Effect of a Proposed Cav1.3 Inhibitor in Primary Aldosteronism

Effect of a Proposed Cav1.3 Inhibitor in Primary Aldosteronism - a Pilot Study

The goal of this pilot, open-label prospective study is to evaluate if the effect of calcium channel blockade on plasma aldosterone levels in people with primary aldosteronism (PA) is due primarily to Cav1.3 blockade.

This will be tested by treating participants who have PA with both cinnarizine (Cav1.3 blocker) and nifedipine (Cav1.2 blocker) and evaluating effect on aldosterone levels and blood pressure over a two week course of treatment.

Medical treatment for Primary Aldosteronism (PA) is currently limited to mineralocorticoid receptor antagonists (MRA), the most widely available of which is spironolactone. This can cause numerous adverse effects, especially in men, due to interference with androgen and progesterone signalling. Hence, alternative drug targets are needed, one potential of which is Cav1.3.

The CACNA1D mutation in PA affects the calcium channel Cav1.3. Cav1.3 inhibition may offer targeted treatment for patients with mutations in CACNA1D. Cav1.3 has been a candidate for novel inhibitors of aldosterone production,4 for which the case is enhanced if CACNA1D-mutations underlie the above-described phenotype of PA (asymmetric disease leading to failure to achieve cure with adrenalectomy).

The calcium-channel blocker, cinnarizine, typically used for vertigo and nausea, has been identified to fit the recently described crystal structure of Cav1.3. This raises the possibility of using this drug to assess the effect of Cav1.3 inhibition in PA. This may lead to further studies involving randomisation and placebo to determine if Cav1.3 inhibition is an important method by which aldosterone levels can be lowered in people with PA.

This study seeks to explore whether the effect of calcium channel blockade on aldosterone levels in people with PA is due to Cav1.3 blockade, by comparing cinnarizine (proposed Cav1.3 inhibitor) to a conventional calcium channel blocker nifedipine (Cav1.2 inhibitor). Cinnarizine is not a likely prospect for long-term treatment of PA, because of its potential additional actions as well as Cav1.3 blockade, but using it in this setting, for a short period of time, allows exploration of a property of this existing drug (Cav1.3 inhibition). Outcomes could form the basis of further exploration of this mechanism for future PA treatments.

Inclusion Criteria:

• Confirmed PA, as demonstrated by a positive screening test and internationally endorsed confirmatory test (saline suppression test, captopril challenge test)
• Adults > 18 years of age
• Able and willing to give informed consent

Exclusion Criteria:

• Uncontrolled hypertension requiring use of MRA
• Unwilling or unable to give consent
• Below age 18 or above age 90 years
• Allergy to cinnarizine or nifedipine or their excipients
• Existing use of cinnarizine or nifedipine for an alternative indication
• Breastfeeding or pregnant women
• Diagnosis of Parkinson's disease
• Severe hepatic or renal insufficiency
• Concurrent use of sedating central nervous system (CNS) depressants or rifampicin
• Porphyria
• Cardiogenic shock, clinically significant aortic stenosis, unstable angina, within one month of a myocardial infarction
• Previous gastro-intestinal or oesophageal obstruction or ileostomy