Abstract: FR-PO0264
Proteinuria Modifies the Association Between Serum Uric Acid and Subsequent Decline in eGFR: Community-Based Cohort
Session Information
- CKD: Omics, Systemic Stressors, and Targeted Pharmacotherapy
October 23, 2026 | Location: Exhibit Hall A, Convention Center
Abstract Time: 10:00 AM - 12:00 PM
Category: CKD (Non-Dialysis)
- 2201 CKD (Non-Dialysis): Epidemiology, Risk Factors, and Prevention
Authors
- Noda, Seiya, Iwate Ika Daigaku, Shiwa District, Iwate Prefecture, Japan
- Tanaka, Fumitaka, Nara Kyoiku Daigaku, Nara, Nara Prefecture, Japan
- Kikuchi, Yawara, Iwate Ika Daigaku, Shiwa District, Iwate Prefecture, Japan
- Kawashima, Eri, Iwate Ika Daigaku, Shiwa District, Iwate Prefecture, Japan
- Yoshikawa, Kazuhiro, Iwate Ika Daigaku, Shiwa District, Iwate Prefecture, Japan
- Shimoda, Haruki, Iwate Ika Daigaku, Shiwa District, Iwate Prefecture, Japan
- Sakata, Kiyomi, Iwate Ika Daigaku, Shiwa District, Iwate Prefecture, Japan
- Asahi, Koichi, Iwate Ika Daigaku, Shiwa District, Iwate Prefecture, Japan
Background
Hyperuricemia and proteinuria are independent risk factors for kidney function decline, but whether proteinuria modifies the association between serum uric acid (SUA) and renal decline is unclear.
Methods
We studied 8,266 adults aged ≥20 years in a Japanese community cohort after excluding participants with prior cardiovascular disease, gout, urate-lowering therapy, and no follow-up eGFR measurements. Proteinuria was defined as trace or greater by dipstick at baseline. Annual eGFR slope was analyzed using linear mixed-effects models with random intercepts and slopes. SUA was modeled with restricted cubic splines and multivariable adjustment. Prespecified subgroup analyses were performed by age, sex, BMI, blood pressure, diabetes, and baseline eGFR.
Results
Mean age was 61.7±13.6 years, 64% were women, mean SUA was 5.1±1.4 mg/dL, mean baseline eGFR was 78.0±12.2 mL/min/1.73 m2, and 371 participants (4.5%) had proteinuria. Mean follow-up was 7.1±2.6 years. In participants without proteinuria, eGFR slope was nearly unchanged across SUA levels (-1.11 [95% CI -1.18, -1.05] mL/min/1.73 m2/year; P=0.220). In those with proteinuria, eGFR slope showed a non-linear association with SUA, with the slowest decline at 5.0 mg/dL (-1.27 [95% CI -1.42, -1.11]) and steeper decline thereafter, reaching -2.04 [95% CI -2.24, -1.82] mL/min/1.73 m2/year at 7.8 mg/dL (P<0.001). Interaction was significant (P<0.001). In subgroup analyses, only baseline eGFR significantly modified this association after Bonferroni correction. Among participants with baseline eGFR <60 mL/min/1.73 m2, eGFR decline was consistently steeper in those with proteinuria across SUA levels. Sensitivity analysis using proteinuria ≥1+ showed a similar pattern.
Conclusion
Higher SUA was associated with faster subsequent eGFR decline in those with baseline proteinuria, but not in those without.
Funding
- Government Support – Non-U.S.