Related Experiment Video
Updated: Jan 8, 2026

Establishment and Validation of a Rat Model of Pulmonary Arterial Hypertension Associated with Pulmonary Fibrosis
Published on: May 23, 2025
Malignant hypertension and pseudohyperaldosteronism associated with rifampicin therapy
Alexandre Szedleski1,2, Cédric Ilbert3, Véronique Goncette4
1Division of Nephrology, University of Liège Hospital (ULiège CHU), Liège, Belgium. alexandre.szedleski@uliege.be.
None:
We report the case of a 64-year-old woman who developed malignant and treatment-resistant arterial hypertension (HT) following the introduction of rifampicin for spondylodiscitis. Her previously stable blood pressure (BP) deteriorated rapidly despite extensive antihypertensive therapy. The utilisation of pharmaceutical agents that demonstrated minimal or no interaction with rifampicin has yielded only partial control over HT. Furthermore, biological settings provided evidence of pseudohyperaldosteronism. A comprehensive workup ruled out other secondary causes of HT. BP normalized progressively after rifampicin withdrawal, without additional therapeutic intervention. This temporal combination supports a causative role of rifampicin, potentially through mechanisms beyond drug interactions. We discuss hypotheses including corticosterone-driven pseudohyperaldosteronism resulting from cytochrome P450 induction, and pregnane X receptor agonism as contributors to HT. This case highlights the importance of recognizing rifampicin as a potential inducer of severe HT, even in patients receiving adjusted antihypertensive regimens, and suggests a pathophysiological mechanism that may extend beyond pharmacokinetic interferences.
Related Concept Videos
Treatment for Pulmonary Arterial Hypertension: Receptor Tyrosine Kinase Inhibitors and Calcium Channel Blockers
TKIs, such as imatinib (Gleevec), are particularly effective in tackling the growth and mitogenic factors that become upregulated in PAH patients. These factors contribute to the...
Antihypertensive Drugs: Potassium-Sparing Diuretics
Hypertension II: Pathophysiology
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System
Antihypertensive Drugs: Direct Renin Inhibitors
Hormonal Regulation

