Key result
Prenatal exposure to smoking and alcohol altered infant autonomic function, reducing heart rate variability and blunting heart rate responses to tilt compared to unexposed infants.
Why the study?
Does maternal alcohol consumption and/or smoking during pregnancy alter autonomic nervous system function in full-term infants?
Observational
Does maternal alcohol consumption and/or smoking during pregnancy alter autonomic nervous system function in full-term infants?
Prenatal exposure to smoking and alcohol alters autonomic function in newborns, potentially providing early markers for SIDS risk.
May flag autonomic changes as early SIDS risk markers in exposed newborns; leaves open causality and requires prospective validation.
Prenatal exposure to smoking and alcohol increases the risk for Sudden Infant Death Syndrome (SIDS). Physiological changes associated with these exposures are not well studied. Full-term infants were tested within the first 3 days of life. We hypothesized that maternal alcohol consumption and/or smoking during pregnancy would alter autonomic nervous system function. Newborns whose mothers smoked during pregnancy had lower beat-to-beat heart rate variability in quiet sleep. Infants whose mothers consumed alcohol had lower global heart rate variability, but only in active sleep. Unexposed infants demonstrated increases in heart rate with head-up tilt and decreases in heart rate with head-down tilt, but smoking and alcohol-exposed infants showed no significant responses. These results indicate that autonomic function is altered by prenatal exposure to alcohol and smoking. Such markers may provide early identification of infants at greatest risk for SIDS.
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Fifer et al. (2009) conducted an observational in Prenatal exposure to smoking and alcohol. Prenatal exposure to smoking and alcohol vs. Unexposed infants was evaluated on Autonomic nervous system function (heart rate variability and heart rate response to tilt). Prenatal exposure to smoking and alcohol altered infant autonomic function, reducing heart rate variability and blunting heart rate responses to tilt compared to unexposed infants.
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