TY - JOUR
T1 - Fetal programming of cardiac function and disease
AU - Meyer, Kurt
AU - Zhang, Lubo
N1 - 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.
PY - 2007/4
Y1 - 2007/4
N2 - 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.
AB - 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.
KW - Cocaine
KW - DNA methylation
KW - Hypoxia
KW - Nutrition
KW - Adrenal Cortex Hormones/adverse effects
KW - Epigenesis, Genetic
KW - Humans
KW - Fetal Nutrition Disorders/physiopathology
KW - Prenatal Exposure Delayed Effects/genetics
KW - Cardiovascular Physiological Phenomena/drug effects
KW - Fetal Growth Retardation/etiology
KW - Pregnancy
KW - Myocytes, Cardiac/physiology
KW - Animals
KW - DNA Methylation/drug effects
KW - Female
KW - Maternal Exposure/adverse effects
KW - Cardiovascular Diseases/etiology
UR - http://www.scopus.com/inward/record.url?scp=35348883813&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=35348883813&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/6e0fac79-0d7b-3adc-92bd-f074cd0577ef/
U2 - 10.1177/1933719107302324
DO - 10.1177/1933719107302324
M3 - Review article
C2 - 17636233
SN - 1933-7191
VL - 14
SP - 209
EP - 216
JO - Reproductive Sciences
JF - Reproductive Sciences
IS - 3
ER -