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Table 5 Effect of tolvaptan 60 mg at baseline, during, and after systemic inhibition of NO synthesis on brachial systolic blood pressure (SBP), diastolic blood pressure (DBP), and pulse rate 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

Baseline

L-NMMA

Post infusion

p (GLM-within)

Prior to L-NMMA infusion

At the beginning of infusion

At the end of infusion

30 min after the end of L-NMMA infusion

60 min after the end of L-NMMA infusion

SBP (mmHG)

 Placebo

137 ± 12

146 ± 17

149 ± 16

147 ± 16

146 ± 13

0.407

 Tolvaptan 60 mg

135 ± 9

144 ± 15

144 ± 14

142 ± 15

144 ± 13

 p (GLM between)

0.305

     

 p (paired t-test, between)

0.276

0.623

0.107

0.134

0.332

 

DBP (mmHg)

 Placebo

82 ± 10

88 ± 11

90 ± 10

87 ± 9

87 ± 9

0.502

 Tolvaptan 60 mg

81 ± 8

88 ± 9

87 ± 9

85 ± 8

85 ± 8

 p (GLM between)

0.659

     

 p (paired t-test, between)

0.410

0.762

0.094

0.101

0.190

 

Pulse rate (BPM)

 Placebo

58 ± 9

55 ± 8

55 ± 9

56 ± 9

6 0 ± 10

0.319

 Tolvaptan 60 mg

58 ± 9

54 ± 9

54 ± 9

57 ± 10

60 ± 11

 p (GLM between)

0.991

     

 p (paired t-test, between)

0.699

0.431

0.502

0.873

0.966

 
  1. Data are given as mean ± SD. General linear model (GLM) with repeated measures was performed for comparison within and between treatment groups. Post-hoc Bonferoni test was used for comparison between L-NMMA infusion period (at the beginning/ at the end of L-NMMA infusion period) vs baseline (prior to L-NMMA infusion period) and baseline vs post infusion period (30 min/60 min after the end of L-NMMA infusion) vs baseline, none of the p- values were significant. Paired t-test was used for comparison between treatment groups