May Circulating Steroids Reveal a Predisposition to Intrahepatic Cholestasis of Pregnancy in Non-Pregnant Women?
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Published:2018-11-12
Issue:
Volume:
Page:S499-S510
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ISSN:1802-9973
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Container-title:Physiological Research
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language:en
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Short-container-title:Physiol Res
Author:
ŠIMJÁK P.,HILL M.,PAŘÍZEK A.,VÍTEK L.,VELÍKOVÁ M.,DUŠKOVÁ M.,KANCHEVA R.,BULANT J.,KOUCKÝ M.,KOKRDOVÁ Z.,ADAMCOVÁ K.,ČERNÝ A.,HÁJEK Z.,STÁRKA L.
Abstract
Intrahepatic cholestasis of pregnancy (ICP) is a frequent liver disorder, mostly occurring in the third trimester. ICP is not harmful to the mothers but threatens the fetus. The authors evaluated steroid alterations in maternal and mixed umbilical blood to elucidate their role in the ICP development. Ten women with ICP were included in the study. Steroids in the maternal blood were measured by Gas Chromatography-Mass Spectrometry (GC-MS) (n=58) and RIA (n=5) at the diagnosis of ICP, labor, day 5 postpartum, week 3 postpartum and week 6 postpartum. The results were evaluated by ANOVA consisting of the subject factor, between subject factors ICP, gestational age at the diagnosis of ICP and gestational age at labor, within-subject factor Stage and ICP × Stage interaction. The 17 controls were firstly examined in the week 36 of gestation. ICP patients showed reduced CYP17A1 activity in the C17,20 lyase step thus shifting the balance between the toxic conjugated pregnanediols and harmless sulfated 5α/β-reduced-17-oxo C19 steroids. Hence, more toxic metabolites originating in maternal liver from the placental pregnanes may penetrate backward to the fetal circulation. As these alterations persist in puerperium, the circulating steroids could be potentially used for predicting the predisposition to ICP even before next pregnancy.
Publisher
Institute of Physiology of the Czech Academy of Sciences
Subject
General Medicine,Physiology
Reference39 articles.
1. ABU-HAYYEH S, PAPACLEOVOULOU G, LOVGREN-SANDBLOM A, TAHIR M, ODUWOLE O, JAMALUDIN NA, RAVAT S, NIKOLOVA V, CHAMBERS J, SELDEN C, REES M, MARSCHALL HU, PARKER MG, WILLIAMSON C: Intrahepatic cholestasis of pregnancy levels of sulfated progesterone metabolites inhibit farnesoid X receptor resulting in a cholestatic phenotype. Hepatology 57: 716-726, 2013. 2. ABU-HAYYEH S, OVADIA C, LIEU T, JENSEN DD, CHAMBERS J, DIXON PH, LOVGREN-SANDBLOM A, BOLIER R, TOLENAARS D, KREMER AE, SYNGELAKI A, NOORI M, WILLIAMS D, MARIN JJ, MONTE MJ, NICOLAIDES KH, BEUERS U, OUDE-ELFERINK R, SEED PT, CHAPPELL L, MARSCHALL HU, BUNNETT NW, WILLIAMSON C: Prognostic and mechanistic potential of progesterone sulfates in intrahepatic cholestasis of pregnancy and pruritus gravidarum. Hepatology 63: 1287-1298, 2016. 3. ANAKK S, WATANABE M, OCHSNER SA, MCKENNA NJ, FINEGOLD MJ, MOORE DD: Combined deletion of Fxr and Shp in mice induces Cyp17a1 and results in juvenile onset cholestasis. J Clin Invest 121: 86-95, 2011. 4. BIASON-LAUBER A, MILLER WL, PANDEY AV, FLUCK CE: Of marsupials and men: "Backdoor" dihydrotestosterone synthesis in male sexual differentiation. Mol Cell Endocrinol 371: 124-132, 2013. 5. BYRNE JA, STRAUTNIEKS SS, MIELI-VERGANI G, HIGGINS CF, LINTON KJ, THOMPSON RJ: The human bile salt export pump: characterization of substrate specificity and identification of inhibitors. Gastroenterology 123: 1649-1658, 2002.
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