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. 2008 Feb 20;65(5):767–774. doi: 10.1111/j.1365-2125.2008.03104.x

Table 2.

Pharmacokinetic parameters of omeprazole, 5-hydroxyomeprazole and the sulphone metabolite after a single oral 40-mg dose of omeprazole to 16 healthy volunteers

Units CYP2C19*1/*1 Mean (95% CI) CYP2C19*17/*17 Mean (95% CI) P-value
Omeprazole
 AUC nmol h l−1 4151 (2084, 6218) 1973 (1476, 2469) 0.04*
 CL l h−1 48 (22, 75) 61 (44, 77) 0.37
Tmax h 2.1 (1.2, 3.1) 2.1 (1.1, 3.1) 0.95
Cmax nmol l−1 2109 (1169, 3049) 1447 (1069, 1825) 0.16
 λΖt1/2 h 1.2 (0.9, 1.5) 0.9 (0.6, 1.2) 0.18
5-Hydroxyomeprazole
 AUC nmol h l−1 3359 (2803, 3915) 2989 (2273, 3706) 0.33
Tmax h 2.4 (1.2, 3.7) 2.1 (1.1, 3.1) 0.65
Cmax nmol l−1 1534 (1081, 1988) 1527 (1234, 1819) 0.97
 λΖt1/2 h 1.3 (0.9, 1.6) 1.1 (1.0, 1.3) 0.33
Omeprazole sulphone
 AUC nmol h l−1 3343 (1301, 5384) 1083 (690, 1476) 0.03*
Tmax h 2.6 (1.4, 3.8) 2.2 (1.3, 3.1) 0.54
Cmax nmol l−1 563 (362, 765) 336 (239, 433) 0.04*
 λΖt1/2 h 3.3 (1.7, 4.8) 1.9 (1.4, 2.4) 0.09
OME AUC/5-OH AUC 1.2 (0.70, 1.6) 0.66 (0.54, 0.79) 0.04*

The lack of statistical significance, despite significant differences in AUC values, is due to the transformation of AUC values inherent in the calculation of clearance, CL = dose

*

(1/AUC). CYP2C19*17/*17 (n = 5) and CYP2C19*1/*1 (n = 11) groups were compared with an unpaired two-tailed heteroscedastic t-test. Asterisks denote P-values < 0.05. Values are means with 95% confidence interval in parentheses.