Kava in the Treatment of Generalized Anxiety Disorder: A Double-Blind, Randomized, Placebo-Controlled Study
Kava (Piper methysticum) is a plant-based medicine, which has been previously shown to reduce anxiety. To date, however, no placebo-controlled trial assessing kava in the treatment of generalized anxiety disorder (GAD) has been completed. A total of 75 participants with GAD and no comorbid mood diso...
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Veröffentlicht in: | Journal of clinical psychopharmacology 2013-10, Vol.33 (5), p.643-648 |
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description | Kava (Piper methysticum) is a plant-based medicine, which has been previously shown to reduce anxiety. To date, however, no placebo-controlled trial assessing kava in the treatment of generalized anxiety disorder (GAD) has been completed. A total of 75 participants with GAD and no comorbid mood disorder were enrolled in a 6-week double-blind trial of an aqueous extract of kava (120/240 mg of kavalactones per day depending on response) versus placebo. γ-Aminobutyric acid (GABA) and noradrenaline transporter polymorphisms were also analyzed as potential pharmacogenetic markers of response. Reduction in anxiety was measured using the Hamilton Anxiety Rating Scale (HAMA) as the primary outcome. Intention-to-treat analysis was performed on 58 participants who met inclusion criteria after an initial 1 week placebo run-in phase. Results revealed a significant reduction in anxiety for the kava group compared with the placebo group with a moderate effect size (P = 0.046, Cohen d = 0.62). Among participants with moderate to severe Diagnostic and Statistical Manual of Mental Disorders-diagnosed GAD, this effect was larger (P = 0.02; d = 0.82). At conclusion of the controlled phase, 26% of the kava group were classified as remitted (HAMA ≤ 7) compared with 6% of the placebo group (P = 0.04). Within the kava group, GABA transporter polymorphisms rs2601126 (P = 0.021) and rs2697153 (P = 0.046) were associated with HAMA reduction. Kava was well tolerated, and aside from more headaches reported in the kava group (P = 0.05), no other significant differences between groups occurred for any other adverse effects, nor for liver function tests. Standardized kava may be a moderately effective short-term option for the treatment of GAD. Furthermore, specific GABA transporter polymorphisms appear to potentially modify anxiolytic response to kava. |
doi_str_mv | 10.1097/JCP.0b013e318291be67 |
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To date, however, no placebo-controlled trial assessing kava in the treatment of generalized anxiety disorder (GAD) has been completed. A total of 75 participants with GAD and no comorbid mood disorder were enrolled in a 6-week double-blind trial of an aqueous extract of kava (120/240 mg of kavalactones per day depending on response) versus placebo. γ-Aminobutyric acid (GABA) and noradrenaline transporter polymorphisms were also analyzed as potential pharmacogenetic markers of response. Reduction in anxiety was measured using the Hamilton Anxiety Rating Scale (HAMA) as the primary outcome. Intention-to-treat analysis was performed on 58 participants who met inclusion criteria after an initial 1 week placebo run-in phase. Results revealed a significant reduction in anxiety for the kava group compared with the placebo group with a moderate effect size (P = 0.046, Cohen d = 0.62). Among participants with moderate to severe Diagnostic and Statistical Manual of Mental Disorders-diagnosed GAD, this effect was larger (P = 0.02; d = 0.82). At conclusion of the controlled phase, 26% of the kava group were classified as remitted (HAMA ≤ 7) compared with 6% of the placebo group (P = 0.04). Within the kava group, GABA transporter polymorphisms rs2601126 (P = 0.021) and rs2697153 (P = 0.046) were associated with HAMA reduction. Kava was well tolerated, and aside from more headaches reported in the kava group (P = 0.05), no other significant differences between groups occurred for any other adverse effects, nor for liver function tests. Standardized kava may be a moderately effective short-term option for the treatment of GAD. Furthermore, specific GABA transporter polymorphisms appear to potentially modify anxiolytic response to kava.