共 102 条
Pharmacogenomic testing: the case for CYP2C19 proton pump inhibitor gene-drug pairs
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作者:

Lima, John J.
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机构:
Nemours Childrens Clin, Ctr Pharmacogen & Translat Res, Jacksonville, FL 32207 USA Nemours Childrens Clin, Ctr Pharmacogen & Translat Res, Jacksonville, FL 32207 USA

Franciosi, James P.
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机构:
Nemours Childrens Hosp, Orlando, FL 32827 USA Nemours Childrens Clin, Ctr Pharmacogen & Translat Res, Jacksonville, FL 32207 USA
机构:
[1] Nemours Childrens Clin, Ctr Pharmacogen & Translat Res, Jacksonville, FL 32207 USA
[2] Nemours Childrens Hosp, Orlando, FL 32827 USA
关键词:
adverse events;
CYP2C19;
gene;
infection;
pharmacogenomic;
proton pump inhibitors;
testing;
GASTROESOPHAGEAL-REFLUX DISEASE;
COMMUNITY-ACQUIRED PNEUMONIA;
GASTRIC-ACIDITY INHIBITORS;
BACTERIAL OVERGROWTH;
RISK-FACTOR;
LANSOPRAZOLE;
PHARMACOKINETICS;
CHILDREN;
ESOMEPRAZOLE;
OMEPRAZOLE;
D O I:
10.2217/PGS.14.103
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
The use of proton pump inhibitors (PPIs) in the treatment of gastroesophageal reflux and related diseases is increasing, especially in the pediatric population. Prolonged use of PPIs has been associated with several adverse effects, including potentially life-threatening gastric and respiratory infections, which are related to dose or to the degree of gastric acid suppression. Genetic variation in the CYP2C19 gene gives rise to poor and extensive metabolizer phenotypes, which influence PPI clearance, efficacy and exposure. A recent paper linked lansoprazole-associated respiratory infections in children with the poor metabolizer phenotype. The case is made for implementing pharmacogenomic testing for the CYP2C19-PPI gene-drug pair and to dose accordingly in order to minimize PPI-associated infections.
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页码:1405 / 1416
页数:12
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