Skip to main content
Archives of Disease in Childhood. Fetal and Neonatal Edition logoLink to Archives of Disease in Childhood. Fetal and Neonatal Edition
. 2005 Mar;90(2):F166–F169. doi: 10.1136/adc.2004.049320

Fetal plasma testosterone correlates positively with cortisol

R Gitau, D Adams, N Fisk, V Glover
PMCID: PMC1721847  PMID: 15724043

Abstract

Background: Fetal exposure to testosterone has been implicated in programming childhood behaviour, but little is known about the determinants of fetal testosterone concentrations.

Aims: To investigate the relation between fetal testosterone and maternal and fetal cortisol.

Methods: Clinically indicated blood samples taken from 44 human fetuses (mean gestational age 27 weeks, range 15–38), together with paired maternal samples, were analysed for testosterone and cortisol concentrations.

Results: Male fetuses had significantly higher concentrations of testosterone than females. Female but not male fetal concentrations rose significantly with gestational age. Fetal testosterone correlated positively with both fetal cortisol and maternal testosterone concentrations. Multiple regression showed that maternal testosterone and fetal cortisol were independently correlated with fetal plasma testosterone in both sexes.

Conclusion: Unlike the norm in the adult, where testosterone production is often inhibited by cortisol, in the fetus there is a positive link between the two.

