Evaluates VPZ's effect on hepatic CYP activity, indicating minimal impact on drug metabolism.
Background:Proton pump inhibitors (PPIs) affect hepatic drug metabolism via cytochrome P450 (CYP) enzymes, but the impact of potassium-competitive acid blockers (P-CABs), such as vonoprazan (VPZ), is not fully understood.This study aimed to evaluate whether maintenance-dose VPZ influences hepatic CYP activity using the 13C-aminopyrine breath test (13C-ABT). Material/Methods:Twenty healthy subjects aged 18 years or older were recruited.Each participant underwent 13C-ABT under 2 conditions: without treatment (control) and after 8 days of 10 mg VPZ once daily.After oral administration of 100 mg 13C-aminopyrine, breath samples were collected before dosing and every 15-30 minutes for 3 hours.The delta-over-baseline (DOB) ratio, reflecting 13 CO 2 / 12 CO 2 , was measured using infrared spectroscopy. Results:Nineteen participants (median age 24 years; 10 men, 9 women) completed the study.In the control condition, DOB values increased from 15 minutes after dosing and reached a peak at 49.7 ± 35.8 minutes.The VPZ condition showed no significant differences in the DOB curve compared to the control condition (P = 0.316).The area under the DOB curve over 3 hours was comparable between conditions, with a geometric mean ratio of 1.09 (90% confidence interval 0.97-1.23).Peak values and time to peak were also similar between 2 conditions. Conclusions:Administration of 10 mg of VPZ did not significantly affect hepatic CYP activity as assessed by the 13C-ABT, suggesting that VPZ at a maintenance dose has minimal effect on hepatic drug metabolism and drug-drug interactions.
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Takahashi et al. (2026) studied this question.
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