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Melatonin for the treatment of gastroesophageal reflux disease; protocol for a systematic review and meta-analysis

BACKGROUND: Melatonin generated in the gastrointestinal tract has mucosal protective effect with inhibiting gastric acid secretion, while increasing gastrin release, which in turn stimulates the contractility of lower esophageal sphincter. Gastroesophageal reflux disease (GERD) is also known to have...

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Autores principales: Bang, Chang Seok, Yang, Young Joo, Baik, Gwang Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6358381/
https://www.ncbi.nlm.nih.gov/pubmed/30681611
http://dx.doi.org/10.1097/MD.0000000000014241
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author Bang, Chang Seok
Yang, Young Joo
Baik, Gwang Ho
author_facet Bang, Chang Seok
Yang, Young Joo
Baik, Gwang Ho
author_sort Bang, Chang Seok
collection PubMed
description BACKGROUND: Melatonin generated in the gastrointestinal tract has mucosal protective effect with inhibiting gastric acid secretion, while increasing gastrin release, which in turn stimulates the contractility of lower esophageal sphincter. Gastroesophageal reflux disease (GERD) is also known to have association with sleep disturbance. However, melatonin or melatonin receptor agonist has not been included in the treatment of GERD. This study aimed to evaluate the efficacy of melatonin for the treatment of GERD. METHODS: We will search the core databases [MEDLINE (through PubMed), the Cochrane Library, and Embase] from their inception to December 2018 by 2 independent evaluators. The P.I.C.O. is as follows; Patients: who have GERD, Intervention: melatonin or melatonin receptor agonist treatment, Comparison: patients without melatonin or melatonin receptor agonist treatment, Outcome: clinical indices (or crude number or proportion of improvement) for the evaluation of symptomatic improvement which enable comparison of efficacy between patients with melatonin or melatonin receptor agonist and the control group. All types of study design will be sought with full-text will be included. The risk of bias will be assessed using the ROBINS-I tool. Descriptive data synthesis is planned and quantitative synthesis will be used if the included studies are sufficiently homogenous. Publication bias will be assessed with quantitative analyses if more than 10 articles are enrolled. RESULTS: The results will provide evidence for the efficacy of melatonin or melatonin receptor agonist for the treatment of GERD. CONCLUSION: This study will provide evidence of melatonin or melatonin receptor agonist treatment for GERD.
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spelling pubmed-63583812019-02-15 Melatonin for the treatment of gastroesophageal reflux disease; protocol for a systematic review and meta-analysis Bang, Chang Seok Yang, Young Joo Baik, Gwang Ho Medicine (Baltimore) Research Article BACKGROUND: Melatonin generated in the gastrointestinal tract has mucosal protective effect with inhibiting gastric acid secretion, while increasing gastrin release, which in turn stimulates the contractility of lower esophageal sphincter. Gastroesophageal reflux disease (GERD) is also known to have association with sleep disturbance. However, melatonin or melatonin receptor agonist has not been included in the treatment of GERD. This study aimed to evaluate the efficacy of melatonin for the treatment of GERD. METHODS: We will search the core databases [MEDLINE (through PubMed), the Cochrane Library, and Embase] from their inception to December 2018 by 2 independent evaluators. The P.I.C.O. is as follows; Patients: who have GERD, Intervention: melatonin or melatonin receptor agonist treatment, Comparison: patients without melatonin or melatonin receptor agonist treatment, Outcome: clinical indices (or crude number or proportion of improvement) for the evaluation of symptomatic improvement which enable comparison of efficacy between patients with melatonin or melatonin receptor agonist and the control group. All types of study design will be sought with full-text will be included. The risk of bias will be assessed using the ROBINS-I tool. Descriptive data synthesis is planned and quantitative synthesis will be used if the included studies are sufficiently homogenous. Publication bias will be assessed with quantitative analyses if more than 10 articles are enrolled. RESULTS: The results will provide evidence for the efficacy of melatonin or melatonin receptor agonist for the treatment of GERD. CONCLUSION: This study will provide evidence of melatonin or melatonin receptor agonist treatment for GERD. Wolters Kluwer Health 2019-01-25 /pmc/articles/PMC6358381/ /pubmed/30681611 http://dx.doi.org/10.1097/MD.0000000000014241 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle Research Article
Bang, Chang Seok
Yang, Young Joo
Baik, Gwang Ho
Melatonin for the treatment of gastroesophageal reflux disease; protocol for a systematic review and meta-analysis
title Melatonin for the treatment of gastroesophageal reflux disease; protocol for a systematic review and meta-analysis
title_full Melatonin for the treatment of gastroesophageal reflux disease; protocol for a systematic review and meta-analysis
title_fullStr Melatonin for the treatment of gastroesophageal reflux disease; protocol for a systematic review and meta-analysis
title_full_unstemmed Melatonin for the treatment of gastroesophageal reflux disease; protocol for a systematic review and meta-analysis
title_short Melatonin for the treatment of gastroesophageal reflux disease; protocol for a systematic review and meta-analysis
title_sort melatonin for the treatment of gastroesophageal reflux disease; protocol for a systematic review and meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6358381/
https://www.ncbi.nlm.nih.gov/pubmed/30681611
http://dx.doi.org/10.1097/MD.0000000000014241
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