Trials (Feb 2019)

The Oxford study of Calcium channel Antagonism, Cognition, Mood instability and Sleep (OxCaMS): study protocol for a randomised controlled, experimental medicine study

  • Lauren Z. Atkinson,
  • Lucy Colbourne,
  • Alexander Smith,
  • Catherine H. Harmer,
  • Anna C. Nobre,
  • Jennifer Rendell,
  • Helen Jones,
  • Christopher Hinds,
  • Arne Mould,
  • Elizabeth M. Tunbridge,
  • Andrea Cipriani,
  • John R. Geddes,
  • Kate E. A. Saunders,
  • Paul J. Harrison

DOI
https://doi.org/10.1186/s13063-019-3175-0
Journal volume & issue
Vol. 20, no. 1
pp. 1 – 11

Abstract

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Abstract Background The discovery that voltage-gated calcium channel genes such as CACNA1C are part of the aetiology of psychiatric disorders has rekindled interest in the therapeutic potential of L-type calcium channel (LTCC) antagonists. These drugs, licensed to treat hypertension and angina, have previously been used in bipolar disorder, but without clear results. Neither is much known about the broader effects of these drugs on the brain and behaviour. Methods The Oxford study of Calcium channel Antagonism, Cognition, Mood instability and Sleep (OxCaMS) is a high-intensity randomised, double-blind, placebo-controlled experimental medicine study on the effect of the LTCC antagonist nicardipine in healthy young adults with mood instability. An array of cognitive, psychiatric, circadian, physiological, biochemical and neuroimaging (functional magnetic resonance imaging and magnetoencephalography) parameters are measured during a 4-week period, with randomisation to drug or placebo on day 14. We are interested in whether nicardipine affects the stability of these measures, as well as its overall effects. Participants are genotyped for the CACNA1C risk polymorphism rs1006737. Discussion The results will clarify the potential of LTCC antagonists for repurposing or modification for use in psychiatric disorders in which cognition, mood and sleep are affected. Trial registration ISRCTN, ISRCTN33631053. Retrospectively registered on 8 June 2018 (applied 17 May 2018).

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