</description><identifier>ISSN: 0271-0749</identifier><identifier>EISSN: 1533-712X</identifier><identifier>DOI: 10.1097/JCP.0b013e318291be67</identifier><identifier>PMID: 23635869</identifier><identifier>CODEN: JCPYDR</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Adult ; Adult and adolescent clinical studies ; Anti-Anxiety Agents - adverse effects ; Anti-Anxiety Agents - therapeutic use ; Anxiety Disorders - diagnosis ; Anxiety Disorders - drug therapy ; Anxiety Disorders - genetics ; Anxiety Disorders - psychology ; Anxiety disorders. Neuroses ; Biological and medical sciences ; Chi-Square Distribution ; Double-Blind Method ; Female ; GABA Plasma Membrane Transport Proteins - genetics ; Humans ; Kava ; Male ; Medical sciences ; Miscellaneous ; Neuropharmacology ; Pharmacogenetics ; Pharmacology. Drug treatments ; Phytotherapy ; Piper methysticum ; Plant Extracts - adverse effects ; Plant Extracts - therapeutic use ; Plants, Medicinal ; Polymorphism, Genetic ; Psychiatric Status Rating Scales ; Psychology. Psychoanalysis. Psychiatry ; Psychopathology. Psychiatry ; Time Factors ; Treatment Outcome ; Victoria ; Young Adult</subject><ispartof>Journal of clinical psychopharmacology, 2013-10, Vol.33 (5), p.643-648</ispartof><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c319t-29fb46884212260aa13952167231c35627c6192bfc6d86531f7212ef4fdb168e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27771121$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23635869$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SARRIS, Jerome</creatorcontrib><creatorcontrib>STOUGH, Con</creatorcontrib><creatorcontrib>BOUSMAN, Chad A</creatorcontrib><creatorcontrib>WAHID, Zahra T</creatorcontrib><creatorcontrib>MURRAY, Greg</creatorcontrib><creatorcontrib>TESCHKE, Rolf</creatorcontrib><creatorcontrib>SAVAGE, Karen M</creatorcontrib><creatorcontrib>DOWELL, Ashley</creatorcontrib><creatorcontrib>CHEE NG</creatorcontrib><creatorcontrib>SCHWEITZER, Isaac</creatorcontrib><title>Kava in the Treatment of Generalized Anxiety Disorder: A Double-Blind, Randomized, Placebo-Controlled Study</title><title>Journal of clinical psychopharmacology</title><addtitle>J Clin Psychopharmacol</addtitle><description>Kava (Piper methysticum) is a plant-based medicine, which has been previously shown to reduce anxiety. To date, however, no placebo-controlled trial assessing kava in the treatment of generalized anxiety disorder (GAD) has been completed. A total of 75 participants with GAD and no comorbid mood disorder were enrolled in a 6-week double-blind trial of an aqueous extract of kava (120/240 mg of kavalactones per day depending on response) versus placebo. γ-Aminobutyric acid (GABA) and noradrenaline transporter polymorphisms were also analyzed as potential pharmacogenetic markers of response. Reduction in anxiety was measured using the Hamilton Anxiety Rating Scale (HAMA) as the primary outcome. Intention-to-treat analysis was performed on 58 participants who met inclusion criteria after an initial 1 week placebo run-in phase. Results revealed a significant reduction in anxiety for the kava group compared with the placebo group with a moderate effect size (P = 0.046, Cohen d = 0.62). Among participants with moderate to severe Diagnostic and Statistical Manual of Mental Disorders-diagnosed GAD, this effect was larger (P = 0.02; d = 0.82). At conclusion of the controlled phase, 26% of the kava group were classified as remitted (HAMA ≤ 7) compared with 6% of the placebo group (P = 0.04). Within the kava group, GABA transporter polymorphisms rs2601126 (P = 0.021) and rs2697153 (P = 0.046) were associated with HAMA reduction. Kava was well tolerated, and aside from more headaches reported in the kava group (P = 0.05), no other significant differences between groups occurred for any other adverse effects, nor for liver function tests. Standardized kava may be a moderately effective short-term option for the treatment of GAD. Furthermore, specific GABA transporter polymorphisms appear to potentially modify anxiolytic response to kava.