Autosomal dominant polycystic kidney disease (ADPKD) is the leading monogenic cause of end-stage kidney disease (ESKD). Because disease-modifying therapy is costly and can cause adverse effects, identifying patients most likely to benefit is essential. We developed and internally validated a model to predict ESKD by age 80 in class 1 ADPKD, hypothesizing that combining baseline eGFR with an exponential estimate of kidney growth would improve forecasting. We retrospectively analyzed 142 adults with class 1 ADPKD followed at a tertiary center in Mexico City (2012–2023). Total kidney volume (TKV) was measured by the ellipsoid method and eGFR by CKD-EPI 2021. Data were split 50/50 into derivation and validation sets. Future eGFR was modeled using baseline eGFR plus an exponential TKV growth surrogate; ESKD risk (eGFR <15 ml/min/1.73 m 2 ) was derived from the standard normal cumulative distribution. Performance was compared with the Mayo Clinic Predictive Model (MCPM) and a Cox model. In validation, the model achieved adjusted R 2 = 0.858 (vs. 0.830 for MCPM). ESKD prediction showed excellent discrimination (C-index = 0.94) and calibration, comparable to Cox (C-index = 0.95). This approach supports individualized lifetime ESKD risk prediction in class 1 ADPKD to guide targeted therapy and resource allocation.
Aguilar-Lugo-Gerez et al. (Sun,) studied this question.