Full Text

The Full Text of this article is available as a PDF (88.8 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Amitai D. B., Fichman S., Merlob P., Morad Y., Lapidoth M., Metzker A. Cutis marmorata telangiectatica congenita: clinical findings in 85 patients. Pediatr Dermatol. 2000 Mar-Apr;17(2):100–104. doi: 10.1046/j.1525-1470.2000.01723.x. [DOI] [PubMed] [Google Scholar]
  2. Beck-Peccoz P., Padmanabhan V., Baggiani A. M., Cortelazzi D., Buscaglia M., Medri G., Marconi A. M., Pardi G., Beitins I. Z. Maturation of hypothalamic-pituitary-gonadal function in normal human fetuses: circulating levels of gonadotropins, their common alpha-subunit and free testosterone, and discrepancy between immunological and biological activities of circulating follicle-stimulating hormone. J Clin Endocrinol Metab. 1991 Sep;73(3):525–532. doi: 10.1210/jcem-73-3-525. [DOI] [PubMed] [Google Scholar]
  3. Chatterton R. T., Jr, Dooley S. L. Reversal of diurnal cortisol rhythm and suppression of plasma testosterone in obstetric residents on call. J Soc Gynecol Investig. 1999 Jan-Feb;6(1):50–54. doi: 10.1177/107155769900600110. [DOI] [PubMed] [Google Scholar]
  4. Cumming D. C., Quigley M. E., Yen S. S. Acute suppression of circulating testosterone levels by cortisol in men. J Clin Endocrinol Metab. 1983 Sep;57(3):671–673. doi: 10.1210/jcem-57-3-671. [DOI] [PubMed] [Google Scholar]
  5. Finegan J. A., Bartleman B., Wong P. Y. A window for the study of prenatal sex hormone influences on postnatal development. J Genet Psychol. 1989 Mar;150(1):101–112. doi: 10.1080/00221325.1989.9914580. [DOI] [PubMed] [Google Scholar]
  6. Fujieda K., Faiman C., Reyes F. I., Winter J. S. The control of steroidogenesis by human fetal adrenal cells in tissue culture. I. Responses to adrenocorticotropin. J Clin Endocrinol Metab. 1981 Jul;53(1):34–38. doi: 10.1210/jcem-53-1-34. [DOI] [PubMed] [Google Scholar]
  7. Giannakoulopoulos X., Sepulveda W., Kourtis P., Glover V., Fisk N. M. Fetal plasma cortisol and beta-endorphin response to intrauterine needling. Lancet. 1994 Jul 9;344(8915):77–81. doi: 10.1016/s0140-6736(94)91279-3. [DOI] [PubMed] [Google Scholar]
  8. Giannakoulopoulos X., Teixeira J., Fisk N., Glover V. Human fetal and maternal noradrenaline responses to invasive procedures. Pediatr Res. 1999 Apr;45(4 Pt 1):494–499. doi: 10.1203/00006450-199904010-00007. [DOI] [PubMed] [Google Scholar]
  9. Gitau R., Cameron A., Fisk N. M., Glover V. Fetal exposure to maternal cortisol. Lancet. 1998 Aug 29;352(9129):707–708. doi: 10.1016/S0140-6736(05)60824-0. [DOI] [PubMed] [Google Scholar]
  10. Gitau R., Fisk N. M., Teixeira J. M., Cameron A., Glover V. Fetal hypothalamic-pituitary-adrenal stress responses to invasive procedures are independent of maternal responses. J Clin Endocrinol Metab. 2001 Jan;86(1):104–109. doi: 10.1210/jcem.86.1.7090. [DOI] [PubMed] [Google Scholar]
  11. Glover Vivette, O'Connor Thomas G., Heron Jonathan, Golding Jean, ALSPAC Study team Antenatal maternal anxiety is linked with atypical handedness in the child. Early Hum Dev. 2004 Sep;79(2):107–118. doi: 10.1016/j.earlhumdev.2004.04.012. [DOI] [PubMed] [Google Scholar]
  12. Grimshaw G. M., Sitarenios G., Finegan J. A. Mental rotation at 7 years: relations with prenatal testosterone levels and spatial play experiences. Brain Cogn. 1995 Oct;29(1):85–100. doi: 10.1006/brcg.1995.1269. [DOI] [PubMed] [Google Scholar]
  13. Karteris E., Randeva H. S., Grammatopoulos D. K., Jaffe R. B., Hillhouse E. W. Expression and coupling characteristics of the CRH and orexin type 2 receptors in human fetal adrenals. J Clin Endocrinol Metab. 2001 Sep;86(9):4512–4519. doi: 10.1210/jcem.86.9.7849. [DOI] [PubMed] [Google Scholar]
  14. Kinsley C. H., Bridges R. S. Prenatal stress and maternal behavior in intact virgin rats: response latencies are decreased in males and increased in females. Horm Behav. 1988 Mar;22(1):76–89. doi: 10.1016/0018-506x(88)90032-3. [DOI] [PubMed] [Google Scholar]
  15. Nass R., Baker S., Speiser P., Virdis R., Balsamo A., Cacciari E., Loche A., Dumic M., New M. Hormones and handedness: left-hand bias in female congenital adrenal hyperplasia patients. Neurology. 1987 Apr;37(4):711–715. doi: 10.1212/wnl.37.4.711. [DOI] [PubMed] [Google Scholar]
  16. O'Connor Thomas G., Heron Jonathan, Golding Jean, Beveridge Michael, Glover Vivette. Maternal antenatal anxiety and children's behavioural/emotional problems at 4 years. Report from the Avon Longitudinal Study of Parents and Children. Br J Psychiatry. 2002 Jun;180:502–508. doi: 10.1192/bjp.180.6.502. [DOI] [PubMed] [Google Scholar]
  17. O'Regan D., Welberg L. L., Holmes M. C., Seckl J. R. Glucocorticoid programming of pituitary-adrenal function: mechanisms and physiological consequences. Semin Neonatol. 2001 Aug;6(4):319–329. doi: 10.1053/siny.2001.0067. [DOI] [PubMed] [Google Scholar]
  18. Obel Carsten, Hedegaard Morten, Henriksen Tine Brink, Secher Niels Jørgen, Olsen Jørn. Psychological factors in pregnancy and mixed-handedness in the offspring. Dev Med Child Neurol. 2003 Aug;45(8):557–561. doi: 10.1017/s0012162203001014. [DOI] [PubMed] [Google Scholar]
  19. Rodeck C. H., Gill D., Rosenberg D. A., Collins W. P. Testosterone levels in midtrimester maternal and fetal plasma and amniotic fluid. Prenat Diagn. 1985 May-Jun;5(3):175–181. doi: 10.1002/pd.1970050303. [DOI] [PubMed] [Google Scholar]
  20. Smith R., Mesiano S., Chan E. C., Brown S., Jaffe R. B. Corticotropin-releasing hormone directly and preferentially stimulates dehydroepiandrosterone sulfate secretion by human fetal adrenal cortical cells. J Clin Endocrinol Metab. 1998 Aug;83(8):2916–2920. doi: 10.1210/jcem.83.8.5020. [DOI] [PubMed] [Google Scholar]
  21. Vandenbergh J. G., Huggett C. L. The anogenital distance index, a predictor of the intrauterine position effects on reproduction in female house mice. Lab Anim Sci. 1995 Oct;45(5):567–573. [PubMed] [Google Scholar]
  22. Ward I. L. The prenatal stress syndrome: current status. Psychoneuroendocrinology. 1984;9(1):3–11. doi: 10.1016/0306-4530(84)90016-7. [DOI] [PubMed] [Google Scholar]
  23. Weinstock M. Alterations induced by gestational stress in brain morphology and behaviour of the offspring. Prog Neurobiol. 2001 Dec;65(5):427–451. doi: 10.1016/s0301-0082(01)00018-1. [DOI] [PubMed] [Google Scholar]

Articles from Archives of Disease in Childhood. Fetal and Neonatal Edition are provided here courtesy of BMJ Publishing Group

RESOURCES