Short-term Effects of Tolvaptan in Individuals With Autosomal Dominant Polycystic Kidney Disease at Various Levels of Kidney Function

被引:69
作者
Boertien, Wendy E. [1 ]
Meijer, Esther [1 ]
de Jong, Paul E. [1 ]
ter Horst, Gert J. [2 ]
Renken, Remco J. [2 ]
van der Jagt, Eric J. [3 ]
Kappert, Peter [3 ]
Ouyang, John [4 ]
Engels, Gerwin E. [5 ]
van Oeveren, Willem [5 ]
Struck, Joachim [6 ]
Czerwiec, Frank S. [4 ]
Oberdhan, Dorothee [4 ]
Krasa, Holly B. [4 ]
Gansevoort, Ron T. [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Nephrol, Groningen, Netherlands
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Neurosci, Neuroimaging Ctr, Groningen, Netherlands
[3] Univ Groningen, Univ Med Ctr Groningen, Dept Radiol, Groningen, Netherlands
[4] Otsuka Pharmaceut Dev & Commercializat Inc, Rockville, MD USA
[5] Haemoscan Bv, Groningen, Netherlands
[6] AdrenoMed AG, Hennigsdorf, Germany
关键词
Autosomal dominant polycystic kidney disease (ADPKD); tolvaptan; vasopressin V-2 receptor antagonist; drug efficacy; disease progression; kidney function; glomerular filtration rate (GFR); GLOMERULAR-FILTRATION-RATE; V2 RECEPTOR ANTAGONIST; VASOPRESSIN; I-125-IOTHALAMATE; I-131-HIPPURAN; BIOMARKERS; COPEPTIN; VOLUME; MODEL;
D O I
10.1053/j.ajkd.2014.11.010
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: A recent study showed that tolvaptan, a vasopressin V-2 receptor antagonist, decreased total kidney volume (TKV) growth and estimated glomerular filtration rate (GFR) loss in autosomal dominant polycystic kidney disease (ADPKD) with creatinine clearance >= 60 mL/min. The aim of our study was to determine whether the renal hemodynamic effects and pharmacodynamic efficacy of tolvaptan in ADPKD are dependent on GFR. Study Design: Clinical trial with comparisons before and after treatment. Setting & Participants: Patients with ADPKD with a wide range of measured GFRs (mGFRs; 18-148 mL/min) in a hospital setting. Intervention: Participants were studied at baseline and after 3 weeks of treatment with tolvaptan given in increasing dosages, if tolerated (doses of 60, 90, and 120 mg/d in weeks 1, 2, and 3, respectively). Outcomes: Change in markers for aquaresis (free-water clearance, urine and plasma osmolality, 24-hour urine volume, and plasma copeptin) and kidney injury (TKV and kidney injury biomarkers). Measurements: GFR was measured by 125 I-iothalamate clearance; TKV, by magnetic resonance imaging; biomarker excretion, by enzyme-linked immunosorbent assay; and osmolality, by freezing point depression. Results: In 27 participants (52% men; aged 46 +/- 10 years; mGFR, 69 +/- 39 mL/min; TKV, 2.15 [IQR, 1.10-2.77] L), treatment with tolvaptan led to an increase in urine volume and free-water clearance and a decrease in urine osmolality, TKV, and kidney injury marker excretion. Changes in urine volume and osmolality with treatment were less in participants with lower baseline mGFRs (both P < 0.01). However, change in fractional free-water clearance was greater at lower baseline mGFRs (P = 0.001), suggesting that participants with decreased GFRs responded more to tolvaptan per functioning nephron. Limitations: Limited sample size, no control group. Conclusions: In patients with ADPKD with decreased kidney function, response to tolvaptan is lower for TKV, urinary volume, and osmolality, but larger for fractional free-water clearance. This latter finding suggests that patients with ADPKD with lower GFRs might benefit from long-term treatment with tolvaptan, as has been observed for patients with preserved GFRs. (C) 2015 by the National Kidney Foundation, Inc.
引用
收藏
页码:833 / 841
页数:9
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