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Development and validation of a frailty index in the Longitudinal Aging Study Amsterdam

BACKGROUND: Frailty is a state of increased vulnerability to adverse outcomes. The frailty index (FI), defined by the deficit accumulation approach, is a sensitive instrument to measure levels of frailty, and therefore important for longitudinal studies of aging. AIMS: To develop an FI in the Longit...

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Autores principales: Hoogendijk, Emiel O., Theou, Olga, Rockwood, Kenneth, Onwuteaka-Philipsen, Bregje D., Deeg, Dorly J. H., Huisman, Martijn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589777/
https://www.ncbi.nlm.nih.gov/pubmed/27896796
http://dx.doi.org/10.1007/s40520-016-0689-0
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author Hoogendijk, Emiel O.
Theou, Olga
Rockwood, Kenneth
Onwuteaka-Philipsen, Bregje D.
Deeg, Dorly J. H.
Huisman, Martijn
author_facet Hoogendijk, Emiel O.
Theou, Olga
Rockwood, Kenneth
Onwuteaka-Philipsen, Bregje D.
Deeg, Dorly J. H.
Huisman, Martijn
author_sort Hoogendijk, Emiel O.
collection PubMed
description BACKGROUND: Frailty is a state of increased vulnerability to adverse outcomes. The frailty index (FI), defined by the deficit accumulation approach, is a sensitive instrument to measure levels of frailty, and therefore important for longitudinal studies of aging. AIMS: To develop an FI in the Longitudinal Aging Study Amsterdam (LASA), and to examine the predictive validity of this FI for 19-year mortality. METHODS: LASA is an ongoing study among Dutch older adults, based on a nationally representative sample. A 32-item FI (LASA–FI) was developed at the second LASA measurement wave (1995–1996) among 2218 people aged 57–88 years. An FI score between 0 and 1 was calculated for each individual. The LASA–FI included health deficits from the physical, mental and cognitive domain and can be constructed for most LASA measurement waves. Associations with 19-year mortality were assessed using Kaplan–Meier curves and Cox proportional hazards models. RESULTS: The mean LASA–FI score was 0.19 (SD = 0.12), with a 99% upper limit of 0.53. Scores were higher in women than men (women = 0.20, SD = 0.13 vs. men = 0.17, SD = 0.11, p < 0.001). The average age-related increase in the log-transformed LASA–FI score was 3.5% per year. In a model adjusted for age and sex, the FI score was significantly associated with 19-year all-cause mortality (HR per 0.01 = 1.03, 95% CI 1.03–1.04, p < 0.001). DISCUSSION/CONCLUSIONS: The key characteristics of the LASA–FI were in line with findings from previous FI studies in population-based samples of older people. The LASA–FI score was associated with mortality and may serve as an internal and external reference value.
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spelling pubmed-55897772017-09-22 Development and validation of a frailty index in the Longitudinal Aging Study Amsterdam Hoogendijk, Emiel O. Theou, Olga Rockwood, Kenneth Onwuteaka-Philipsen, Bregje D. Deeg, Dorly J. H. Huisman, Martijn Aging Clin Exp Res Original Article BACKGROUND: Frailty is a state of increased vulnerability to adverse outcomes. The frailty index (FI), defined by the deficit accumulation approach, is a sensitive instrument to measure levels of frailty, and therefore important for longitudinal studies of aging. AIMS: To develop an FI in the Longitudinal Aging Study Amsterdam (LASA), and to examine the predictive validity of this FI for 19-year mortality. METHODS: LASA is an ongoing study among Dutch older adults, based on a nationally representative sample. A 32-item FI (LASA–FI) was developed at the second LASA measurement wave (1995–1996) among 2218 people aged 57–88 years. An FI score between 0 and 1 was calculated for each individual. The LASA–FI included health deficits from the physical, mental and cognitive domain and can be constructed for most LASA measurement waves. Associations with 19-year mortality were assessed using Kaplan–Meier curves and Cox proportional hazards models. RESULTS: The mean LASA–FI score was 0.19 (SD = 0.12), with a 99% upper limit of 0.53. Scores were higher in women than men (women = 0.20, SD = 0.13 vs. men = 0.17, SD = 0.11, p < 0.001). The average age-related increase in the log-transformed LASA–FI score was 3.5% per year. In a model adjusted for age and sex, the FI score was significantly associated with 19-year all-cause mortality (HR per 0.01 = 1.03, 95% CI 1.03–1.04, p < 0.001). DISCUSSION/CONCLUSIONS: The key characteristics of the LASA–FI were in line with findings from previous FI studies in population-based samples of older people. The LASA–FI score was associated with mortality and may serve as an internal and external reference value. Springer International Publishing 2016-11-28 2017 /pmc/articles/PMC5589777/ /pubmed/27896796 http://dx.doi.org/10.1007/s40520-016-0689-0 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Hoogendijk, Emiel O.
Theou, Olga
Rockwood, Kenneth
Onwuteaka-Philipsen, Bregje D.
Deeg, Dorly J. H.
Huisman, Martijn
Development and validation of a frailty index in the Longitudinal Aging Study Amsterdam
title Development and validation of a frailty index in the Longitudinal Aging Study Amsterdam
title_full Development and validation of a frailty index in the Longitudinal Aging Study Amsterdam
title_fullStr Development and validation of a frailty index in the Longitudinal Aging Study Amsterdam
title_full_unstemmed Development and validation of a frailty index in the Longitudinal Aging Study Amsterdam
title_short Development and validation of a frailty index in the Longitudinal Aging Study Amsterdam
title_sort development and validation of a frailty index in the longitudinal aging study amsterdam
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589777/
https://www.ncbi.nlm.nih.gov/pubmed/27896796
http://dx.doi.org/10.1007/s40520-016-0689-0
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