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Adaptation and validation of a protein intake screening tool for a UK adult population

Adequate dietary protein intake is important in human subjects for maintaining muscle turnover, determining the protein content of tissues and thus the preservation of muscle mass and function as we age. A screening tool to assess if an older individual is likely to have a lower dietary protein inta...

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Autores principales: Tuttiett, Esme R., Ioannou, Elysa, Wijnhoven, Hanneke A.H., Corfe, Bernard M., Williams, Elizabeth A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9672832/
https://www.ncbi.nlm.nih.gov/pubmed/36405091
http://dx.doi.org/10.1017/jns.2022.96
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author Tuttiett, Esme R.
Ioannou, Elysa
Wijnhoven, Hanneke A.H.
Corfe, Bernard M.
Williams, Elizabeth A.
author_facet Tuttiett, Esme R.
Ioannou, Elysa
Wijnhoven, Hanneke A.H.
Corfe, Bernard M.
Williams, Elizabeth A.
author_sort Tuttiett, Esme R.
collection PubMed
description Adequate dietary protein intake is important in human subjects for maintaining muscle turnover, determining the protein content of tissues and thus the preservation of muscle mass and function as we age. A screening tool to assess if an older individual is likely to have a lower dietary protein intake (predicted probability of protein intake ≤1⋅0 g/kg per d), has been developed for a Netherlands dietary profile, but this has not been validated in a UK population. This study aimed to adapt and then validate the protein screening tool for use in a UK population. Amendment of the tool was undertaken using data from UK BioBank and the UK National Diet and Nutrition Survey to reflect protein sources in the UK diet. Validation of the amended version of the protein screener screening tool was conducted using protein intake derived from a food frequency questionnaire (FFQ) in a sample of UK adults (n = 184) (age range 18–91 years) as the reference standard. Using the FFQ, 40 % of respondents (n = 74) reported a protein intake of ≤1⋅0 g per kg body mass. The discriminative accuracy of the amended screener was tested using receiver operating characteristic (ROC) curves. The area under the curve for the ROC was 0⋅731 (95 % CI 0⋅657, 0⋅805), indicating that the amended screener may be a valid tool to screen for individuals consuming ≤1⋅0 g/kg adjusted BM/d in an adult UK population. This protein screener tool is a potential method to screen individuals with a likelihood of habitually consuming protein intakes of ≤1⋅0 g/kg per d. Further validation is needed using a more robust dietary intake methodology and for specific groups, such as older adults. The screener may be applicable across healthcare, clinical and research applications.
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spelling pubmed-96728322022-11-18 Adaptation and validation of a protein intake screening tool for a UK adult population Tuttiett, Esme R. Ioannou, Elysa Wijnhoven, Hanneke A.H. Corfe, Bernard M. Williams, Elizabeth A. J Nutr Sci Research Article Adequate dietary protein intake is important in human subjects for maintaining muscle turnover, determining the protein content of tissues and thus the preservation of muscle mass and function as we age. A screening tool to assess if an older individual is likely to have a lower dietary protein intake (predicted probability of protein intake ≤1⋅0 g/kg per d), has been developed for a Netherlands dietary profile, but this has not been validated in a UK population. This study aimed to adapt and then validate the protein screening tool for use in a UK population. Amendment of the tool was undertaken using data from UK BioBank and the UK National Diet and Nutrition Survey to reflect protein sources in the UK diet. Validation of the amended version of the protein screener screening tool was conducted using protein intake derived from a food frequency questionnaire (FFQ) in a sample of UK adults (n = 184) (age range 18–91 years) as the reference standard. Using the FFQ, 40 % of respondents (n = 74) reported a protein intake of ≤1⋅0 g per kg body mass. The discriminative accuracy of the amended screener was tested using receiver operating characteristic (ROC) curves. The area under the curve for the ROC was 0⋅731 (95 % CI 0⋅657, 0⋅805), indicating that the amended screener may be a valid tool to screen for individuals consuming ≤1⋅0 g/kg adjusted BM/d in an adult UK population. This protein screener tool is a potential method to screen individuals with a likelihood of habitually consuming protein intakes of ≤1⋅0 g/kg per d. Further validation is needed using a more robust dietary intake methodology and for specific groups, such as older adults. The screener may be applicable across healthcare, clinical and research applications. Cambridge University Press 2022-11-10 /pmc/articles/PMC9672832/ /pubmed/36405091 http://dx.doi.org/10.1017/jns.2022.96 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
spellingShingle Research Article
Tuttiett, Esme R.
Ioannou, Elysa
Wijnhoven, Hanneke A.H.
Corfe, Bernard M.
Williams, Elizabeth A.
Adaptation and validation of a protein intake screening tool for a UK adult population
title Adaptation and validation of a protein intake screening tool for a UK adult population
title_full Adaptation and validation of a protein intake screening tool for a UK adult population
title_fullStr Adaptation and validation of a protein intake screening tool for a UK adult population
title_full_unstemmed Adaptation and validation of a protein intake screening tool for a UK adult population
title_short Adaptation and validation of a protein intake screening tool for a UK adult population
title_sort adaptation and validation of a protein intake screening tool for a uk adult population
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9672832/
https://www.ncbi.nlm.nih.gov/pubmed/36405091
http://dx.doi.org/10.1017/jns.2022.96
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