Neil Williams
Prebiotics for people with cystic fibrosis
Williams, Neil; Jayaratnasingam, Jacob; Prayle, Andrew P; Nevitt, Sarah J; Smyth, Alan R
Authors
Jacob Jayaratnasingam
ANDREW PRAYLE andrew.prayle@nottingham.ac.uk
Clinical Associate Professor
Sarah J Nevitt
Alan R Smyth
Abstract
Background. Description of the condition. Cystic fibrosis (CF) is a life‐limiting genetic disease caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. It affects approximately 100,000 children and adults worldwide (Bell 2020). CF is a multisystem disease resulting in thick secretions predominantly affecting the lungs, gastrointestinal (GI) tract, pancreas and liver. Around 84% of people with CF have exocrine pancreatic insufficiency, requiring treatment with pancreatic enzyme replacement therapy (PERT) (Cystic Fibrosis Foundation Patient Registry 2020). In spite of treatment with PERT, many people have frequent GI symptoms (Smith 2020). Children with CF may struggle to gain weight adequately and adults may have difficulty maintaining a healthy weight (Stallings 2008). The growth and nutritional status of people with CF is important as they are major determinants of lung function and survival (Corey 1988; Jadin 2011). Around half of people with CF achieve an adequate nutritional status (McCormick 2010; Turck 2016); and many children with CF fail to achieve catch‐up weight gain. However, a new era of CF care has increased lifespan and decreased symptoms in many people with CF, necessitating a re‐examination of the legacy diets in CF (McDonald 2021).
Citation
Williams, N., Jayaratnasingam, J., Prayle, A. P., Nevitt, S. J., & Smyth, A. R. (2022). Prebiotics for people with cystic fibrosis. Cochrane Database of Systematic Reviews, 2022(12), Article CD015236. https://doi.org/10.1002/14651858.cd015236
Journal Article Type | Review |
---|---|
Acceptance Date | Dec 16, 2022 |
Online Publication Date | Dec 16, 2022 |
Publication Date | Dec 16, 2022 |
Deposit Date | Apr 22, 2023 |
Publicly Available Date | Dec 17, 2023 |
Journal | Cochrane Database of Systematic Reviews |
Electronic ISSN | 1469-493X |
Publisher | Cochrane Collaboration |
Peer Reviewed | Peer Reviewed |
Volume | 2022 |
Issue | 12 |
Article Number | CD015236 |
DOI | https://doi.org/10.1002/14651858.cd015236 |
Keywords | Pharmacology (medical) |
Public URL | https://nottingham-repository.worktribe.com/output/15431429 |
Publisher URL | https://www.cochranelibrary.com/cdsr/doi/10.1002/14651858.CD015236/full |
Additional Information | Williams N, Jayaratnasingam J, Prayle AP, Nevitt SJ, Smyth AR. Prebiotics for people with cystic fibrosis (Protocol). Cochrane Database of Systematic Reviews 2022, Issue 12. Art. No.: CD015236. DOI: 10.1002/14651858.CD015236. |
Files
Prebiotics for people with cystic fibrosis
(199 Kb)
PDF
Publisher Licence URL
No License Set (All rights reserved)
Copyright Statement
Copyright © 2022 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd
You might also like
Delayed publications of clinical trials in cystic fibrosis
(2011)
Journal Article
Intravenous antibiotics for pulmonary exacerbations in people with cystic fibrosis
(2015)
Journal Article
Growth and nutrition in children with Ataxia telangiectasia
(2016)
Journal Article
Downloadable Citations
About Repository@Nottingham
Administrator e-mail: discovery-access-systems@nottingham.ac.uk
This application uses the following open-source libraries:
SheetJS Community Edition
Apache License Version 2.0 (http://www.apache.org/licenses/)
PDF.js
Apache License Version 2.0 (http://www.apache.org/licenses/)
Font Awesome
SIL OFL 1.1 (http://scripts.sil.org/OFL)
MIT License (http://opensource.org/licenses/mit-license.html)
CC BY 3.0 ( http://creativecommons.org/licenses/by/3.0/)
Powered by Worktribe © 2024
Advanced Search