Abstract

BackgroundTolvaptan slowed the rates of total kidney volume (TKV) growth and renal function decline over a 3-year period in patients with autosomal dominant polycystic kidney disease (ADPKD) enrolled in the Tolvaptan Efficacy and Safety in Management of Autosomal Dominant Polycystic Kidney Disease and Its Outcomes (TEMPO) 3:4 trial (NCT00428948). In this post hoc analysis of Japanese patients from TEMPO 3:4, we evaluated whether the effects of tolvaptan on TKV and on renal function are interrelated.MethodsOne hundred and forty-seven Japanese patients from TEMPO 3:4 were included in this analysis (placebo, n = 55; tolvaptan, n = 92). Tolvaptan-treated patients were stratified into the responder group (n = 37), defined as tolvaptan-treated patients with a net decrease in TKV from baseline to year 3, and the non-responder group (n = 55), defined as tolvaptan-treated patients with a net increase in TKV.ResultsMean changes during follow-up in the placebo, responder, and non-responder groups were 16.99%, − 8.33%, and 13.95%, respectively, for TKV and − 12.61, − 8.47, and − 8.58 mL/min/1.73 m2, respectively, for estimated glomerular filtration rate (eGFR). Compared with the placebo group, eGFR decline was significantly slowed in both the responder and non-responder groups (P < 0.05).ConclusionTolvaptan was effective in slowing eGFR decline, regardless of TKV response, over 3 years in patients with ADPKD in Japan. Treatment with tolvaptan may have beneficial effects on slowing of renal function decline even in patients who have not experienced a reduction in the rate of TKV growth by treatment with tolvaptan.

Highlights

  • Autosomal dominant polycystic kidney disease (ADPKD) is an inherited disease characterized by age-dependent development of multiple cysts in the kidneys, causing a gradual and irreversible expansion of kidney volume [1]

  • In the Tolvaptan Efficacy and Safety in Management of Autosomal Dominant Polycystic Kidney Disease and Its Outcomes (TEMPO) 3:4 clinical trial, a global, multicenter study that included patients from Japan, tolvaptan slowed the rates of total kidney volume (TKV) growth and renal function decline over a 3-year period compared with placebo in patients with autosomal dominant polycystic kidney disease (ADPKD) [10, 11]

  • Calculation of estimated glomerular filtration rate was performed as follows by two formulae: eGFR by the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation modified for Japanese = 0.813 (Japanese coefficient) × 141 × minimumα × maximum−1.209 × 0.993Age × 1.018 × 1.159 (κ is 0.7 for females and 0.9 for males, α is − 0.329 for females and − 0.411 for males) [15] and eGFR by the Japanese eGFR equation based on serum creatinine developed by the Japanese Society of Nephrology = 194 × serum ­creatinine−1.094 × age−0.287 and 194 × serum ­creatinine−1.094 × ­age−0.287 × 0.739 [16]

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Summary

Introduction

Autosomal dominant polycystic kidney disease (ADPKD) is an inherited disease characterized by age-dependent development of multiple cysts in the kidneys, causing a gradual and irreversible expansion of kidney volume [1]. In the Tolvaptan Efficacy and Safety in Management of Autosomal Dominant Polycystic Kidney Disease and Its Outcomes (TEMPO) 3:4 clinical trial, a global, multicenter study that included patients from Japan, tolvaptan slowed the rates of TKV growth and renal function decline over a 3-year period compared with placebo in patients with ADPKD [10, 11]. Tolvaptan slowed the rates of total kidney volume (TKV) growth and renal function decline over a 3-year period in patients with autosomal dominant polycystic kidney disease (ADPKD) enrolled in the Tolvaptan Efficacy and Safety in Management of Autosomal Dominant Polycystic Kidney Disease and Its Outcomes (TEMPO) 3:4 trial (NCT00428948). Treatment with tolvaptan may have beneficial effects on slowing of renal function decline even in patients who have not experienced a reduction in the rate of TKV growth by treatment with tolvaptan

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