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Published on: March 28, 2017
Drug metabolizing enzymes in the perinatal and neonatal period: differences in the expression and activity
1Department of Public Health & Community Medicine-Section of Pharmacology, University of Verona, Policlinico G.B. Rossi, Piazzale L.A. Scuro, 37134 Verona, Italy. laura.cuzzolin@univr.it
Insights
Neonatal drug metabolism is immature, impacting treatment efficacy and toxicity. This review covers differences in drug-metabolizing enzymes and their clinical relevance in newborns.
Area of Science:
- Pharmacology
- Neonatal Medicine
- Drug Metabolism
Background:
- Physiological changes during the perinatal period and early infancy significantly influence drug response.
- Drug efficacy and toxicity exhibit high variability in the neonatal population.
- Immature drug metabolism is a key factor contributing to this variability.
Purpose of the Study:
- To review qualitative and quantitative differences in neonatal drug-metabolizing enzymes.
- To examine the immaturity of Phase I and Phase II metabolic pathways at birth.
- To discuss the maturational changes in these pathways during early extrauterine life.
Main Methods:
- Literature review of studies on drug metabolism in neonates.
- Analysis of data on Phase I and Phase II enzyme activity and expression.
- Synthesis of information on developmental changes in metabolic pathways.
Main Results:
- Both Phase I and Phase II drug metabolism pathways are immature in neonates.
- Significant maturational changes occur in these pathways in the first month of life.
- Enzyme activity and expression levels differ qualitatively and quantitatively compared to adults.
Conclusions:
- Neonatal immaturity of drug metabolism significantly affects pharmacological treatment outcomes.
- Understanding these metabolic differences is crucial for optimizing drug therapy in newborns.
- Clinical implications of altered drug metabolism in neonates warrant careful consideration.
Abstract:
Physiological changes occurring perinatally and in the first month of life can affect the answer to a pharmacological treatment and the individual response to a drug in terms of efficacy and toxicity is highly variable in the neonatal population. Among potential causes for such variability, differences in drug metabolism may have a great impact. This article aims to review qualitative and quantitative differences in drug metabolizing enzymes in neonates, since both phase I and phase II metabolic pathways are immature at birth and subject to maturational changes in the first period of extrauterine life. Moreover, clinical implications will be discussed.
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