Abstract
Pharmacogenomics, the study of specific genetic variations and their effect on drug response, will likely give rise to many applications in maternal–fetal and neonatal medicine; yet, an understanding of these applications in the field of obstetrics and gynecology and neonatal pediatrics is not widespread. This review describes the underpinnings of the field of pharmacogenomics and summarizes the current pharmacogenomic inquiries in relation to maternal–fetal medicine—including studies on various fetal and neonatal genetic cytochrome P450 (CYP) enzyme variants and their role in drug toxicities (for example, codeine metabolism, sepsis and selective serotonin reuptake inhibitor (SSRI) toxicity). Potential future directions, including alternative drug classification, improvements in drug efficacy and non-invasive pharmacogenomic testing, will also be explored.
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Acknowledgements
We thank Dr Brian Mercer for his insightful comments and suggestions. We also thank Dorit Berlin and her colleagues at the pharmGKB for their assistance.
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Blumenfeld, Y., Reynolds-May, M., Altman, R. et al. Maternal–fetal and neonatal pharmacogenomics: a review of current literature. J Perinatol 30, 571–579 (2010). https://doi.org/10.1038/jp.2009.183
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DOI: https://doi.org/10.1038/jp.2009.183