Fetal programming of cardiac function and disease

Research output: Contribution to journalReview articlepeer-review

Abstract

Fetal programming describes long-term adaptive changes that an organism undergoes in response to an intrauterine insult. This term was coined to describe the increased incidence of adult disease, such as cardiovascular disease, seen among populations that suffered an intrauterine insult. While changes induced by such an insult may be initially beneficial, they can have deleterious long-term effects. Cardiac programming effects can be induced by maternal diet alterations, fetal exposure to increased levels of corticosteroids, chronic fetal hypoxia and anemia, and maternal use of nicotine or cocaine. These stimuli result in a variety of changes in cardiac function and gene expression, many of which persist into adulthood. A possible mediator of these changes is an alteration in the DNA methylation pattern of the cardiomyocytes. This review gives an overview of the changes that have been observed in the heart in response to various programming stimuli and potential programming mechanisms. © 2007 by the Society for Gynecologic Investigation.
Original languageEnglish
Pages (from-to)209-216
Number of pages8
JournalReproductive Sciences
Volume14
Issue number3
DOIs
StatePublished - Apr 2007

ASJC Scopus Subject Areas

  • Obstetrics and Gynecology

Keywords

  • Cocaine
  • DNA methylation
  • Hypoxia
  • Nutrition
  • Adrenal Cortex Hormones/adverse effects
  • Epigenesis, Genetic
  • Humans
  • Fetal Nutrition Disorders/physiopathology
  • Prenatal Exposure Delayed Effects/genetics
  • Cardiovascular Physiological Phenomena/drug effects
  • Fetal Growth Retardation/etiology
  • Pregnancy
  • Myocytes, Cardiac/physiology
  • Animals
  • DNA Methylation/drug effects
  • Female
  • Maternal Exposure/adverse effects
  • Cardiovascular Diseases/etiology

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