKD4. The progression to dialysis or kidney transplant was similar in both groups. The mean eGFR prior to the study entry was 48.4 mL/min among allopurinol initiators and 49.5 mL/min among non-users, while the last eGFR within one year was 49.4 and 49.7 mL/min, respectively. The allopurinol initiators had an adjusted mean increase in the eGFR of 0.81 mL/min (95% CI 0.57-1.05) greater than that of non-users. Among those with gout and CKD 3-4, allopurinol did not worsen renal function and may have slightly improved it, suggesting that allopurinol is not detrimental to patients with gout who have CKD.
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