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Evaluation of the mechanisms of sarcopenia in chronic inflammatory disease: protocol for a prospective cohort study

BACKGROUND: Several chronic inflammatory diseases co-exist with and accelerate sarcopenia (reduction in muscle strength, function and mass) and negatively impact on both morbidity and mortality. There is currently limited research on the extent of sarcopenia in such conditions, how to accurately ass...

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Autores principales: Dhaliwal, Amritpal, Williams, Felicity R., Quinlan, Jonathan I., Allen, Sophie L., Greig, Carolyn, Filer, Andrew, Raza, Karim, Ghosh, Subrata, Lavery, Gareth G., Newsome, Philip N., Choudhary, Surabhi, Breen, Leigh, Armstrong, Matthew J., Elsharkawy, Ahmed M., Lord, Janet M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8665319/
https://www.ncbi.nlm.nih.gov/pubmed/34895316
http://dx.doi.org/10.1186/s13395-021-00282-5
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author Dhaliwal, Amritpal
Williams, Felicity R.
Quinlan, Jonathan I.
Allen, Sophie L.
Greig, Carolyn
Filer, Andrew
Raza, Karim
Ghosh, Subrata
Lavery, Gareth G.
Newsome, Philip N.
Choudhary, Surabhi
Breen, Leigh
Armstrong, Matthew J.
Elsharkawy, Ahmed M.
Lord, Janet M.
author_facet Dhaliwal, Amritpal
Williams, Felicity R.
Quinlan, Jonathan I.
Allen, Sophie L.
Greig, Carolyn
Filer, Andrew
Raza, Karim
Ghosh, Subrata
Lavery, Gareth G.
Newsome, Philip N.
Choudhary, Surabhi
Breen, Leigh
Armstrong, Matthew J.
Elsharkawy, Ahmed M.
Lord, Janet M.
author_sort Dhaliwal, Amritpal
collection PubMed
description BACKGROUND: Several chronic inflammatory diseases co-exist with and accelerate sarcopenia (reduction in muscle strength, function and mass) and negatively impact on both morbidity and mortality. There is currently limited research on the extent of sarcopenia in such conditions, how to accurately assess it and whether there are generic or disease-specific mechanisms driving sarcopenia. Therefore, this study aims to identify potential mechanisms driving sarcopenia within chronic inflammatory disease via a multi-modal approach; in an attempt to help define potential interventions for future use. METHODS: This prospective cohort study will consist of a multi-modal assessment of sarcopenia and its underlying mechanisms. Recruitment will target three chronic inflammatory diseases: chronic liver disease (CLD) (n=50), with a subset of NAFLD (n=20), inflammatory bowel disease (IBD) (n=50) and rheumatoid arthritis (RA) (n=50) both before and after therapeutic intervention. In addition, 20 age and sex matched healthy individuals will be recruited for comparison. Participants will undergo 4 assessment visits at weeks 0, 2, 12 and 24. Visits will consist of the following assessments: blood tests, anthropometrics, functional assessment, quadriceps muscle imaging, actigraphy, quality of life questionnaires, food diary collection and muscle biopsy of the vastus lateralis (at weeks 2 and 24 only). In addition, stool and urine samples will be collected for future microbiome and metabolomics analysis. DISCUSSION: This is the first study to use a multi-modal assessment model to phenotype sarcopenia in these chronic inflammatory diseases. We hope to identify generic as well as disease-specific mechanisms driving sarcopenia. We appreciate that these cohorts do require separate standards of care treatments which limit comparison between groups. ETHICS AND DISSEMINATION: The study is approved by the Health Research Authority - West Midlands Solihull Research Ethics Service Committee Authority (REC reference: 18/WM/0167). Recruitment commenced in January 2019 and will continue until July 2021. The study was halted in March 2020 and again in January 2021 with the COVID-19 pandemic. The findings will be disseminated through peer-reviewed publications and conference presentations. All data will be stored on a secure server. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT04734496
