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Higher dietary protein intake is associated with sarcopenia in older British twins

BACKGROUND: Sarcopenia, characterised by an accelerated loss of skeletal muscle mass and function, is associated with negative outcomes. This study aimed to evaluate factors associated with skeletal muscle strength, mass and sarcopenia, particularly protein intake, and to assess whether shared twin...

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Autores principales: Ni Lochlainn, Mary, Bowyer, Ruth C E, Welch, Ailsa A, Whelan, Kevin, Steves, Claire J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10248216/
https://www.ncbi.nlm.nih.gov/pubmed/36800504
http://dx.doi.org/10.1093/ageing/afad018
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author Ni Lochlainn, Mary
Bowyer, Ruth C E
Welch, Ailsa A
Whelan, Kevin
Steves, Claire J
author_facet Ni Lochlainn, Mary
Bowyer, Ruth C E
Welch, Ailsa A
Whelan, Kevin
Steves, Claire J
author_sort Ni Lochlainn, Mary
collection PubMed
description BACKGROUND: Sarcopenia, characterised by an accelerated loss of skeletal muscle mass and function, is associated with negative outcomes. This study aimed to evaluate factors associated with skeletal muscle strength, mass and sarcopenia, particularly protein intake, and to assess whether shared twin characteristics are important. METHODS: This study utilised cross-sectional data from a study of community-dwelling twins aged ≥60 years. Multivariable logistic regression and between- and within-twin pair regression modelling were used. RESULTS: Participants (n = 3,302) were 89% female (n = 2,923), aged a mean of 72.1 (±7.3) years and composed of 858 (55%) monozygotic, 709 (45%) dizygotic twin pairs and 168 individual lone twins. Using optimal protein intake as the reference group (1.0–1.3 g/kg/day), there was no significant association between protein intake (neither high nor low) and low muscle strength, or between low protein intake and sarcopenia (odds ratio (OR) 0.7; 95% confidence interval (CI) 0.39–1.25; P = 0.229) in unadjusted models. High protein intake (>1.3 g/kg/day) was associated with low muscle mass (OR 1.76; 95% CI 1.39–2.24; P < 0.0001), while low protein intake was protective (OR 0.52; 95% CI 0.40–0.67; P < 0.0001). High protein intake was associated with sarcopenia (OR 2.04; 95% CI 1.21–3.44; P = 0.008), and this was robust to adjustment for demographic, anthropometric and dietary factors. The association between muscle strength and weight, body mass index, healthy eating index, protein intake and alpha diversity was not significantly influenced by shared twin factors, indicating greater amenability to interventions. CONCLUSIONS: High protein intake is associated with sarcopenia in a cohort of healthy older twins.
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spelling pubmed-102482162023-06-09 Higher dietary protein intake is associated with sarcopenia in older British twins Ni Lochlainn, Mary Bowyer, Ruth C E Welch, Ailsa A Whelan, Kevin Steves, Claire J Age Ageing Research Paper BACKGROUND: Sarcopenia, characterised by an accelerated loss of skeletal muscle mass and function, is associated with negative outcomes. This study aimed to evaluate factors associated with skeletal muscle strength, mass and sarcopenia, particularly protein intake, and to assess whether shared twin characteristics are important. METHODS: This study utilised cross-sectional data from a study of community-dwelling twins aged ≥60 years. Multivariable logistic regression and between- and within-twin pair regression modelling were used. RESULTS: Participants (n = 3,302) were 89% female (n = 2,923), aged a mean of 72.1 (±7.3) years and composed of 858 (55%) monozygotic, 709 (45%) dizygotic twin pairs and 168 individual lone twins. Using optimal protein intake as the reference group (1.0–1.3 g/kg/day), there was no significant association between protein intake (neither high nor low) and low muscle strength, or between low protein intake and sarcopenia (odds ratio (OR) 0.7; 95% confidence interval (CI) 0.39–1.25; P = 0.229) in unadjusted models. High protein intake (>1.3 g/kg/day) was associated with low muscle mass (OR 1.76; 95% CI 1.39–2.24; P < 0.0001), while low protein intake was protective (OR 0.52; 95% CI 0.40–0.67; P < 0.0001). High protein intake was associated with sarcopenia (OR 2.04; 95% CI 1.21–3.44; P = 0.008), and this was robust to adjustment for demographic, anthropometric and dietary factors. The association between muscle strength and weight, body mass index, healthy eating index, protein intake and alpha diversity was not significantly influenced by shared twin factors, indicating greater amenability to interventions. CONCLUSIONS: High protein intake is associated with sarcopenia in a cohort of healthy older twins. Oxford University Press 2023-02-14 /pmc/articles/PMC10248216/ /pubmed/36800504 http://dx.doi.org/10.1093/ageing/afad018 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the British Geriatrics Society. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Ni Lochlainn, Mary
Bowyer, Ruth C E
Welch, Ailsa A
Whelan, Kevin
Steves, Claire J
Higher dietary protein intake is associated with sarcopenia in older British twins
title Higher dietary protein intake is associated with sarcopenia in older British twins
title_full Higher dietary protein intake is associated with sarcopenia in older British twins
title_fullStr Higher dietary protein intake is associated with sarcopenia in older British twins
title_full_unstemmed Higher dietary protein intake is associated with sarcopenia in older British twins
title_short Higher dietary protein intake is associated with sarcopenia in older British twins
title_sort higher dietary protein intake is associated with sarcopenia in older british twins
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10248216/
https://www.ncbi.nlm.nih.gov/pubmed/36800504
http://dx.doi.org/10.1093/ageing/afad018
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