Journal
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY
Volume 297, Issue 2, Pages R510-R514Publisher
AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpregu.00175.2009
Keywords
placenta; fetal sex
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Funding
- John Hunter Children's Research Foundation
- Emelyn and Jennie Thomas Cardiovascular Research Scholarship
- University of Newcastle External Scholarship
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Stark MJ, Wright IMR, Clifton VL. Sex-specific alterations in placental 11 beta-hydroxysteroid dehydrogenase 2 activity and early postnatal clinical course following antenatal betamethasone. Am J Physiol Regul Integr Comp Physiol 297: R510-R514, 2009. First published June 17, 2009; doi:10.1152/ajpregu.00175.2009.-Placental 11 beta-hydroxysteroid dehydrogenase-2 (11 beta HSD2) limits fetal glucocorticoid exposure and is associated with physiological stability in the premature newborn infant. Antenatal betamethasone alters 11 beta HSD2 activity and confers sex-specific advantages in neonatal outcome. We investigated the influence of betamethasone and sex on 11 beta HSD2 activity, neonatal adrenal function and clinical course in 24-to 36-wk gestation neonates from birth to day 5 of life. Univariate analyses demonstrated an interaction between timing of betamethasone exposure and sex for 11 beta HSD2 activity rate (P = 0.02) and umbilical arterial cortisol (P = 0.01). For infants born < 72 h following antenatal betamethasone, females had higher 11 beta HSD2 activity (P < 0.01) and umbilical arterial cortisol (P = 0.01) than males. Females born < 72 h of betamethasone exposure had higher day 1 urinary cortisol, if exposed to perinatal stress, than males (P < 0.01). For infants born < 72 h after betamethasone exposure, 11 beta HSD2 activity was negatively correlated with Clinical Illness Severity Score score (r = -0.79 P = 0.01) and positively correlated with mean arterial blood pressure (r = 0.8 P = 0.01) only in females. Sex-specific placental 11BHSD2 autoregulation following antenatal betamethasone exposure may limit adrenal suppression in females influencing physiological stability following preterm birth. A lack of adjustment in 11 beta HSD2 and adrenal response may contribute to the increased incidence of poor outcome observed in preterm males.
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