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Normoreninemic hypoaldosteronism in a case of isolated ACTH deficiency.

Abstract
This paper documents the rare and hitherto unreported association between isolated ACTH deficiency and normoreninemic hypoaldosteronism in a 63-year-old woman. Baseline plasma aldosterone and 18-hydroxycorticosterone were extremely low. Both steroids did not respond to exogenous angiotensin II infusion, whereas they were increased in parallel to ACTH stimulation. Thus, acquired dysfunction or congenital dysgenesis of the zona glomerulosa was suspected. The upright posture-furosemide test showed a subnormal but definite plasma aldosterone response coupled with a normal increase in plasma renin activity, indicating that there may be a yet unidentified mechanism(s) underlying the postural increase of aldosterone.
AuthorsS Miyabo, M Minami, T Inazu, T Tamai, N Aoyagi, K Miyanaga, E Ooya, S Kishida, T Nakai
JournalHormone research (Horm Res) Vol. 31 Issue 4 Pg. 163-8 ( 1989) ISSN: 0301-0163 [Print] Switzerland
PMID2551810 (Publication Type: Case Reports, Journal Article)
Chemical References
  • 17-Hydroxycorticosteroids
  • Pituitary Hormones, Anterior
  • Angiotensin II
  • Aldosterone
  • 18-Hydroxycorticosterone
  • Adrenocorticotropic Hormone
  • Renin
Topics
  • 17-Hydroxycorticosteroids (urine)
  • 18-Hydroxycorticosterone (blood)
  • Adrenocorticotropic Hormone (analysis, deficiency)
  • Aldosterone (blood)
  • Angiotensin II (blood, pharmacology)
  • Blood Pressure (drug effects)
  • Female
  • Humans
  • Hypoaldosteronism (complications)
  • Infusions, Intravenous
  • Middle Aged
  • Pituitary Hormones, Anterior (blood)
  • Radioimmunoassay
  • Renin (blood)

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