Casteleijn Niek F, Messchendorp A Lianne, Bae Kyong T, Higashihara Eiji, Kappert Peter, Torres Vicente, Meijer Esther, Leliveld Anna M
Department of Nephrology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Expertise Center for Polycystic Kidney Disease, Groningen, The Netherlands.
Clin Exp Nephrol. 2017 Jun;21(3):375-382. doi: 10.1007/s10157-016-1297-1. Epub 2016 Jun 23.
Tolvaptan, a vasopressin V2 receptor antagonist, has been shown to reduce the rates of growth in total kidney volume (TKV) and renal function loss in ADPKD patients, but also leads to polyuria because of its aquaretic effect. Prolonged polyuria can result in ureter dilatation with consequently renal function loss. Therefore, we aimed to investigate the effect of tolvaptan-induced polyuria on ureter diameter in ADPKD patients.
70 ADPKD patients were included (51 were randomized to tolvaptan and 19 to placebo). At baseline and after 3 years of treatment renal function was measured (mGFR) and MRI was performed to measure TKV and ureter diameter at the levels of renal pelvis and fifth lumbar vertebral body (L5).
In these patients [65.7 % male, age 41 ± 9 years, mGFR 74 ± 27 mL/min/1.73 m and TKV 1.92 (1.27-2.67) L], no differences were found between tolvaptan and placebo-treated patients in 24-h urine volume at baseline (2.5 vs. 2.5 L, p = 0.8), nor in ureter diameter at renal pelvis and L5 (4.0 vs. 4.2 mm, p = 0.4 and 3.0 vs. 3.1 mm, p = 0.3). After 3 years of treatment 24-h urine volume was higher in tolvaptan-treated patients when compared to placebo (4.7 vs. 2.3 L, p < 0.001), but no differences were found in ureter diameter between both groups (renal pelvis: 4.2 vs. 4.4 mm, p = 0.4 and L5: 3.1 vs. 3.3 mm, p = 0.4).
Tolvaptan-induced polyuria did not lead to an increase in ureter diameter, suggesting that tolvaptan is a safe therapy from a urological point of view.
托伐普坦是一种血管加压素V2受体拮抗剂,已被证明可降低常染色体显性多囊肾病(ADPKD)患者的总肾体积(TKV)增长率和肾功能丧失率,但因其利水作用也会导致多尿。长期多尿可导致输尿管扩张,进而导致肾功能丧失。因此,我们旨在研究托伐普坦诱导的多尿对ADPKD患者输尿管直径的影响。
纳入70例ADPKD患者(51例随机接受托伐普坦治疗,19例接受安慰剂治疗)。在基线和治疗3年后测量肾功能(估算肾小球滤过率[mGFR]),并进行磁共振成像(MRI)以测量肾盂和第五腰椎(L5)水平的TKV和输尿管直径。
在这些患者中(男性占65.7%,年龄41±9岁,mGFR为74±27 mL/min/1.73 m²,TKV为1.92[1.27 - 2.67]L),托伐普坦组和安慰剂组患者在基线时的24小时尿量(2.5对2.5 L,p = 0.8)以及肾盂和L5水平的输尿管直径(4.0对4.2 mm,p = 0.4;3.0对3.1 mm,p = 0.3)均无差异。治疗3年后,托伐普坦治疗组患者的24小时尿量高于安慰剂组(4.7对2.3 L,p < 0.001),但两组之间的输尿管直径无差异(肾盂:4.2对4.4 mm,p = 0.4;L5:3.1对3.3 mm,p = 0.4)。
托伐普坦诱导的多尿并未导致输尿管直径增加,这表明从泌尿外科角度来看,托伐普坦是一种安全的治疗方法。