Journal article
Authors list: Lamade, Eva Kathrin; Hendlmeier, Ferdinand; Wudy, Stefan A.; Witt, Stephanie H.; Rietschel, Marcella; Coenen, Michaela; Gilles, Maria; Deuschle, Michael
Publication year: 2021
Pages: 1630-1636
Journal: The Journal of Clinical Endocrinology & Metabolism
Volume number: 106
Issue number: 6
ISSN: 0021-972X
eISSN: 1945-7197
Open access status: Bronze
DOI Link: https://doi.org/10.1210/clinem/dgab113
Publisher: Oxford University Press
Context: Excess glucocorticoids impact fetal health. Maternal glucocorticoids peak in early morning. Fetoplacental 11 beta-hydroxysteroid dehydrogenase type 2 (11 beta-HSD2) inactivates cortisol to cortisone, protecting the fetus from high glucocorticoids. However, time-specific alterations of human fetoplacental 11 beta-HSD2 have not been studied. Objective: We hypothesized that fetoplacental 11 beta-HSD2 activity shows time-specific alteration and acute affective or anxiety disorders impact fetoplacental 11 beta-HSD2 activity. Methods: In this observational study we investigated 78 pregnant European women undergoing amniocentesis (15.9 +/- 0.9 weeks of gestation). Amniotic fluid was collected (8:00 to 16:30 hours) for analysis of fetoplacental 11 beta-HSD2 activity, using cortisol (F):cortisone (E) ratio in amniotic fluid, E/(E + F). Fetoplacental 11 beta-HSD2 rhythm and association with "acute affective or anxiety disorder" (patients with at least one of: a major depressive episode, specific phobia, panic disorder, generalized anxiety disorder, mixed anxiety and depressive disorder) and "acute anxiety disorder" (one of: panic disorder, generalized anxiety disorder, mixed anxiety, depressive disorder), assessed using Mini International Neuropsychiatric Interview, were investigated. Results: Activity of 11 beta-HSD2 correlated with time of amniocentesis, peaking in the morning (r = -0.398; P < 0.001) and increased with acute affective or anxiety disorder (mean [M] = 0.70 vs M = 0.74; P = 0.037) and acute anxiety disorder (M = 0.70 vs M = 0.75; P = 0.016). These associations remained significant when controlling for confounders. 11 beta-HSD2 activity correlated negatively with pre-pregnancy body mass index (r = -0.225; P = 0.047). Conclusion: Our study indicates a time-specific alteration of fetoplacental 11 beta-HSD2 activity with peaking levels in the morning, demonstrating a mechanism of fetal protection from the morning maternal glucocorticoid surge.
Abstract:
Citation Styles
Harvard Citation style: Lamade, E., Hendlmeier, F., Wudy, S., Witt, S., Rietschel, M., Coenen, M., et al. (2021) Rhythm of Fetoplacental 11β-Hydroxysteroid Dehydrogenase Type 2-Fetal Protection From Morning Maternal Glucocorticoids, The Journal of Clinical Endocrinology & Metabolism, 106(6), pp. 1630-1636. https://doi.org/10.1210/clinem/dgab113
APA Citation style: Lamade, E., Hendlmeier, F., Wudy, S., Witt, S., Rietschel, M., Coenen, M., Gilles, M., & Deuschle, M. (2021). Rhythm of Fetoplacental 11β-Hydroxysteroid Dehydrogenase Type 2-Fetal Protection From Morning Maternal Glucocorticoids. The Journal of Clinical Endocrinology & Metabolism. 106(6), 1630-1636. https://doi.org/10.1210/clinem/dgab113
Keywords
11 beta-hydroxysteroid dehydrogenase; AMNIOTIC-FLUID GLUCOCORTICOIDS; circadian; CLOCK GENES; CORTISOL STRESS REACTIVITY; FETAL; fetoplacental; PLACENTAL 11-BETA-HSD2