Nutritional therapy in amyotrophic lateral sclerosis: protocol for a systematic review and meta-analysis
- PMID: 36008057
- PMCID: PMC9422859
- DOI: 10.1136/bmjopen-2022-064086
Nutritional therapy in amyotrophic lateral sclerosis: protocol for a systematic review and meta-analysis
Abstract
Introduction: Amyotrophic lateral sclerosis (ALS) is a complex neurodegenerative disease characterised by the degeneration of motor neurons. Nutritional interventions in ALS are essential and must be based on scientific evidence to provide quality of healthcare, improve the quality of life and increase survival time. Therefore, this protocol of systematic reviews and meta-analyses aims to present a synthesis of evidence-based recommendations to support adequate nutrition therapy for patients with ALS.
Methods and analysis: The search will be performed using the following databases: PubMed, Excerpta Medica Database (Embase), Scopus, SciELO, Web of Science, LILACS, Cochrane Central Register of Controlled Trials (CENTRAL), ScienceDirect, ProQuest and Google Scholar. We will include clinical practice guidelines, treatment protocols, systematic reviews and clinical trials according to the three research questions to be answered related to nutrition therapy and interventions in patients with ALS. This protocol will be developed in accordance with the Preferred Reporting Items for Systematic Review and Meta-analysis Protocols. To evaluate the methodological quality of the studies, Appraisal of Guidelines, Research and Evaluation II, Cochrane Risk of Bias 2.0 and Risk of Bias In Non-randomized Studies of Interventions (ROBINS-I) tools will be used. In addition, the Grading of Recommendations Assessment, Development and Evaluation will be used to assess the quality of evidence and the strength of the recommendations. The findings will be summarised and presented descriptively according to the Cochrane Collaboration Handbook and the standard statistical meta-analysis techniques.
Ethics and dissemination: Ethical approval and human consent are not required because this is a protocol for systematic review and only secondary data will be used. Findings will be published in a peer-reviewed journal and presented at conferences. In case of any changes in this protocol, amendments will be updated in International Prospective Register of Systematic Reviews (PROSPERO) and the modifications will be explained in the final report of this review.
Prospero registration number: CRD42021233088.
Keywords: NUTRITION & DIETETICS; Neuromuscular disease; Protocols & guidelines.
© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
Conflict of interest statement
Competing interests: None declared.
Similar articles
-
The future of Cochrane Neonatal.Early Hum Dev. 2020 Nov;150:105191. doi: 10.1016/j.earlhumdev.2020.105191. Epub 2020 Sep 12. Early Hum Dev. 2020. PMID: 33036834
-
Effects of respiratory physiotherapy in patients with amyotrophic lateral sclerosis: protocol for a systematic review of randomised controlled trials.BMJ Open. 2022 May 30;12(5):e061624. doi: 10.1136/bmjopen-2022-061624. BMJ Open. 2022. PMID: 35636801 Free PMC article.
-
Extended reality as a health education strategy of adolescents at school: protocol for systematic review and meta-analysis.BMJ Open. 2023 Jul 4;13(7):e072438. doi: 10.1136/bmjopen-2023-072438. BMJ Open. 2023. PMID: 37407033 Free PMC article.
-
Non-pharmacological strategies for self-directed and interpersonal violence in people with severe mental illness: a rapid overview of systematic reviews.BMJ Open. 2021 Jan 11;11(1):e043576. doi: 10.1136/bmjopen-2020-043576. BMJ Open. 2021. PMID: 33431494 Free PMC article. Review.
-
Protocol for systematic reviews of school-based food and nutrition education intervention for adolescent health promotion: Evidence mapping and syntheses.Medicine (Baltimore). 2019 Aug;98(35):e16977. doi: 10.1097/MD.0000000000016977. Medicine (Baltimore). 2019. PMID: 31464944 Free PMC article.
Cited by
-
Manual Therapy of Dysphagia in a Patient with Amyotrophic Lateral Sclerosis: A Case Report.Medicina (Kaunas). 2024 May 22;60(6):845. doi: 10.3390/medicina60060845. Medicina (Kaunas). 2024. PMID: 38929462 Free PMC article.
-
Evidence-Based Nutritional Recommendations for Maintaining or Restoring Nutritional Status in Patients with Amyotrophic Lateral Sclerosis: A Systematic Review.Nutrients. 2025 Feb 24;17(5):782. doi: 10.3390/nu17050782. Nutrients. 2025. PMID: 40077653 Free PMC article.
-
Neurofilament Light Chain Levels, Skeletal Muscle Loss, and Nutritional Decline: Key Prognostic Factors in Amyotrophic Lateral Sclerosis.Muscle Nerve. 2025 Jul;72(1):49-55. doi: 10.1002/mus.28407. Epub 2025 Apr 4. Muscle Nerve. 2025. PMID: 40183173 Free PMC article.
-
Biochemical parameters as a tool to assess the nutritional status of patients with amyotrophic lateral sclerosis.Front Neurol. 2024 Jan 15;14:1258224. doi: 10.3389/fneur.2023.1258224. eCollection 2023. Front Neurol. 2024. PMID: 38313408 Free PMC article.
-
Data Report: Educational pathway addressing food and nutrition in amyotrophic lateral sclerosis on the AVASUS platform.Front Digit Health. 2025 Jan 6;6:1476293. doi: 10.3389/fdgth.2024.1476293. eCollection 2024. Front Digit Health. 2025. PMID: 39834841 Free PMC article. No abstract available.
References
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous