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Kava for generalised anxiety disorder: A 16-week double-blind, randomised, placebo-controlled study.
- Source :
-
The Australian and New Zealand journal of psychiatry [Aust N Z J Psychiatry] 2020 Mar; Vol. 54 (3), pp. 288-297. Date of Electronic Publication: 2019 Dec 08. - Publication Year :
- 2020
-
Abstract
- Objective: Previous randomised, double-blind, placebo-controlled studies have shown that Kava (a South Pacific medicinal plant) reduced anxiety during short-term administration. The objective of this randomised, double-blind, placebo-controlled study was to perform a larger, longer-term trial assessing the efficacy and safety of Kava in the treatment of generalised anxiety disorder and to determine whether gamma-aminobutyric acid transporter (SLC6A1) single-nucleotide polymorphisms were moderators of response.<br />Methods: The trial was a phase III, multi-site, two-arm, 16-week, randomised, double-blind, placebo-controlled study investigating an aqueous extract of dried Kava root administered twice per day in tablet form (standardised to 120 mg of kavalactones twice/day) in 171 currently non-medicated anxious participants with diagnosed generalised anxiety disorder. The trial took place in Australia.<br />Results: An analysis of 171 participants revealed a non-significant difference in anxiety reduction between the Kava and placebo groups (a relative reduction favouring placebo of 1.37 points; p = 0.25). At the conclusion of the controlled phase, 17.4% of the Kava group were classified as remitted (Hamilton Anxiety Rating Scale score < 7) compared to 23.8% of the placebo group ( p = 0.46). No SLC6A1 polymorphisms were associated with treatment response, while carriers of the rs2601126 T allele preferentially respond to placebo ( p = 0.006). Kava was well tolerated aside from poorer memory (Kava = 36 vs placebo = 23; p = 0.044) and tremor/shakiness (Kava = 36 vs placebo = 23; p = 0.024) occurring more frequently in the Kava group. Liver function test abnormalities were significantly more frequent in the Kava group, although no participant met criteria for herb-induced hepatic injury.<br />Conclusion: While research has generally supported Kava in non-clinical populations (potentially for more 'situational' anxiety as a short-term anxiolytic), this particular extract was not effective for diagnosed generalised anxiety disorder.
- Subjects :
- Adult
Anti-Anxiety Agents adverse effects
Anxiety Disorders genetics
Australia
Double-Blind Method
Female
GABA Plasma Membrane Transport Proteins genetics
Humans
Male
Middle Aged
Phytotherapy
Plant Extracts adverse effects
Plant Roots chemistry
Polymorphism, Single Nucleotide
Psychiatric Status Rating Scales
Time Factors
Treatment Outcome
Young Adult
Anti-Anxiety Agents therapeutic use
Anxiety Disorders drug therapy
Kava chemistry
Plant Extracts therapeutic use
Subjects
Details
- Language :
- English
- ISSN :
- 1440-1614
- Volume :
- 54
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- The Australian and New Zealand journal of psychiatry
- Publication Type :
- Academic Journal
- Accession number :
- 31813230
- Full Text :
- https://doi.org/10.1177/0004867419891246