Cohort study reveals accelerated kidney function decline in polycystic kidney disease with baseline hematuria, indicating that urine tests complement imaging risk markers.
Background Hematuria is common in autosomal dominant polycystic kidney disease (ADPKD), but whether baseline hematuria predicts long-term kidney outcomes is unknown. We tested its association with kidney function decline, renal survival and volume growth. Methods In a single-centre ADPKD cohort, 175 patients had standardized urinary sediment assessment in a baseline period (2006–2011); 173 (99%) were linked to a registry (follow-up up to 20 years). Microscopic hematuria was > 5 erythrocytes per high-power field; macroscopic was from clinical history. Outcomes were the estimated glomerular filtration rate (eGFR) slope, a composite of end-stage kidney disease or eGFR halving, and total kidney volume (TKV) growth, adjusted for baseline eGFR, age and sex. Results Baseline hematuria was present in 45 patients (26%; microscopic 15%, macroscopic 17%) and was associated with faster adjusted eGFR decline (mixed-model differential slope: any − 1.46 ml/min/1.73 m²/year [95% confidence interval (CI), −2.12 to − 0.80]; macroscopic − 1.73 [−2.53 to − 0.93]; microscopic − 1.53 [−2.34 to − 0.73]; P < 0.001 for all). The composite end point was more frequent with hematuria (15-year event-free survival 33% versus 58%; P = 0.002); macroscopic hematuria was independently associated (adjusted hazard ratio 1.97 [1.08–3.58]; P = 0.03). Hematuria was not associated with TKV growth (all P > 0.3). Associations persisted after adjustment for baseline kidney volume and albuminuria and in never-treated patients, were dose-dependent for macroscopic hematuria, and strengthened for microscopic hematuria when infection-associated episodes were excluded. Conclusions Baseline hematuria—particularly macroscopic and non–infection-associated microscopic—independently predicts accelerated functional decline and worse renal survival. Because this prognostic signal is functional rather than volume-driven, this simple, routinely available finding may complement imaging-based risk markers.
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Serra et al. (2026) studied this question.
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