Pharmacogenetics of drug-induced birth defects: what is known so far?

Pharmacogenomics. 2011 Apr;12(4):547-58. doi: 10.2217/pgs.10.201.

Abstract

A literature review was performed to collect information on the role of pharmacogenetics in six proposed teratogenic mechanisms associated with drug use during pregnancy: folate antagonism, oxidative stress, angiotensin-converting enzyme inhibition and angiotensin II receptor antagonism, cyclooxygenase-1 and -2 inhibition, 5-hydroxytryptamine-reuptake inhibition and drug transporters in the placenta. Data on the direct relationship between pharmacogenetics and drug-induced birth defects were found for folate metabolism, oxidative stress caused by phenytoin exposure and drug transporters in the placenta. Although no specific data to support pharmacogenetic-related birth defects were found for the NSAIDs, paroxetine and fluoxetine, it might be expected that polymorphisms modify their teratogenic effects. The usually low prevalence of drug-induced malformations impedes the demonstration of the contribution of pharmacogenetics. Large-scale studies, preferably case-control studies, are needed.

Publication types

  • Review

MeSH terms

  • Abnormalities, Drug-Induced / genetics*
  • Angiotensin Receptor Antagonists / adverse effects
  • Angiotensin Receptor Antagonists / therapeutic use
  • Angiotensin-Converting Enzyme Inhibitors / adverse effects
  • Angiotensin-Converting Enzyme Inhibitors / therapeutic use
  • Congenital Abnormalities / genetics*
  • Cyclooxygenase 2 Inhibitors / adverse effects
  • Cyclooxygenase 2 Inhibitors / therapeutic use
  • Female
  • Folic Acid / metabolism
  • Folic Acid Antagonists / adverse effects
  • Folic Acid Antagonists / therapeutic use
  • Genetic Association Studies
  • Humans
  • Oxidative Stress / genetics
  • Pharmacogenetics
  • Polymorphism, Single Nucleotide / genetics
  • Pregnancy
  • Serotonin 5-HT1 Receptor Antagonists / adverse effects
  • Serotonin 5-HT1 Receptor Antagonists / therapeutic use*
  • Teratogens / toxicity

Substances

  • Angiotensin Receptor Antagonists
  • Angiotensin-Converting Enzyme Inhibitors
  • Cyclooxygenase 2 Inhibitors
  • Folic Acid Antagonists
  • Serotonin 5-HT1 Receptor Antagonists
  • Teratogens
  • Folic Acid