Effect of kava (Piper methysticum) on peripheral gene expression among individuals with generalized anxiety disorder: A post hoc analysis of a randomized controlled trial

Author:

Cribb Lachlan1ORCID,Sarris Jerome23ORCID,Savage Karen M.4ORCID,Byrne Gerard J.45,Metri Najwa‐Joelle2,Scholey Andrew6,Stough Con6,Bousman Chad A.78

Affiliation:

1. Professorial Unit, The Melbourne Clinic, Department of Psychiatry The University of Melbourne Parkville Victoria Australia

2. NICM Health Research Institute Western Sydney University Westmead New South Wales Australia

3. Florey Institute of Neuroscience and Mental Health The University of Melbourne Parkville Victoria Australia

4. Department of Psychiatry ACT Health Canberra Australia

5. School of Clinical Medicine, Discipline of Psychiatry The University of Queensland Queensland Australia

6. Centre for Human Psychopharmacology Hawthorn, Swinburne University of Technology Victoria Australia

7. Department of Medical Genetics Psychiatry, Physiology & Pharmacology Calgary Alberta Canada

8. Department of Psychiatry Parkville Victoria Australia

Abstract

AbstractKava is a South Pacific plant‐based medicine with anxiolytic properties, but little is known about the impact kava has on gene expression or whether gene expression can serve as a marker of kava response. This study aimed to determine whether kava treatment alters the expression of genes with physiological relevance to anxiety pathophysiology and whether the baseline expression of these physiologically relevant genes modifies the efficacy of kava treatment. In this post hoc analysis, we examined the expression of 48 genes relevant to the pathophysiology of anxiety collected from a double‐blind randomized controlled trial that assessed the efficacy of kava treatment in generalized anxiety disorder. Peripheral blood gene expression was measured in 71 (34 kava, 37 placebo) adults at baseline and in 40 (19 kava, 21 placebo) after 8 weeks of treatment by reverse transcription polymerase chain reaction (PCR). Results revealed that kava decreased the expression of a subunit of the GABAA‐rho receptor gene (GABRR2) and catechol‐O‐methyltransferase (COMT), a gene related to catecholamine metabolism. Kava efficacy was not found to be modified by baseline (pretreatment) expression of relevant genes. Although these results did not withstand statistical correction for multiple comparisons and require external validation, they support the notion that kava's mechanism of action includes interaction with GABAergic and catecholaminergic systems.

Funder

National Health and Medical Research Council

Publisher

Wiley

Subject

Pharmacology

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1. ANXIOLYTICS: Origins, drug discovery, and mechanisms;Pharmacology Biochemistry and Behavior;2024-12

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