Tolvaptan-induced isolated elevation of bilirubin in a patient with Gilbert syndrome

SAGE Open Med Case Rep. 2023 Apr 29:11:2050313X231169841. doi: 10.1177/2050313X231169841. eCollection 2023.

Abstract

Tolvaptan is the current standard of treatment for autosomal dominant polycystic kidney disease. It operates by acting on V2 receptors and blocks vasopressin interactions, causing a reduction in the rate of renal cyst growth and preserving kidney function. The current known risks of tolvaptan involve a serious liver injury characterized by an elevation in total bilirubin and alanine transaminase and aspartate transaminase levels. In this report, we document a unique liver injury characterized by an elevated bilirubin with normal alanine transaminase and aspartate transaminase levels in a patient who is homozygous for the UGT1A1 consistent with Gilbert syndrome.

Keywords: Gilbert’s syndrome; Tolvaptan; autosomal dominant polycystic kidney disease.

Publication types

  • Case Reports