Diminished Mycophenolic Acid Exposure Caused by Omeprazole May Be Clinically Relevant in the First Week Posttransplantation


Autoria(s): David-Neto, Elias; Takaki, Kelly M.; Agena, Fabiana; Romano, Paschoalina; Sumita, Nairo M.; Mendes, Maria E.; Lopes Neri, Leticia Aparecida; Nahas, William C.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

05/11/2013

05/11/2013

2012

Resumo

Background: Some studies have reported a decreased absorption of mycophenolic acid (MPA) from mycophenolate mofetil (MMF) in renal transplanted (RTx) patients under proton-pump inhibitors (PPIs). There is still a lack of information regarding (1) whether this effect occurs when MMF is administered with either tacrolimus or cyclosporine A [calcineurin inhibitors (CNIs)], (2) whether the effect has the same amplitude during the first year after RTx, and finally (3) whether this decrease in exposure is clinically relevant. Methods: We retrospectively analyzed the omeprazole effect in 348 12-hour pharmacokinetic samplings [area under the curve (AUC) 0-12h] performed on days 7, 14, 30, 60, 180, and 360 after RTx in 77 patients who participated in previous trials. Results: For all periods, the groups with and without PPI did not differ in all variables. By mixed-model analysis of variance, PPI reduced the MPA AUC(0-12h) (P < 0.0008) in the patients under both CNIs mainly due to decreased absorption (P = 0.049). In the tacrolimus group, a lower exposure seemed also due to a decreased MPA reabsorption at 10-12 hours. The PPI effect remains throughout the first year but was clinically more important on day 7. By Cox analysis, the use of PPI was associated with a 25% less chance of being adequately exposed to MPA (95% confidence interval 0.58-0.99, P = 0.04). Similarly, the number of patients underexposed to MPA (AUC < 30 ng.h/mL) was higher at most periods in the PPI group but again not statistically significant. Conclusions: These data indicate that PPI decreases the MPA exposure when associated with both CNIs but particularly in the first week after RTx. In this period, the MMF dose should be increased. This effect lasts throughout the first year but does not seem to be clinically relevant after the first week.

Novartis

Novartis

Pfizer

Pfizer

BristolMeirsSquibb

Bristol-Meirs-Squibb

Identificador

THERAPEUTIC DRUG MONITORING, PHILADELPHIA, v. 34, n. 3, supl., Part 3, pp. 331-336, JUN, 2012

0163-4356

http://www.producao.usp.br/handle/BDPI/41873

10.1097/FTD.0b013e31824d6e8e

http://dx.doi.org/10.1097/FTD.0b013e31824d6e8e

Idioma(s)

eng

Publicador

LIPPINCOTT WILLIAMS & WILKINS

PHILADELPHIA

Relação

THERAPEUTIC DRUG MONITORING

Direitos

closedAccess

Copyright LIPPINCOTT WILLIAMS & WILKINS

Palavras-Chave #RENAL TRANSPLANTATION #MYCOPHENOLIC ACID #PHARMACOKINETIC #PROTON-PUMP INHIBITOR #IMMUNOSUPPRESSION #PROTON PUMP INHIBITORS #HEART-TRANSPLANT RECIPIENTS #RENAL-TRANSPLANTATION #KIDNEY-TRANSPLANTATION #DRUG EXPOSURE #MOFETIL #CYCLOSPORINE #TRIAL #MEDICAL LABORATORY TECHNOLOGY #PHARMACOLOGY & PHARMACY #TOXICOLOGY
Tipo

article

original article

publishedVersion