Kava for the Treatment of Generalized Anxiety Disorder RCT: Analysis of Adverse Reactions, Liver Function, Addiction, and Sexual Effects

被引:32
作者
Sarris, J. [1 ,2 ,3 ]
Stough, C. [2 ,3 ]
Teschke, R. [4 ]
Wahid, Z. T. [2 ,3 ]
Bousman, C. A. [1 ,2 ,5 ,6 ]
Murray, G. [7 ]
Savage, K. M. [2 ,3 ]
Mouatt, P. [8 ]
Ng, C. [1 ]
Schweitzer, I. [1 ]
机构
[1] Univ Melbourne, Dept Psychiat, Melbourne, Vic, Australia
[2] Swinburne Univ Technol, Ctr Human Psychopharmacol, Hawthorn, Vic 3122, Australia
[3] NICM Collaborat Ctr Neurocognit, Melbourne, Vic, Australia
[4] Goethe Univ Frankfurt, Teaching Hosp Hanau, Dept Internal Med 2, D-60054 Frankfurt, Germany
[5] Florey Inst Neurosci & Mental Hlth, Melbourne, Vic, Australia
[6] Univ Melbourne, Dept Gen Practice, Melbourne, Vic, Australia
[7] Swinburne Univ Technol, Brain & Psychol Sci Res Ctr, Hawthorn, Vic 3122, Australia
[8] So Cross Univ, So Cross Plant Sci, Lismore, NSW 2480, Australia
基金
英国医学研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
safety; liver function; sexual function; anxiety; kava; Piper methysticum; PIPER-METHYSTICUM; HEPATOTOXICITY;
D O I
10.1002/ptr.4916
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Presently, little is known about a number issues concerning kava (Piper methysticum), including (i) whether kava has any withdrawal or addictive effects; (ii) if genetic polymorphisms of the cytochrome (CYP) P450 2D6 liver enzyme moderates any potential adverse effects; and (iii) if medicinal application of kava has any negative or beneficial effect on sexual function and experience. The study design was a 6-week, double-blind, randomized controlled trial (n=75) involving chronic administration of kava (one tablet of kava twice per day; 120mg of kavalactones per day, titrated in non-response to two tablets of kava twice per day; 240mg of kavalactones) or placebo for participants with generalized anxiety disorder. Results showed no significant differences across groups for liver function tests, nor were there any significant adverse reactions that could be attributed to kava. No differences in withdrawal or addiction were found between groups. Interesting, kava significantly increased female's sexual drive compared to placebo (p=0.040) on a sub-domain of the Arizona Sexual Experience Scale (ASEX), with no negative effects seen in males. Further, it was found that there was a highly significant correlation between ASEX reduction (improved sexual function and performance) and anxiety reduction in the whole sample. Copyright (c) 2013 John Wiley & Sons, Ltd.
引用
收藏
页码:1723 / 1728
页数:6
相关论文
共 24 条
  • [1] Dietary and botanical anxiolytics
    Alramadhan, Elham
    Hanna, Mirna S.
    Hanna, Mena S.
    Goldstein, Todd A.
    Avila, Samantha M.
    Weeks, Benjamin S.
    [J]. MEDICAL SCIENCE MONITOR, 2012, 18 (04): : RA40 - RA48
  • [2] [Anonymous], 2003, Cochrane Database Syst. Rev, DOI DOI 10.1002/14651858.CD003383
  • [3] Bauer R, 2003, PLANTA MED, V69, P971, DOI 10.1055/s-2003-45140
  • [4] AN INVENTORY FOR MEASURING CLINICAL ANXIETY - PSYCHOMETRIC PROPERTIES
    BECK, AT
    BROWN, G
    EPSTEIN, N
    STEER, RA
    [J]. JOURNAL OF CONSULTING AND CLINICAL PSYCHOLOGY, 1988, 56 (06) : 893 - 897
  • [5] Kava kava: examining new reports of toxicity
    Clouatre, DL
    [J]. TOXICOLOGY LETTERS, 2004, 150 (01) : 85 - 96
  • [6] Coulter D., 2007, ASSESSMENT RISK HEPA
  • [7] THE ASSESSMENT OF ANXIETY-STATES BY RATING
    HAMILTON, M
    [J]. BRITISH JOURNAL OF MEDICAL PSYCHOLOGY, 1959, 32 (01): : 50 - 55
  • [8] Liver Function Tests: Their Role in the Diagnosis of Hepatobiliary Diseases
    Knight, Joseph A.
    [J]. JOURNAL OF INFUSION NURSING, 2005, 28 (02) : 108 - 117
  • [9] Neurocognitive effects of kava (Piper methysticum): a systematic review
    LaPorte, E.
    Sarris, J.
    Stough, C.
    Scholey, A.
    [J]. HUMAN PSYCHOPHARMACOLOGY-CLINICAL AND EXPERIMENTAL, 2011, 26 (02) : 102 - 111
  • [10] The Arizona Sexual Experience Scale (ASEX): Reliability and validity
    McGahuey, CA
    Gelenberg, AJ
    Laukes, CA
    Moreno, FA
    Delgado, PL
    McKnight, KM
    Manber, R
    [J]. JOURNAL OF SEX & MARITAL THERAPY, 2000, 26 (01) : 25 - 40