19-Nor-Deoxycorticosterone Excretion in Primary Aldosteronism and Low Renin Hypertension*
- 1 February 1983
- journal article
- research article
- Published by The Endocrine Society in Journal of Clinical Endocrinology & Metabolism
- Vol. 56 (2) , 218-221
- https://doi.org/10.1210/jcem-56-2-218
Abstract
Nonaldosterone mineralocorticoids, such as deoxycorticosterone (DOC) and 18-hydroxy-DOC, have been reported to be elevated in some patients with primary aldosteronism (PA). Since DOC is a probable precursor of a more potent mineralocorticoid, 19-nor-deoxycorticosterone (19-nor-DOC), this study evaluated urinary free (UF) 19-nor-DOC excretion in 6 patients with PA and compared the results to those from 11 patients with low renin hypertension (LRH) and 7 normotensive subjects. PA was due to either an aldosteroneproducing adenoma (APA; 4 patients) or bilateral adrenal hyperplasia (2 patients) diagnosed by adrenal venous catheterization or surgery. Compared to LRH subjects, patients with PA had a higher mean blood pressure (137 ±9 vs. 114 ± 3 mm Hg), a lower plasma potassium level (3.1 ± 0.2 vs. 3.9 ±0.1 meq/1) and greater renin suppression (0.3 ±0.1 vs. 0.6 ± 0.1 ng angiotensin I/ml-h). UF 19-nor-DOC levels were elevated in PA subjects compared to those in normotensives (3,716 ± 1,517 vs. 428 ±112 ng/day) but not compared to those in LRH patients (1,237 ± 471). Two patients with APA had distinctly elevated UF 19-nor-DOC levels (11,137 and 7,744 ng/day), but another APA patient had the lowest value (305 ng/day). UF 19-nor-DOC positively correlated with the aldosterone secretion rate in PA (r = 0.75) but not LRH subjects. In conclusion, this study demonstrates that patients with PA may have elevated levels of UF 19-nor-DOC which are proportional to the aldosterone excess and could be a contributing factor to the hypertension, hypokalamia, and excess mineralocorticoid activity of this disease.Keywords
This publication has 9 references indexed in Scilit:
- Identification of 19-Hydroxydeoxycorticosterone, 19-Oxo-Deoxycorticosterone, and 19-Oic-Deoxycorticosterone as Products of Deoxycorticosterone Metabolism by Rat Adrenals*Endocrinology, 1982
- 19-Nor-deoxycorticosterone in the neutral fraction of human urineSteroids, 1981
- 19-Nor Analogs of Adrenal Steroids: Mineralocorticoid and Glucocorticoid Receptor Activity*Endocrinology, 1980
- Low Renin Essential Hypertension: Failure to Demonstrate Excess 11-Deoxycorticosterone Production*Journal of Clinical Endocrinology & Metabolism, 1979
- 19-Nor-Deoxycorticosterone: A Potent Mineralcocorticoid Isolated from the Urine of Rats with Regenerating Adrenals*Endocrinology, 1979
- 19-NOR DEOXYCORTKOSTERONE (19-nor DOC): MINERALOCORTICOID RECEPTOR AFFINITY HIGHER THAN ALDOSTERONE, ELECTROLYTE ACTIVITY LOWER.+Endocrinology, 1978
- Urinary Free 18-Hydroxy-ll-Desoxycorticosterone Excretion in Normal and Hypertensive Patients*Journal of Clinical Endocrinology & Metabolism, 1978
- The measurement of urinary tetrahydroaldosterone by radioimmunoassayThe Journal of Steroid Biochemistry and Molecular Biology, 1977
- Sodium Retaining Activity of 19-Nor-Steroids in Adrenalectomized RatsExperimental Biology and Medicine, 1957