Author:
Pham-Huu-Trung M. T.,Raux M. C.,Gourmelen M.,Baron M. C.,Girard F.,Marrec D.
Abstract
ABSTRACT
Plasma aldosterone and 17α-hydroxyprogesterone (17-OHP) concentrations were measured in 35 patients with congenital adrenal hyperplasia resulting from 21-hydroxylase deficiency. Ten patients had never been treated and among them were 4 salt-losing infants. Both aldosterone and 17-OHP were high in the 6 untreated non salt-losers. The values ranged respectively from 110 to 376 pg/ml and from 150 to 292 ng/ml. Results were variable in the 4 salt-losers. Three out of 5 untreated non salt-losers who were submitted to a low sodium diet, responded by doubling their aldosterone levels.
When plasma 17-OHP concentrations were < 30 ng/ml, the mean aldosterone level in the treated non salt-losers (n = 6) was 15.3 pg/ml ± 4.3 (se). This value was not different from the mean level found in the control children (n = 7), 18.8 pg/ml ± 3.2. In the treated salt-losers (n = 9), the measured aldosterone levels were ≦ 10 pg/ml 7 times out of 9. When the treated patients exhibited plasma 17-OHP concentrations > 30 ng/ml, the salt-losers (n = 11) were distinguished from the non salt-losers (n = 8) in that they showed a significantly lower aldosterone mean level, 24.6 pg/ml ± 4.3 against 69 pg/ml ± 13.4 found in the non salt-losers.
The salt-losers displayed no aldosterone increases to synthetic ACTH stimulation under treatment or at the withdrawal of treatment, while positive aldosterone responses were often observed in the non salt-losers. In the latter group, studied under different conditions (with and without therapy, on low sodium diet, after ACTH test) a significant correlation was found between aldosterone and 17-OHP levels expressed in log. values, (n = 38, r = 0.80, P < 0.001). The relationship could also be established with the values obtained from all the salt-losers, but it was less significant, (n = 35, r = 0.46, P < 0.02).
Subject
Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism
Cited by
14 articles.
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