Cargando…

The impact of peppermint oil on the irritable bowel syndrome: a meta-analysis of the pooled clinical data

BACKGROUND: Peppermint oil (PO) has intrinsic properties that may benefit patients with irritable bowel syndrome (IBS) symptoms. The study objective was to determine the effect of peppermint oil in the treatment of the IBS. METHODS: We systematically searched MEDLINE (PubMed), Cochrane Central Regis...

Descripción completa

Detalles Bibliográficos
Autores principales: Alammar, N., Wang, L., Saberi, B., Nanavati, J., Holtmann, G., Shinohara, R. T., Mullin, G. E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337770/
https://www.ncbi.nlm.nih.gov/pubmed/30654773
http://dx.doi.org/10.1186/s12906-018-2409-0
_version_ 1783388327115751424
author Alammar, N.
Wang, L.
Saberi, B.
Nanavati, J.
Holtmann, G.
Shinohara, R. T.
Mullin, G. E.
author_facet Alammar, N.
Wang, L.
Saberi, B.
Nanavati, J.
Holtmann, G.
Shinohara, R. T.
Mullin, G. E.
author_sort Alammar, N.
collection PubMed
description BACKGROUND: Peppermint oil (PO) has intrinsic properties that may benefit patients with irritable bowel syndrome (IBS) symptoms. The study objective was to determine the effect of peppermint oil in the treatment of the IBS. METHODS: We systematically searched MEDLINE (PubMed), Cochrane Central Register of Controlled Trials (Cochrane CENTRAL), ClinicalTrials.gov, EMBASE (Ovid), and Web of Science for randomized controlled trials (RCTs) of PO for IBS. We appraised the eligible studies by the Cochrane risk of bias tool. We performed random-effects meta-analysis on primary outcomes including global improvement in IBS symptoms and abdominal pain. A PRISMA-compliant study protocol is registered in PROSPERO Register [2016, CRD42016050917]. RESULTS: Twelve randomized trials with 835 patients were included. For global symptom improvement, the risk ratio (RR) from seven RCTs for the effect of PO (n = 253) versus placebo (n = 254) on global symptoms was 2.39 [95% confidence interval (CI): 1.93, 2.97], I(2) = 0%, z = 7.93 (p < 0.00001). Regarding abdominal pain, the RR from six RCTs for the effect of PO (n = 278) versus placebo (n = 278) was 1.78 [95% CI: 1.43, 2.20], I(2) = 0%, z = 5.23 (p < 0.00001). Overall, there were no differences in the reported adverse effects: PO (32 events, 344 total, 9.3%) versus placebo (20 events, 327 total, 6.1%) for eight RCTs; RR 1.40 [95% CI: 0.87, 2.26] I(2) = 0%, z = 1.39 (p = 0.16). The number needed to treat with PO to prevent one patient from having persistent symptoms was three for global symptoms and four for abdominal pain. CONCLUSIONS: In the most comprehensive meta-analysis to date, PO was shown to be a safe and effective therapy for pain and global symptoms in adults with IBS. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12906-018-2409-0) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6337770
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-63377702019-01-23 The impact of peppermint oil on the irritable bowel syndrome: a meta-analysis of the pooled clinical data Alammar, N. Wang, L. Saberi, B. Nanavati, J. Holtmann, G. Shinohara, R. T. Mullin, G. E. BMC Complement Altern Med Research Article BACKGROUND: Peppermint oil (PO) has intrinsic properties that may benefit patients with irritable bowel syndrome (IBS) symptoms. The study objective was to determine the effect of peppermint oil in the treatment of the IBS. METHODS: We systematically searched MEDLINE (PubMed), Cochrane Central Register of Controlled Trials (Cochrane CENTRAL), ClinicalTrials.gov, EMBASE (Ovid), and Web of Science for randomized controlled trials (RCTs) of PO for IBS. We appraised the eligible studies by the Cochrane risk of bias tool. We performed random-effects meta-analysis on primary outcomes including global improvement in IBS symptoms and abdominal pain. A PRISMA-compliant