In Vivo 11β-Hydroxysteroid Dehydrogenase Inhibition in Posaconazole-Induced Hypertension and Hypokalemia

Antimicrob Agents Chemother. 2017 Jul 25;61(8):e00760-17. doi: 10.1128/AAC.00760-17. Print 2017 Aug.

Abstract

We describe a case of apparent mineralocorticoid excess (AME) secondary to posaconazole therapy and suggest the biochemical mechanism. Clinical and laboratory investigation confirmed 11β-hydroxysteroid dehydrogenase inhibition and withholding therapy led to a resolution of all clinical and laboratory abnormalities. Posaconazole was later restarted at a lower dose and prevented recurrence of this syndrome. Additional studies are necessary to determine the frequency of posaconazole-induced AME and whether other azole antifungals can be associated with this phenomenon.

Keywords: antifungal; posaconazole; side effects.

Publication types

  • Case Reports

MeSH terms

  • 11-beta-Hydroxysteroid Dehydrogenases / antagonists & inhibitors*
  • Aged
  • Antifungal Agents / adverse effects*
  • Antifungal Agents / therapeutic use
  • Cortisone / blood
  • Humans
  • Hydrocortisone / blood
  • Hypertension / chemically induced*
  • Hypokalemia / chemically induced*
  • Lung / microbiology
  • Lung / pathology
  • Male
  • Mineralocorticoid Excess Syndrome, Apparent / chemically induced*
  • Pulmonary Aspergillosis / drug therapy
  • Triazoles / adverse effects*
  • Triazoles / therapeutic use

Substances

  • Antifungal Agents
  • Triazoles
  • posaconazole
  • 11-beta-Hydroxysteroid Dehydrogenases
  • Cortisone
  • Hydrocortisone