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spelling pubmed-86653192021-12-13 Evaluation of the mechanisms of sarcopenia in chronic inflammatory disease: protocol for a prospective cohort study Dhaliwal, Amritpal Williams, Felicity R. Quinlan, Jonathan I. Allen, Sophie L. Greig, Carolyn Filer, Andrew Raza, Karim Ghosh, Subrata Lavery, Gareth G. Newsome, Philip N. Choudhary, Surabhi Breen, Leigh Armstrong, Matthew J. Elsharkawy, Ahmed M. Lord, Janet M. Skelet Muscle Protocol BACKGROUND: Several chronic inflammatory diseases co-exist with and accelerate sarcopenia (reduction in muscle strength, function and mass) and negatively impact on both morbidity and mortality. There is currently limited research on the extent of sarcopenia in such conditions, how to accurately assess it and whether there are generic or disease-specific mechanisms driving sarcopenia. Therefore, this study aims to identify potential mechanisms driving sarcopenia within chronic inflammatory disease via a multi-modal approach; in an attempt to help define potential interventions for future use. METHODS: This prospective cohort study will consist of a multi-modal assessment of sarcopenia and its underlying mechanisms. Recruitment will target three chronic inflammatory diseases: chronic liver disease (CLD) (n=50), with a subset of NAFLD (n=20), inflammatory bowel disease (IBD) (n=50) and rheumatoid arthritis (RA) (n=50) both before and after therapeutic intervention. In addition, 20 age and sex matched healthy individuals will be recruited for comparison. Participants will undergo 4 assessment visits at weeks 0, 2, 12 and 24. Visits will consist of the following assessments: blood tests, anthropometrics, functional assessment, quadriceps muscle imaging, actigraphy, quality of life questionnaires, food diary collection and muscle biopsy of the vastus lateralis (at weeks 2 and 24 only). In addition, stool and urine samples will be collected for future microbiome and metabolomics analysis. DISCUSSION: This is the first study to use a multi-modal assessment model to phenotype sarcopenia in these chronic inflammatory diseases. We hope to identify generic as well as disease-specific mechanisms driving sarcopenia. We appreciate that these cohorts do require separate standards of care treatments which limit comparison between groups. ETHICS AND DISSEMINATION: The study is approved by the Health Research Authority - West Midlands Solihull Research Ethics Service Committee Authority (REC reference: 18/WM/0167). Recruitment commenced in January 2019 and will continue until July 2021. The study was halted in March 2020 and again in January 2021 with the COVID-19 pandemic. The findings will be disseminated through peer-reviewed publications and conference presentations. All data will be stored on a secure server. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT04734496 BioMed Central 2021-12-11 /pmc/articles/PMC8665319/ /pubmed/34895316 http://dx.doi.org/10.1186/s13395-021-00282-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Protocol
Dhaliwal, Amritpal
Williams, Felicity R.
Quinlan, Jonathan I.
Allen, Sophie L.
Greig, Carolyn
Filer, Andrew
Raza, Karim
Ghosh, Subrata
Lavery, Gareth G.
Newsome, Philip N.
Choudhary, Surabhi
Breen, Leigh
Armstrong, Matthew J.
Elsharkawy, Ahmed M.
Lord, Janet M.
Evaluation of the mechanisms of sarcopenia in chronic inflammatory disease: protocol for a prospective cohort study
title Evaluation of the mechanisms of sarcopenia in chronic inflammatory disease: protocol for a prospective cohort study
title_full Evaluation of the mechanisms of sarcopenia in chronic inflammatory disease: protocol for a prospective cohort study
title_fullStr Evaluation of the mechanisms of sarcopenia in chronic inflammatory disease: protocol for a prospective cohort study
title_full_unstemmed Evaluation of the mechanisms of sarcopenia in chronic inflammatory disease: protocol for a prospective cohort study
title_short Evaluation of the mechanisms of sarcopenia in chronic inflammatory disease: protocol for a prospective cohort study
title_sort evaluation of the mechanisms of sarcopenia in chronic inflammatory disease: protocol for a prospective cohort study
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8665319/
https://www.ncbi.nlm.nih.gov/pubmed/34895316
http://dx.doi.org/10.1186/s13395-021-00282-5
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