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Journal of Clinical Endocrinology & Metabolism, doi:10.1210/jc.2004-1388
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The Journal of Clinical Endocrinology & Metabolism Vol. 90, No. 2 695-699
Copyright © 2005 by The Endocrine Society

Cortisol Response to Ovine Corticotropin-Releasing Hormone in a Model of Pregnancy and Parturition in Euthymic Women with and without a History of Postpartum Depression

Miki Bloch, David R. Rubinow, Peter J. Schmidt, Angela Lotsikas, George P. Chrousos and Giovanni Cizza

Department of Psychiatry (M.B.), Tel-Aviv Sourasky Medical Center, Tel-Aviv, Israel 64239; Behavioral Endocrinology Branch (D.R.R., P.J.S.), National Institute of Mental Health, National Institutes of Health (NIH), Department of Health and Human Services, Bethesda, Maryland 20892-1276; and Pediatric and Reproductive Endocrinology Branch (A.L., G.P.C., G.C.), National Institute of Child Health and Human Development, NIH, U.S. Department of Health and Human Services, Bethesda, Maryland 20892-1853

Address all correspondence and requests for reprints to: David R. Rubinow, M.D., National Institute of Mental Health, Building 10, Room 3N238, 10 Center Drive, MSC 1276, Bethesda Maryland 20892-1276. E-mail: rubinowd{at}intra.nimh.nih.gov.

Hypothalamic-pituitary-adrenal axis abnormalities have been reported in depressed women and those with postpartum blues, compared with nondepressed women.

We investigated the effect of gonadal steroids on the hormonal response to ovine CRH in women with (n = 5) and without (n = 7) a past history of postpartum depression (PPD) by creating an endocrine model of pregnancy and the postpartum. Ovine CRH (1 µg/kg) stimulation tests were performed in the baseline follicular phase, during hormone addback (leuprolide acetate plus supraphysiologic doses of estradiol and progesterone-mimicking pregnancy), and after precipitous withdrawal of hormone replacement (mimicking the puerperium).

Significant phase by time (P < 0.005) and phase by diagnosis (P < 0.05) interactions were observed, reflecting increased stimulated cortisol during the supraphysiologic phase, particularly in subjects with a history of PPD. Cortisol area under the curve also showed a significant phase by diagnosis effect (P < 0.05). Significant increases during the supraphysiologic phase were also seen for urinary free cortisol (P < 0.05), cortisol area under the curve (P < 0.001), and plasma corticosteroid-binding globulin (P < 0.05).

Our data show that in humans, as in animals, supraphysiologic gonadal steroid levels enhance pituitary-adrenal axis activity, and, further, that women with a history of PPD have an enhanced sensitivity of the pituitary-adrenal axis to gonadal steroids.







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