CORTICOTROPIN-RELEASING HORMONE AND CORTICOTROPIN-RELEASING HORMONE-BINDING PROTEIN IN NORMAL AND PREECLAMPTIC HUMAN PREGNANCIES

Citation
Av. Perkins et al., CORTICOTROPIN-RELEASING HORMONE AND CORTICOTROPIN-RELEASING HORMONE-BINDING PROTEIN IN NORMAL AND PREECLAMPTIC HUMAN PREGNANCIES, British journal of obstetrics and gynaecology, 102(2), 1995, pp. 118-122
Citations number
21
Categorie Soggetti
Obsetric & Gynecology
ISSN journal
03065456
Volume
102
Issue
2
Year of publication
1995
Pages
118 - 122
Database
ISI
SICI code
0306-5456(1995)102:2<118:CHACH>2.0.ZU;2-A
Abstract
Objective To measure the plasma levels of corticotrophin-releasing hor mone and corticotrophin-releasing hormone binding protein in normal pr egnancy and in pregnancies complicated by pre-eclampsia. Setting John Radcliffe Hospital, Oxford and St Thomas's Hospital, London. Subjects One hundred and twenty pregnant women sampled prospectively throughout gestation, of whom 91 experienced a normal pregnancy and eight develo ped pre-eclampsia; in a second study, 10 women with severe pre-eclamps ia, presenting at a range of gestational ages, were sampled once and c ompared with appropriately matched normal pregnant women. Main outcome measure Plasma levels of corticotrophin-releasing hormone determined by immunoradiometric assay. Plasma levels of corticotrophin-releasing hormone binding protein measured by direct radioimmunoassay. Results I n the prospective study, plasma samples from women with pre-eclampsia exhibited higher (390.2 versus 292.7 pmol/l at 36 weeks) levels of cor ticotrophin-releasing hormone and significantly lower (5.24 versus 8.1 4 nmol/l at 36 weeks, P < 0.002) levels of corticotrophin-releasing ho rmone binding protein than normal controls. In the second, single time point study a significant elevation in CRH (P < 0.002) and reduction in CRH-BP (P < 0.001) was found in pre-eclamptic pregnancies compared with controls. Conclusions In human pregnancies complicated by pre-ecl ampsia there is an elevated level of corticotrophin releasing hormone whilst there is less corticotrophin-releasing hormone binding protein; therefore there is a net increase in free potentially bioactive hormo ne which may play a role in the pathology of the disease.