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A treat-to-target approach for gout confers renoprotective effect in patients with chronic kidney disease stage 3
Marta Novella-Navarro1,2, Jose Luis Cabrera-Alarcon3, Cesar Diaz-Torne4,2
1Rheumatology Department, Hospital Universitario Torrejon de Ardoz, Madrid, Spain.
Insights
Treating gout with xanthine oxidase inhibitors (XOIs) using a treat-to-target (T2T) approach improved estimated glomerular filtration rate (eGFR) in patients with chronic kidney disease (CKD). This strategy effectively lowered serum uric acid (sUA) and preserved kidney function over 12 months.
Area of Science:
- Nephrology
- Rheumatology
- Pharmacology
Background:
- Gout and chronic kidney disease (CKD) frequently coexist, posing significant management challenges.
- Serum uric acid (sUA) reduction is crucial for managing gout and potentially slowing CKD progression.
- The "treat-to-target" (T2T) strategy aims for specific sUA levels, but its impact on eGFR in CKD patients requires further investigation.
Purpose of the Study:
- To evaluate the effect of a T2T approach for gout on estimated glomerular filtration rate (eGFR) in patients with CKD stage 3.
- To assess the correlation between serum uric acid (sUA) reduction and changes in eGFR.
- To determine the efficacy of xanthine oxidase inhibitors (XOIs) in achieving sUA targets and improving renal function.
Main Methods:
- A multicenter, observational, retrospective study involving 50 patients with gout and CKD stage 3.
- Patients received xanthine oxidase inhibitors (allopurinol or febuxostat) for at least 12 months.
- Treatment followed a T2T strategy targeting sUA levels <5-6 mg/dl within 6 months, analyzed using a linear mixed-effects model.
Main Results:
- 82% of patients achieved the target sUA levels within the study period.
- A significant median increase in eGFR of 7.54 ml/min/m² was observed in the first 6 months, stabilizing thereafter.
- Each 1 mg/dl decrease in sUA correlated with a 1.58 ml/min/m² improvement in eGFR (p < 0.001).
Conclusions:
- A T2T approach using XOIs effectively reduces sUA levels in gout patients with CKD stage 3.
- This strategy demonstrates a capacity to conserve and improve renal function, evidenced by eGFR increases.
- The findings support optimizing XOI therapy within a T2T framework for managing renal outcomes in this patient population.
Abstract:
The aim of this study was to assess changes in the estimated glomerular filtration rate (eGFR) in gouty patients with chronic kidney disease (CKD) using a "treat-to-target" (T2T) approach in gout. This multicenter observational retrospective study included patients diagnosed with gout and CKD stage 3 taking xanthine oxidase inhibitors (XOIs) (allopurinol or febuxostat) for at least 12 months. All patients were treated using a T2T strategy according to national gout guidelines to achieve the target levels of serum uric acid (sUA; < 5-6 mg/dl) within 6 months of the first visit. The primary outcome was to assess changes in eGFR. The effects of independent variables were analyzed over eGFR in a linear mixed-effects (LME) model. Fifty patients with gout and CKD stage 3 treated with XOIs with a T2T strategy for 12 months were included. Eighty-two percent of the patients achieved the sUA target during the study period. The improvement seen in eGFR was higher during the first 6 months, showing a median increase of 7.54 ml/min/m2 (SE = 1.25) and trending towards stability over 12 months. For every 1 mg/dl of decrease in sUA, an improvement of 1.5 ml/min/m2 in eGFR was observed (coefficient ± SE: - 1.58 ± 0.26) (p < 0.001) with no differences between type and dosage of XOIs treatment, colchicine administration, age, sex, and smoking status. A reduction in sUA levels using a T2T approach with XOIs at an optimal dose is possible and could help conserve and improve renal function in gouty patients with CKD stage 3.
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