</description><subject>Adult</subject><subject>Adult and adolescent clinical studies</subject><subject>Anti-Anxiety Agents - adverse effects</subject><subject>Anti-Anxiety Agents - therapeutic use</subject><subject>Anxiety Disorders - diagnosis</subject><subject>Anxiety Disorders - drug therapy</subject><subject>Anxiety Disorders - genetics</subject><subject>Anxiety Disorders - psychology</subject><subject>Anxiety disorders. Neuroses</subject><subject>Biological and medical sciences</subject><subject>Chi-Square Distribution</subject><subject>Double-Blind Method</subject><subject>Female</subject><subject>GABA Plasma Membrane Transport Proteins - genetics</subject><subject>Humans</subject><subject>Kava</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Miscellaneous</subject><subject>Neuropharmacology</subject><subject>Pharmacogenetics</subject><subject>Pharmacology. Drug treatments</subject><subject>Phytotherapy</subject><subject>Piper methysticum</subject><subject>Plant Extracts - adverse effects</subject><subject>Plant Extracts - therapeutic use</subject><subject>Plants, Medicinal</subject><subject>Polymorphism, Genetic</subject><subject>Psychiatric Status Rating Scales</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. Psychiatry</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>Victoria</subject><subject>Young Adult</subject><issn>0271-0749</issn><issn>1533-712X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcFu1DAURS0EotPCHyDkDVIXTfGzHTtmN0xLoVSigiKxixznWQQcu9gJ6vTrSdUBJDas3ubce6V3CHkG7BiY0S_PN5fHrGMgUEDDDXSo9AOyglqISgP_8pCsGNdQMS3NHtkv5RtjIDWvH5M9LpSoG2VW5Pt7-9PSIdLpK9KrjHYaMU40eXqGEbMNwy32dB1vBpy29GQoKfeYX9E1PUlzF7B6HYbYH9GPNvZpvIOP6GWwDrtUbVKccgphKfg0zf32CXnkbSj4dHcPyOc3p1ebt9XFh7N3m_VF5QSYqeLGd1I1jeTAuWLWgjA1B6W5ACdqxbVTYHjnneobVQvweiHRS993oBoUB-Twvvc6px8zlqkdh-IwBBsxzaWFWupmeYBk_0elYMu6EmZB5T3qciolo2-v8zDavG2BtXdG2sVI-6-RJfZ8tzB3I_Z_Qr8VLMCLHWCLs8FnG91Q_nJaawAO4heldJK6</recordid><startdate>20131001</startdate><enddate>20131001</enddate><creator>SARRIS, Jerome</creator><creator>STOUGH, Con</creator><creator>BOUSMAN, Chad A</creator><creator>WAHID, Zahra T</creator><creator>MURRAY, Greg</creator><creator>TESCHKE, Rolf</creator><creator>SAVAGE, Karen M</creator><creator>DOWELL, Ashley</creator><creator>CHEE NG</creator><creator>SCHWEITZER, Isaac</creator><general>Lippincott Williams & Wilkins</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7TK</scope></search><sort><creationdate>20131001</creationdate><title>Kava in the Treatment of Generalized Anxiety Disorder: A Double-Blind, Randomized, Placebo-Controlled Study</title><author>SARRIS, Jerome ; STOUGH, Con ; BOUSMAN, Chad A ; WAHID, Zahra T ; MURRAY, Greg ; TESCHKE, Rolf ; SAVAGE, Karen M ; DOWELL, Ashley ; CHEE NG ; SCHWEITZER, Isaac</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c319t-29fb46884212260aa13952167231c35627c6192bfc6d86531f7212ef4fdb168e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adult</topic><topic>Adult and adolescent clinical studies</topic><topic>Anti-Anxiety Agents - adverse effects</topic><topic>Anti-Anxiety Agents - therapeutic use</topic><topic>Anxiety Disorders - diagnosis</topic><topic>Anxiety Disorders - drug therapy</topic><topic>Anxiety Disorders - genetics</topic><topic>Anxiety Disorders - psychology</topic><topic>Anxiety disorders. Neuroses</topic><topic>Biological and medical sciences</topic><topic>Chi-Square Distribution</topic><topic>Double-Blind Method</topic><topic>Female</topic><topic>GABA Plasma Membrane Transport Proteins - genetics</topic><topic>Humans</topic><topic>Kava</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Miscellaneous</topic><topic>Neuropharmacology</topic><topic>Pharmacogenetics</topic><topic>Pharmacology. Drug treatments</topic><topic>Phytotherapy</topic><topic>Piper methysticum</topic><topic>Plant Extracts - adverse effects</topic><topic>Plant Extracts - therapeutic use</topic><topic>Plants, Medicinal</topic><topic>Polymorphism, Genetic</topic><topic>Psychiatric Status Rating Scales</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>Victoria</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SARRIS, Jerome</creatorcontrib><creatorcontrib>STOUGH, Con</creatorcontrib><creatorcontrib>BOUSMAN, Chad