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Protein Intake and Disability Trajectories in Very Old Adults: The Newcastle 85+ Study

OBJECTIVES: To determine whether protein intake is associated with better disability trajectories in the oldest adults (≥85) and whether muscle mass and muscle strength would partially mediate this. DESIGN: Prospective cohort study. SETTING: Newcastle‐upon‐Tyne and North Tyneside, United Kingdom. PA...

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Autores principales: Mendonça, Nuno, Granic, Antoneta, Hill, Tom R., Siervo, Mario, Mathers, John C., Kingston, Andrew, Jagger, Carol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6334273/
https://www.ncbi.nlm.nih.gov/pubmed/30382594
http://dx.doi.org/10.1111/jgs.15592
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author Mendonça, Nuno
Granic, Antoneta
Hill, Tom R.
Siervo, Mario
Mathers, John C.
Kingston, Andrew
Jagger, Carol
author_facet Mendonça, Nuno
Granic, Antoneta
Hill, Tom R.
Siervo, Mario
Mathers, John C.
Kingston, Andrew
Jagger, Carol
author_sort Mendonça, Nuno
collection PubMed
description OBJECTIVES: To determine whether protein intake is associated with better disability trajectories in the oldest adults (≥85) and whether muscle mass and muscle strength would partially mediate this. DESIGN: Prospective cohort study. SETTING: Newcastle‐upon‐Tyne and North Tyneside, United Kingdom. PARTICIPANTS: Community‐dwelling older adults aged 85 at baseline (N=722). METHODS: Protein intake was estimated using two 24‐hour multiple‐pass recalls at baseline. Disability was measured as difficulty performing 17 activities of daily living at baseline and 18, 36, and 60 months. Trajectories were derived using mortality‐adjusted group‐based trajectory modelling. The effect of protein intake (g/kg of adjusted body weight (aBW)/d) on disability trajectories was examined using multinomial logistic regression. RESULTS: Participants had 4 distinct disability trajectories (between the ages of 85 and 90: constant very low (AT1), mild (AT2), moderate (AT3), and severe (AT4). Each unit increase in protein (g) per kg of aBW/d was associated with greater odds of AT1 (odds ratio (OR=7.97, 95% confidence interval (CI)=1.96–32.43, p = .004) and AT2 (OR=3.28, 95% CI=1.09–9.87, p = .03) than of AT4 over 5 years in models adjusted for selected covariates. Participants with protein intake of 1.0 g/kg aBW/d or more were more likely to belong to AT1 (OR=3.65, 95% CI=1.59–8.38, p = .009) and AT2 (OR=2.12, 95% CI=1.16–3.90, p = .01) than to AT4. CONCLUSION: Higher protein intake, especially 1.0 g/kg aBW/d or more, was associated with better disability trajectories in the oldest adults. These findings will inform new dietary strategies to support active, healthy ageing. J Am Geriatr Soc 67:50–56, 2019.
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spelling pubmed-63342732019-01-23 Protein Intake and Disability Trajectories in Very Old Adults: The Newcastle 85+ Study Mendonça, Nuno Granic, Antoneta Hill, Tom R. Siervo, Mario Mathers, John C. Kingston, Andrew Jagger, Carol J Am Geriatr Soc Clinical Investigations OBJECTIVES: To determine whether protein intake is associated with better disability trajectories in the oldest adults (≥85) and whether muscle mass and muscle strength would partially mediate this. DESIGN: Prospective cohort study. SETTING: Newcastle‐upon‐Tyne and North Tyneside, United Kingdom. PARTICIPANTS: Community‐dwelling older adults aged 85 at baseline (N=722). METHODS: Protein intake was estimated using two 24‐hour multiple‐pass recalls at baseline. Disability was measured as difficulty performing 17 activities of daily living at baseline and 18, 36, and 60 months. Trajectories were derived using mortality‐adjusted group‐based trajectory modelling. The effect of protein intake (g/kg of adjusted body weight (aBW)/d) on disability trajectories was examined using multinomial logistic regression. RESULTS: Participants had 4 distinct disability trajectories (between the ages of 85 and 90: constant very low (AT1), mild (AT2), moderate (AT3), and severe (AT4). Each unit increase in protein (g) per kg of aBW/d was associated with greater odds of AT1 (odds ratio (OR=7.97, 95% confidence interval (CI)=1.96–32.43, p = .004) and AT2 (OR=3.28, 95% CI=1.09–9.87, p = .03) than of AT4 over 5 years in models adjusted for selected covariates. Participants with protein intake of 1.0 g/kg aBW/d or more were more likely to belong to AT1 (OR=3.65, 95% CI=1.59–8.38, p = .009) and AT2 (OR=2.12, 95% CI=1.16–3.90, p = .01) than to AT4. CONCLUSION: Higher protein intake, especially 1.0 g/kg aBW/d or more, was associated with better disability trajectories in the oldest adults. These findings will inform new dietary strategies to support active, healthy ageing. J Am Geriatr Soc 67:50–56, 2019. John Wiley and Sons Inc. 2018-11-01 2019-01 /pmc/articles/PMC6334273/ /pubmed/30382594 http://dx.doi.org/10.1111/jgs.15592 Text en © 2018 The Authors. Journal of the American Geriatrics Society published by Wiley Periodicals, Inc. on behalf of The American Geriatrics Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Investigations
Mendonça, Nuno
Granic, Antoneta
Hill, Tom R.
Siervo, Mario
Mathers, John C.
Kingston, Andrew
Jagger, Carol
Protein Intake and Disability Trajectories in Very Old Adults: The Newcastle 85+ Study
title Protein Intake and Disability Trajectories in Very Old Adults: The Newcastle 85+ Study
title_full Protein Intake and Disability Trajectories in Very Old Adults: The Newcastle 85+ Study
title_fullStr Protein Intake and Disability Trajectories in Very Old Adults: The Newcastle 85+ Study
title_full_unstemmed Protein Intake and Disability Trajectories in Very Old Adults: The Newcastle 85+ Study
title_short Protein Intake and Disability Trajectories in Very Old Adults: The Newcastle 85+ Study
title_sort protein intake and disability trajectories in very old adults: the newcastle 85+ study
topic Clinical Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6334273/
https://www.ncbi.nlm.nih.gov/pubmed/30382594
http://dx.doi.org/10.1111/jgs.15592
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