Primary aldosteronism treated by trilostane (3,β-hydroxysteroid dehydrogenase inhibitor)

The practicability and tolerability of trilostane, a competitive inhibitor of 3β-hydroxysteroid-Δ 5-dehydrogenase, for the therapy of primary aldosteronism was assessed in 1 patient with aldosterone-producing adenoma (APA) and 3 subjects with idiopathic adrenal hyperplasia (IHA). Trilostane afforded...

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Published inUrology (Ridgewood, N.J.) Vol. 25; no. 2; pp. 207 - 214
Main Authors Nakada, Teruhiro, Kazama, Taizo, Koike, Hiroshi, Yoshikawa, Munehide, Ishikawa, Shigeaki, Katayama, Takashi
Format Journal Article
LanguageEnglish
Published New York, NY Elsevier Inc 01.02.1985
Elsevier Science
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Summary:The practicability and tolerability of trilostane, a competitive inhibitor of 3β-hydroxysteroid-Δ 5-dehydrogenase, for the therapy of primary aldosteronism was assessed in 1 patient with aldosterone-producing adenoma (APA) and 3 subjects with idiopathic adrenal hyperplasia (IHA). Trilostane afforded reduction of plasma levels of aldosterone, progesterone, deoxycorticosterone, 17-OH progesterone, cortisol, Δ 4- androstenedione, and urinary excretion of 17-hydroxycorticosteroid. Conversely, circulating levels of dehydroepiandrosterone, dehydroepiandrosterone sulfate, and urinary excretion of 17-ketosteroids were increased following this drug therapy. Suppression of mineralo- or glucocorticoid biosynthesis was accompanied by an increase in plasma renin activity. One patient with APA or 3 subjects with IHA showed slight or remarkable improvement of hypertension and hypokalemia. Based on these findings, efficacy and tolerability of trilostane appear to aid in the treatment of IHA.
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ISSN:0090-4295
1527-9995
DOI:10.1016/0090-4295(85)90548-5