A</creatorcontrib><creatorcontrib>WAHID, Zahra T</creatorcontrib><creatorcontrib>MURRAY, Greg</creatorcontrib><creatorcontrib>TESCHKE, Rolf</creatorcontrib><creatorcontrib>SAVAGE, Karen M</creatorcontrib><creatorcontrib>DOWELL, Ashley</creatorcontrib><creatorcontrib>CHEE NG</creatorcontrib><creatorcontrib>SCHWEITZER, Isaac</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><jtitle>Journal of clinical psychopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SARRIS, Jerome</au><au>STOUGH, Con</au><au>BOUSMAN, Chad A</au><au>WAHID, Zahra T</au><au>MURRAY, Greg</au><au>TESCHKE, Rolf</au><au>SAVAGE, Karen M</au><au>DOWELL, Ashley</au><au>CHEE NG</au><au>SCHWEITZER, Isaac</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Kava in the Treatment of Generalized Anxiety Disorder: A Double-Blind, Randomized, Placebo-Controlled Study</atitle><jtitle>Journal of clinical psychopharmacology</jtitle><addtitle>J Clin Psychopharmacol</addtitle><date>2013-10-01</date><risdate>2013</risdate><volume>33</volume><issue>5</issue><spage>643</spage><epage>648</epage><pages>643-648</pages><issn>0271-0749</issn><eissn>1533-712X</eissn><coden>JCPYDR</coden><abstract>Kava (Piper methysticum) is a plant-based medicine, which has been previously shown to reduce anxiety. To date, however, no placebo-controlled trial assessing kava in the treatment of generalized anxiety disorder (GAD) has been completed. A total of 75 participants with GAD and no comorbid mood disorder were enrolled in a 6-week double-blind trial of an aqueous extract of kava (120/240 mg of kavalactones per day depending on response) versus placebo. γ-Aminobutyric acid (GABA) and noradrenaline transporter polymorphisms were also analyzed as potential pharmacogenetic markers of response. Reduction in anxiety was measured using the Hamilton Anxiety Rating Scale (HAMA) as the primary outcome. Intention-to-treat analysis was performed on 58 participants who met inclusion criteria after an initial 1 week placebo run-in phase. Results revealed a significant reduction in anxiety for the kava group compared with the placebo group with a moderate effect size (P = 0.046, Cohen d = 0.62). Among participants with moderate to severe Diagnostic and Statistical Manual of Mental Disorders-diagnosed GAD, this effect was larger (P = 0.02; d = 0.82). At conclusion of the controlled phase, 26% of the kava group were classified as remitted (HAMA ≤ 7) compared with 6% of the placebo group (P = 0.04). Within the kava group, GABA transporter polymorphisms rs2601126 (P = 0.021) and rs2697153 (P = 0.046) were associated with HAMA reduction. Kava was well tolerated, and aside from more headaches reported in the kava group (P = 0.05), no other significant differences between groups occurred for any other adverse effects, nor for liver function tests. Standardized kava may be a moderately effective short-term option for the treatment of GAD. Furthermore, specific GABA transporter polymorphisms appear to potentially modify anxiolytic response to kava.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>23635869</pmid><doi>10.1097/JCP.0b013e318291be67</doi><tpages>6</tpages></addata></record> |
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subjects | Adult Adult and adolescent clinical studies Anti-Anxiety Agents - adverse effects Anti-Anxiety Agents - therapeutic use Anxiety Disorders - diagnosis Anxiety Disorders - drug therapy Anxiety Disorders - genetics Anxiety Disorders - psychology Anxiety disorders. Neuroses Biological and medical sciences Chi-Square Distribution Double-Blind Method Female GABA Plasma Membrane Transport Proteins - genetics Humans Kava Male Medical sciences Miscellaneous Neuropharmacology Pharmacogenetics Pharmacology. Drug treatments Phytotherapy Piper methysticum Plant Extracts - adverse effects Plant Extracts - therapeutic use Plants, Medicinal Polymorphism, Genetic Psychiatric Status Rating Scales Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Time Factors Treatment Outcome Victoria Young Adult |
title | Kava in the Treatment of Generalized Anxiety Disorder: A Double-Blind, Randomized, Placebo-Controlled Study |
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