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Table 4 Effect of tolvaptan 60 mg at baseline, during and after systemic inhibition of NO synthesis on plasma concentrations of renin (PRC), angiotensin II (P-AngII) and aldosterone (P-Aldo) in a randomized, placebo-controlled, double-blind, crossover study of 18 ADPKD patients

From: Effect of tolvaptan on renal handling of water and sodium, GFR and central hemodynamics in autosomal dominant polycystic kidney disease during inhibition of the nitric oxide system: a randomized, placebo-controlled, double blind, crossover study

Periods

Prior to L-NMMA infusion period

At the end of L-NMMA infusion period

1 h after L-NMMA infusion period

P (GLM-within)

PRC(pg/ml)

 Placebo

8.8 ± 5.3

7.4 ± 4.0

7.7 ± 4.3

0.610

 Tolvaptan 60 mg

10.1 ± 5.8

8.9 ± 6.1

8.4 ± 4.9

 p (GLM between)

0.489

   

 p (paired t-test, between)

0.481

0.312

0.523

 

P-AngII (pg/ml)

 Placebo

7.8 ± 3.8

7.4 ± 3.8

7.1 ± 3.1

0.801

 Tolvaptan 60 mg

9.1 ± 5.9

8.9 ± 4.7

8.6 ± 4.3

 p (GLM between)

0.327

   

 p (paired t-test, between)

0.377

0.151

0.261

 

P- Aldo (pmol/L)

 Placebo

125 (68; 168)

127 (99; 224)

119 (87; 224)

 

 Tolvaptan 60 mg

115 (87; 180)

147 (115; 205)

178 (108; 264)

 p (Wilcoxon’s signed rank test, between)

0.420

0.433

0.170

  1. Data are given as mean ± SD or median with 25th and 75th percentiles in parentheses. General linear model (GLM) with repeated measures was performed for comparison within and between groups. Post-hoc Bonferoni test was used for comparison between L-NMMA infusion period (at the end of L-NMMA infusion period) vs baseline (prior to L-NMMA infusion period) and at baseline vs post infusion period (1 h after L-NMMA infusion period) vs baseline period, none of the p- values were significant. Paired t-test was performed to test differences between treatment groups