ACTH stimulation tests and plasma dehydroepiandrosterone sulfate levels in women with hirsutism - PubMed (original) (raw)
. 1990 Sep 27;323(13):849-54.
doi: 10.1056/NEJM199009273231301.
Affiliations
- PMID: 2168515
- DOI: 10.1056/NEJM199009273231301
Free article
ACTH stimulation tests and plasma dehydroepiandrosterone sulfate levels in women with hirsutism
S F Siegel et al. N Engl J Med. 1990.
Free article
Abstract
Background: Hirsutism in women is a clinical manifestation of excessive production of androgens. The source of the excess androgen may be either the ovaries or the adrenal glands, and distinguishing between these sources may be difficult.
Methods: To determine whether measurements of plasma dehydroepiandrosterone (DHEA) sulfate and ACTH stimulation tests, both widely used in the evaluation of hirsutism in women, provide useful information, we performed both tests in 22 normal women and 31 female patients with hirsutism. The hormones measured in plasma during the ACTH stimulation tests were progesterone, 17-hydroxypregnenolone, 17-hydroxyprogesterone, DHEA, androstenedione, 11-deoxycortisol, and cortisol.
Results: The women with hirsutism were divided into four groups based on their individual responses to ACTH stimulation: patients with a possible 3 beta-hydroxy-delta 5-steroid dehydrogenase deficiency, those with a possible 21-hydroxylase deficiency, those with a possible 11 beta-hydroxylase deficiency, and those with no apparent defect in steroidogenesis. The results in 19 patients (61 percent) suggested subtle defects in adrenal steroidogenesis. There was no significant correlation between the basal plasma DHEA sulfate levels and the hormonal response to ACTH, nor were the basal levels of hormones predictive of the levels after ACTH stimulation. Eleven patients had significantly elevated basal levels of plasma DHEA sulfate; only 5 of these 11 had responses to ACTH suggestive of compromised steroidogenesis. Thirteen patients who had responses suggestive of defective steroidogenesis had DHEA sulfate levels within the normal range.
Conclusions: A substantial proportion of women with hirsutism have mild defects in adrenal steroidogenesis, revealed by an ACTH stimulation test, that are indicative of late-onset (nonclassic) congenital adrenal hyperplasia. Measurements of basal steroid levels are not helpful in differentiating among the causes of increased androgen production in such patients and may be misleading.
Comment in
- ACTH stimulation tests in women with hirsutism.
Dewailly D. Dewailly D. N Engl J Med. 1991 Feb 21;324(8):564-5. doi: 10.1056/NEJM199102213240814. N Engl J Med. 1991. PMID: 1846941 No abstract available. - Hirsutism--beyond the steroidogenic block.
Ehrmann DA, Rosenfield RL. Ehrmann DA, et al. N Engl J Med. 1990 Sep 27;323(13):909-11. doi: 10.1056/NEJM199009273231309. N Engl J Med. 1990. PMID: 2168517 No abstract available.
Similar articles
- [Defects of adrenal steroidogenesis in patients with hirsutism].
Salinas Vert I, Audí Parera L, Granada Ybern ML, Lucas Martín A, Pizarro Lozano E, Foz Sala M, Sanmartí Sala A. Salinas Vert I, et al. Med Clin (Barc). 1998 Feb 14;110(5):171-6. Med Clin (Barc). 1998. PMID: 9547720 Spanish. - Adrenal androgen hyperresponsiveness to adrenocorticotropin in women with acne and/or hirsutism: adrenal enzyme defects and exaggerated adrenarche.
Lucky AW, Rosenfield RL, McGuire J, Rudy S, Helke J. Lucky AW, et al. J Clin Endocrinol Metab. 1986 May;62(5):840-8. doi: 10.1210/jcem-62-5-840. J Clin Endocrinol Metab. 1986. PMID: 3007557 - The value of low dose (1 microg) ACTH stimulation test in the investigation of non-classic adrenal hyperplasia due to 11beta-hydroxylase deficiency.
Unlühizarci K, Keleştimur F, Güven M, Bayram F, Colak R. Unlühizarci K, et al. Exp Clin Endocrinol Diabetes. 2002 Nov;110(8):381-5. doi: 10.1055/s-2002-36422. Exp Clin Endocrinol Diabetes. 2002. PMID: 12518247 Clinical Trial. - The adrenal cortex and virilization.
McKenna TJ, Cunningham SK, Loughlin T. McKenna TJ, et al. Clin Endocrinol Metab. 1985 Nov;14(4):997-1020. doi: 10.1016/s0300-595x(85)80086-4. Clin Endocrinol Metab. 1985. PMID: 3002682 Review. - [Congenital adrenal hyperplasia].
Stanić M, Nesović M. Stanić M, et al. Med Pregl. 1999 Nov-Dec;52(11-12):447-54. Med Pregl. 1999. PMID: 10748766 Review. Croatian.
Cited by
- The next 150 years of congenital adrenal hyperplasia.
Turcu AF, Auchus RJ. Turcu AF, et al. J Steroid Biochem Mol Biol. 2015 Sep;153:63-71. doi: 10.1016/j.jsbmb.2015.05.013. Epub 2015 Jun 3. J Steroid Biochem Mol Biol. 2015. PMID: 26047556 Free PMC article. Review. - Adrenocortical steroid response to ACTH in different phenotypes of non-obese polycystic ovary syndrome.
Cinar N, Harmanci A, Aksoy DY, Aydin K, Yildiz BO. Cinar N, et al. J Ovarian Res. 2012 Dec 7;5(1):42. doi: 10.1186/1757-2215-5-42. J Ovarian Res. 2012. PMID: 23216997 Free PMC article. - Value of buserelin testing in the evaluation of hirsute women.
Ambrosi B, Re T, Passini E, Bochicchio D, Ferrario R. Ambrosi B, et al. J Endocrinol Invest. 1996 Apr;19(4):204-9. doi: 10.1007/BF03349868. J Endocrinol Invest. 1996. PMID: 8862498 - ACP Broadsheet 131: March 1992. Hirsute women: should they be investigated?
Barth JH. Barth JH. J Clin Pathol. 1992 Mar;45(3):188-92. doi: 10.1136/jcp.45.3.188. J Clin Pathol. 1992. PMID: 1556225 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources