Literature DB >> 233672

Pituitary-adrenal axis activity in treated congenital adrenal hyperplasia: static and dynamic studies.

M T Pham-Huu-Trung, M Gourmelen, M C Raux-Eurin, F Girard.   

Abstract

The pituitary-adrenal axis activity was evaluated in 43 patients, treated for congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency, by measuring plasma ACTH, 17-hydroxyprogesterone (17-OHP), testosterone, and aldosterone. Dynamic studies were performed by injecting 250 micrograms synthetic ACTH im and collecting blood samples 1 h later for steroid analysis. Twelve to fourteen hours after the last hydrocortisone dose given the evening before, plasma ACTH fluctuated widely from less than 10-475 pg/ml, 17-OHP exceeded normal values and varied from 1-275 ng/ml, while testosterone ranged from 3-151 ng/100 ml. The correlations between ACTH and 17-OHP (n equal 61, r equal 0.665, P less than 0.001) and between 17-OHP and testosterone (n = 43, r = 0.761, P less than 0.001) were good, while that between 17-OHP and aldosterone (n = 64, r = 0.512, P less than 0.001) was rather poor. One hour after ACTH injection, the mean level of 17-OHP was significantly increased as compared to the mean basal level [96.8 ng/ml +/- 10.6 (SE) as compared to 67.0 ng/ml +/- 8.1 (SE)]. However, only 12 out of the 48 tests showed a positive response equal to or greater than 100%, and the majority of these responses (10 out of 12) occurred when basal levels of 17-OHP were between 10-70 ng/ml. This suggests that when basal levels fall outside these values, the pituitary-adrenal axis is either too inhibited or too stimulated to react to exogenous ACTH. Of the 48 tests where 17-OHP was measured, 23 had basal level values within these limits, the mean being 40.3 ng/ml. The corresponding mean ACTH level was 99 pg/ml with a wide range (1-230 pg/ml). On the other hand, in prepubertal children who exhibited 17-OHP concentrations between 10-70 ng/ml, testosterone varied from 3-30 ng/100 ml, with a mean of 16.0 ng/100 ml +/- 1.9 (SE) which is not different from the mean level found in normal children [14.0 ng/100 ml +/- 1.3 (SE)]. Thus, under the influence of endogenous ACTH which is moderately increased, 17-OHP concentrations far exceed normal values, whereas plasma testosterone seems to be unaffected.

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Year:  1978        PMID: 233672     DOI: 10.1210/jcem-47-2-422

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  5 in total

Review 1.  Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a review of current knowledge.

Authors:  G E Bacon; R P Kelch
Journal:  J Endocrinol Invest       Date:  1979 Jan-Mar       Impact factor: 4.256

2.  Lack of prolactin involvement in corticosteroid secretion.

Authors:  J N Hugues; E Modigliani; F Girard; J Sebaoun
Journal:  J Endocrinol Invest       Date:  1987-02       Impact factor: 4.256

3.  Selective venous catheterization in the evaluation of hyperandrogenism.

Authors:  C Bricaire; A Raynaud; A Benotmane; F Clair; B Paniel; I Mowszowicz; F Wright; J F Moreau; F Kuttenn; P Mauvais-Jarvis
Journal:  J Endocrinol Invest       Date:  1991-12       Impact factor: 4.256

4.  [Silent adrenal gland tumors in patients with adrenogenital syndrome].

Authors:  S Jaresch; R Schlaghecke; R Jungblut; H L Krüskemper; H K Kley
Journal:  Klin Wochenschr       Date:  1987-07-15

5.  Congenital adrenal hyperplasia in a 66-year-old female.

Authors:  A D Wright; T C Harvey; G Holder; D C Anderson; B T Rudd
Journal:  Postgrad Med J       Date:  1981-05       Impact factor: 2.401

  5 in total

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