study protocol is registered in PROSPERO Register [2016, CRD42016050917]. RESULTS: Twelve randomized trials with 835 patients were included. For global symptom improvement, the risk ratio (RR) from seven RCTs for the effect of PO (n = 253) versus placebo (n = 254) on global symptoms was 2.39 [95% confidence interval (CI): 1.93, 2.97], I(2) = 0%, z = 7.93 (p < 0.00001). Regarding abdominal pain, the RR from six RCTs for the effect of PO (n = 278) versus placebo (n = 278) was 1.78 [95% CI: 1.43, 2.20], I(2) = 0%, z = 5.23 (p < 0.00001). Overall, there were no differences in the reported adverse effects: PO (32 events, 344 total, 9.3%) versus placebo (20 events, 327 total, 6.1%) for eight RCTs; RR 1.40 [95% CI: 0.87, 2.26] I(2) = 0%, z = 1.39 (p = 0.16). The number needed to treat with PO to prevent one patient from having persistent symptoms was three for global symptoms and four for abdominal pain. CONCLUSIONS: In the most comprehensive meta-analysis to date, PO was shown to be a safe and effective therapy for pain and global symptoms in adults with IBS. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12906-018-2409-0) contains supplementary material, which is available to authorized users. BioMed Central 2019-01-17 /pmc/articles/PMC6337770/ /pubmed/30654773 http://dx.doi.org/10.1186/s12906-018-2409-0 Text en © The Author(s). 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Alammar, N.
Wang, L.
Saberi, B.
Nanavati, J.
Holtmann, G.
Shinohara, R. T.
Mullin, G. E.
The impact of peppermint oil on the irritable bowel syndrome: a meta-analysis of the pooled clinical data
title The impact of peppermint oil on the irritable bowel syndrome: a meta-analysis of the pooled clinical data
title_full The impact of peppermint oil on the irritable bowel syndrome: a meta-analysis of the pooled clinical data
title_fullStr The impact of peppermint oil on the irritable bowel syndrome: a meta-analysis of the pooled clinical data
title_full_unstemmed The impact of peppermint oil on the irritable bowel syndrome: a meta-analysis of the pooled clinical data
title_short The impact of peppermint oil on the irritable bowel syndrome: a meta-analysis of the pooled clinical data
title_sort impact of peppermint oil on the irritable bowel syndrome: a meta-analysis of the pooled clinical data
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337770/
https://www.ncbi.nlm.nih.gov/pubmed/30654773
http://dx.doi.org/10.1186/s12906-018-2409-0
work_keys_str_mv AT alammarn theimpactofpeppermintoilontheirritablebowelsyndromeametaanalysisofthepooledclinicaldata
AT wangl theimpactofpeppermintoilontheirritablebowelsyndromeametaanalysisofthepooledclinicaldata
AT saberib theimpactofpeppermintoilontheirritablebowelsyndromeametaanalysisofthepooledclinicaldata
AT nanavatij theimpactofpeppermintoilontheirritablebowelsyndromeametaanalysisofthepooledclinicaldata
AT holtmanng theimpactofpeppermintoilontheirritablebowelsyndromeametaanalysisofthepooledclinicaldata
AT shinoharart theimpactofpeppermintoilontheirritablebowelsyndromeametaanalysisofthepooledclinicaldata
AT mullinge theimpactofpeppermintoilontheirritablebowelsyndromeametaanalysisofthepooledclinicaldata
AT alammarn impactofpeppermintoilontheirritablebowelsyndromeametaanalysisofthepooledclinicaldata
AT wangl impactofpeppermintoilontheirritablebowelsyndromeametaanalysisofthepooledclinicaldata
AT saberib impactofpeppermintoilontheirritablebowelsyndromeametaanalysisofthepooledclinicaldata
AT nanavatij impactofpeppermintoilontheirritablebowelsyndromeametaanalysisofthepooledclinicaldata
AT holtmanng impactofpeppermintoilontheirritablebowelsyndromeametaanalysisofthepooledclinicaldata
AT shinoharart impactofpeppermintoilontheirritablebowelsyndromeametaanalysisofthepooledclinicaldata
AT mullinge impactofpeppermintoilontheirritablebowelsyndromeametaanalysisofthepooledclinicaldata