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Frailty in a racially and socioeconomically diverse sample of middle-aged Americans in Baltimore
Frailty is a risk factor for disability and mortality, and is more prevalent among African American (AA) elderly than whites. We examine frailty in middle-aged racially and economically diverse adults, and investigate how race, poverty and frailty are associated with mortality. Data were from 2541 p...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5892911/ https://www.ncbi.nlm.nih.gov/pubmed/29634767 http://dx.doi.org/10.1371/journal.pone.0195637 |
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author | Griffin, Felicia R. Mode, Nicolle A. Ejiogu, Ngozi Zonderman, Alan B. Evans, Michele K. |
author_facet | Griffin, Felicia R. Mode, Nicolle A. Ejiogu, Ngozi Zonderman, Alan B. Evans, Michele K. |
author_sort | Griffin, Felicia R. |
collection | PubMed |
description | Frailty is a risk factor for disability and mortality, and is more prevalent among African American (AA) elderly than whites. We examine frailty in middle-aged racially and economically diverse adults, and investigate how race, poverty and frailty are associated with mortality. Data were from 2541 participants in the Healthy Aging in Neighborhoods of Diversity across the Life Span study in Baltimore, Maryland; 35–64 years old at initial assessment (56% women; 58% AA). Frailty was assessed using a modified FRAIL scale of fatigue, resistance, ambulation, illness and weight loss, and compared with difficulties in physical functioning and daily activities. Frailty prevalence was calculated across race and age groups, and associations with survival were assessed by Cox Regression. 278 participants were frail (11%); 924 pre-frail (36%); 1339 not frail (53%). For those aged 45–54, a higher proportion of whites (13%) than AAs (8%) were frail; while the proportions were similar for those 55–64 (14%,16%). Frailty was associated with overall survival with an average follow-up of 6.6 years, independent of race, sex and poverty status (HR = 2.30; 95%CI 1.67–3.18). In this sample of economically and racially diverse older adults, the known association of frailty prevalence and age differed across race with whites having higher prevalence at younger ages. Frailty was associated with survival beyond the risk factors of race and poverty status in this middle-aged group. Early recognition of frailty at these younger ages may provide an effective method for preventing or delaying disabilities. |
format | Online Article Text |
id | pubmed-5892911 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-58929112018-04-20 Frailty in a racially and socioeconomically diverse sample of middle-aged Americans in Baltimore Griffin, Felicia R. Mode, Nicolle A. Ejiogu, Ngozi Zonderman, Alan B. Evans, Michele K. PLoS One Research Article Frailty is a risk factor for disability and mortality, and is more prevalent among African American (AA) elderly than whites. We examine frailty in middle-aged racially and economically diverse adults, and investigate how race, poverty and frailty are associated with mortality. Data were from 2541 participants in the Healthy Aging in Neighborhoods of Diversity across the Life Span study in Baltimore, Maryland; 35–64 years old at initial assessment (56% women; 58% AA). Frailty was assessed using a modified FRAIL scale of fatigue, resistance, ambulation, illness and weight loss, and compared with difficulties in physical functioning and daily activities. Frailty prevalence was calculated across race and age groups, and associations with survival were assessed by Cox Regression. 278 participants were frail (11%); 924 pre-frail (36%); 1339 not frail (53%). For those aged 45–54, a higher proportion of whites (13%) than AAs (8%) were frail; while the proportions were similar for those 55–64 (14%,16%). Frailty was associated with overall survival with an average follow-up of 6.6 years, independent of race, sex and poverty status (HR = 2.30; 95%CI 1.67–3.18). In this sample of economically and racially diverse older adults, the known association of frailty prevalence and age differed across race with whites having higher prevalence at younger ages. Frailty was associated with survival beyond the risk factors of race and poverty status in this middle-aged group. Early recognition of frailty at these younger ages may provide an effective method for preventing or delaying disabilities. Public Library of Science 2018-04-10 /pmc/articles/PMC5892911/ /pubmed/29634767 http://dx.doi.org/10.1371/journal.pone.0195637 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Griffin, Felicia R. Mode, Nicolle A. Ejiogu, Ngozi Zonderman, Alan B. Evans, Michele K. Frailty in a racially and socioeconomically diverse sample of middle-aged Americans in Baltimore |
title | Frailty in a racially and socioeconomically diverse sample of middle-aged Americans in Baltimore |
title_full | Frailty in a racially and socioeconomically diverse sample of middle-aged Americans in Baltimore |
title_fullStr | Frailty in a racially and socioeconomically diverse sample of middle-aged Americans in Baltimore |
title_full_unstemmed | Frailty in a racially and socioeconomically diverse sample of middle-aged Americans in Baltimore |
title_short | Frailty in a racially and socioeconomically diverse sample of middle-aged Americans in Baltimore |
title_sort | frailty in a racially and socioeconomically diverse sample of middle-aged americans in baltimore |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5892911/ https://www.ncbi.nlm.nih.gov/pubmed/29634767 http://dx.doi.org/10.1371/journal.pone.0195637 |
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