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 5alpha/beta-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.

Department of Gynecology and Obstetrics General University Hospital and 1st Faculty ofMedicine Charles University Prague Czech Republic

Department of Pediatrics and Adolescent Medicine General UniversityHospital and 1st Faculty of Medicine of Charles University Prague Czech Republic

Institute of Endocrinology Prague Czech Republic

Institute of Endocrinology Prague CzechRepublic

Institute of Medical Biochemistry and Laboratory Diagnostics and 4th Department ofInternal Medicine General University Hospital and 1st Faculty of Medicine of Charles Universityin Prague Czech Republic

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