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Intake of Flavonoids and Odds of Frailty Onset in Adults in the Framingham Offspring Cohort
Polyphenols (antioxidants derived from plant-foods) could play a role in inhibition of oxidative stress and frailty reduction, yet data on the polyphenol subclass of dietary flavonoids is limited. This study sought to determine the association between dietary flavonoids and frailty onset in middle-a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8969543/ http://dx.doi.org/10.1093/geroni/igab046.3618 |
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author | Nguyen, Thuy Nga Millar, Courtney Kiel, Douglas Hannan, Marian Sahni, Shivani |
author_facet | Nguyen, Thuy Nga Millar, Courtney Kiel, Douglas Hannan, Marian Sahni, Shivani |
author_sort | Nguyen, Thuy Nga |
collection | PubMed |
description | Polyphenols (antioxidants derived from plant-foods) could play a role in inhibition of oxidative stress and frailty reduction, yet data on the polyphenol subclass of dietary flavonoids is limited. This study sought to determine the association between dietary flavonoids and frailty onset in middle-aged and older adults. This prospective cohort study included non-frail individuals from the Framingham Offspring Cohort (FOC) with total flavonoid intake (mg/day; defined as sum flavonols, flavan-3-ols, flavonones, flavones, and anthocyanins via Harvard Food Frequency Questionnaire), frailty (via Fried phenotype), and covariate information measured at baseline (1998-2001). Follow-up frailty was evaluated in 2011-2014. Logistic regression estimated odds ratio (OR) and 95% confidence intervals (95% CI) adjusting for relevant confounders. Participants (n=1,701; 55.5% female) had a mean age of 58.4 years (SD ± 8.3). Mean flavonoid intake was 309 mg/d (SD ± 266). After 12.4 years (SD ± 0.8), 224 (13.2%) individuals exhibited frailty. In age and sex adjusted models, every 50 mg/day of higher total flavonoid intake was associated with 3% reduced odds of frailty [OR (95%CI): 0.97 (0.94-1.00), p-value: 0.05). Further adjustment for smoking, energy and protein intake, and disease indicators did not appreciably change the association, and associations became non-significant (p-value=0.12). Thus, there was no association between flavonoid intake and odds of frailty onset in adults in the FOC. This could be due to participants' higher intake of flavonoids compared to average intake of ~200 mg/d in Americans. |
format | Online Article Text |
id | pubmed-8969543 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-89695432022-04-01 Intake of Flavonoids and Odds of Frailty Onset in Adults in the Framingham Offspring Cohort Nguyen, Thuy Nga Millar, Courtney Kiel, Douglas Hannan, Marian Sahni, Shivani Innov Aging Abstracts Polyphenols (antioxidants derived from plant-foods) could play a role in inhibition of oxidative stress and frailty reduction, yet data on the polyphenol subclass of dietary flavonoids is limited. This study sought to determine the association between dietary flavonoids and frailty onset in middle-aged and older adults. This prospective cohort study included non-frail individuals from the Framingham Offspring Cohort (FOC) with total flavonoid intake (mg/day; defined as sum flavonols, flavan-3-ols, flavonones, flavones, and anthocyanins via Harvard Food Frequency Questionnaire), frailty (via Fried phenotype), and covariate information measured at baseline (1998-2001). Follow-up frailty was evaluated in 2011-2014. Logistic regression estimated odds ratio (OR) and 95% confidence intervals (95% CI) adjusting for relevant confounders. Participants (n=1,701; 55.5% female) had a mean age of 58.4 years (SD ± 8.3). Mean flavonoid intake was 309 mg/d (SD ± 266). After 12.4 years (SD ± 0.8), 224 (13.2%) individuals exhibited frailty. In age and sex adjusted models, every 50 mg/day of higher total flavonoid intake was associated with 3% reduced odds of frailty [OR (95%CI): 0.97 (0.94-1.00), p-value: 0.05). Further adjustment for smoking, energy and protein intake, and disease indicators did not appreciably change the association, and associations became non-significant (p-value=0.12). Thus, there was no association between flavonoid intake and odds of frailty onset in adults in the FOC. This could be due to participants' higher intake of flavonoids compared to average intake of ~200 mg/d in Americans. Oxford University Press 2021-12-17 /pmc/articles/PMC8969543/ http://dx.doi.org/10.1093/geroni/igab046.3618 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of The Gerontological Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (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 | Abstracts Nguyen, Thuy Nga Millar, Courtney Kiel, Douglas Hannan, Marian Sahni, Shivani Intake of Flavonoids and Odds of Frailty Onset in Adults in the Framingham Offspring Cohort |
title | Intake of Flavonoids and Odds of Frailty Onset in Adults in the Framingham Offspring Cohort |
title_full | Intake of Flavonoids and Odds of Frailty Onset in Adults in the Framingham Offspring Cohort |
title_fullStr | Intake of Flavonoids and Odds of Frailty Onset in Adults in the Framingham Offspring Cohort |
title_full_unstemmed | Intake of Flavonoids and Odds of Frailty Onset in Adults in the Framingham Offspring Cohort |
title_short | Intake of Flavonoids and Odds of Frailty Onset in Adults in the Framingham Offspring Cohort |
title_sort | intake of flavonoids and odds of frailty onset in adults in the framingham offspring cohort |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8969543/ http://dx.doi.org/10.1093/geroni/igab046.3618 |
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