Application of pharmacogenomic strategies to the study of drug-induced birth defects
1Department of Pediatrics, Section of Developmental Pharmacology and Experimental Therapeutics, Children's Mercy Hospitals and Clinics, Kansas city, Missouri, USA. sleeder@cmh.edu
Insights
Major birth defects affect 3% of US infants annually, causing over 21% of infant deaths. Future research in pharmacogenomics may help understand congenital malformations and individual susceptibility.
Area of Science:
- Pediatric Medicine
- Genetics
- Public Health
Background:
- Major birth defects impact approximately 3% of infants, leading to over 150,000 affected births yearly in the U.S.
- Birth defects are the primary cause of infant mortality, accounting for more than 21% of all infant deaths.
- The causes and factors influencing susceptibility to most congenital malformations remain largely unknown.
Purpose of the Study:
- To highlight the significant public health burden of major birth defects.
- To underscore the current limitations in understanding the etiology and determinants of congenital malformations.
- To introduce pharmacogenomic analyses as a promising future research direction.
Main Methods:
- This abstract does not detail specific methods but points to the need for future research.
- It emphasizes the potential of pharmacogenomic analyses.
- The focus is on the problem statement and future research avenues.
Main Results:
- The abstract does not present specific results but outlines the scope of the problem.
- It indicates that over 150,000 infants are affected by major birth defects annually in the U.S.
- Birth defects represent the leading cause of infant mortality.
Conclusions:
- Major birth defects pose a substantial threat to infant health and survival.
- Current understanding of the causes of congenital malformations is limited.
- Pharmacogenomic analyses hold promise for advancing the understanding and potential prevention of birth defects.
Abstract:
Approximately 3% of all infants are born with one or more major birth defects, resulting in >150,000 affected babies each year in the US alone. At present, birth defects account for more than 21% of all infant deaths, making them the leading cause of infant mortality. Although the etiology and determinants of individual susceptibility are largely unknown for most congenital malformations, pharmacogenomic analyses offer promise for the future.
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