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Cognitive plasticity in normal and pathological aging
The main goal of the present study is to examine to what extent age and cognitive impairment contribute to learning performance (cognitive plasticity, cognitive modifiability, or learning potential). To address this question, participants coming from four studies (Longitudinal Study of Active Aging,...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3267402/ https://www.ncbi.nlm.nih.gov/pubmed/22291469 http://dx.doi.org/10.2147/CIA.S27008 |
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author | Fernández-Ballesteros, Rocío Botella, Juan Zamarrón, María Dolores Molina, María Ángeles Cabras, Emilia Schettini, Rocío Tárraga, Lluis |
author_facet | Fernández-Ballesteros, Rocío Botella, Juan Zamarrón, María Dolores Molina, María Ángeles Cabras, Emilia Schettini, Rocío Tárraga, Lluis |
author_sort | Fernández-Ballesteros, Rocío |
collection | PubMed |
description | The main goal of the present study is to examine to what extent age and cognitive impairment contribute to learning performance (cognitive plasticity, cognitive modifiability, or learning potential). To address this question, participants coming from four studies (Longitudinal Study of Active Aging, age range, 55–75 years, N = 458; Longitudinal Study in the very old [90+], age range, 90–102, N = 188, and Cognitive Plasticity within the Course of Cognitive Impairment, 97 “Normal”, 57 mild cognitive impairment [MCI], and 98 Alzheimer’s disease [AD] patients) were examined through a measure of verbal learning (developed from Rey). The results show that all age, MCI, and AD groups learned across the five learning trials of that test, but significant differences were found due to age, pathology, and education. The effects of pathology (MCI and AD) can be expressed in a metric of “years of normal decline by age”; specifically, being MCI means suffering an impairment in performance that is equivalent to the decline of a normal individual during 15 years, whereas the impact of AD is equivalent to 22.7 years. Likewise, the improvement associated with about 5 years of education is equivalent to about 1 year less of normal aging. Also, the two pathological groups significantly differed from “normal” groups in the delayed trial of the test. The most dramatic difference is that between the “normal” group and the AD patients, which shows relatively poorer performance for the AD group in the delayed trial than in the first learning trial. The potential role of this unique effect for quick detection purposes of AD is assessed (in the 75–89 years age range, sensitivity and specificity equal 0.813 and 0.917, respectively). |
format | Online Article Text |
id | pubmed-3267402 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-32674022012-01-30 Cognitive plasticity in normal and pathological aging Fernández-Ballesteros, Rocío Botella, Juan Zamarrón, María Dolores Molina, María Ángeles Cabras, Emilia Schettini, Rocío Tárraga, Lluis Clin Interv Aging Original Research The main goal of the present study is to examine to what extent age and cognitive impairment contribute to learning performance (cognitive plasticity, cognitive modifiability, or learning potential). To address this question, participants coming from four studies (Longitudinal Study of Active Aging, age range, 55–75 years, N = 458; Longitudinal Study in the very old [90+], age range, 90–102, N = 188, and Cognitive Plasticity within the Course of Cognitive Impairment, 97 “Normal”, 57 mild cognitive impairment [MCI], and 98 Alzheimer’s disease [AD] patients) were examined through a measure of verbal learning (developed from Rey). The results show that all age, MCI, and AD groups learned across the five learning trials of that test, but significant differences were found due to age, pathology, and education. The effects of pathology (MCI and AD) can be expressed in a metric of “years of normal decline by age”; specifically, being MCI means suffering an impairment in performance that is equivalent to the decline of a normal individual during 15 years, whereas the impact of AD is equivalent to 22.7 years. Likewise, the improvement associated with about 5 years of education is equivalent to about 1 year less of normal aging. Also, the two pathological groups significantly differed from “normal” groups in the delayed trial of the test. The most dramatic difference is that between the “normal” group and the AD patients, which shows relatively poorer performance for the AD group in the delayed trial than in the first learning trial. The potential role of this unique effect for quick detection purposes of AD is assessed (in the 75–89 years age range, sensitivity and specificity equal 0.813 and 0.917, respectively). Dove Medical Press 2012 2012-01-04 /pmc/articles/PMC3267402/ /pubmed/22291469 http://dx.doi.org/10.2147/CIA.S27008 Text en © 2012 Fernández-Ballesteros et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Original Research Fernández-Ballesteros, Rocío Botella, Juan Zamarrón, María Dolores Molina, María Ángeles Cabras, Emilia Schettini, Rocío Tárraga, Lluis Cognitive plasticity in normal and pathological aging |
title | Cognitive plasticity in normal and pathological aging |
title_full | Cognitive plasticity in normal and pathological aging |
title_fullStr | Cognitive plasticity in normal and pathological aging |
title_full_unstemmed | Cognitive plasticity in normal and pathological aging |
title_short | Cognitive plasticity in normal and pathological aging |
title_sort | cognitive plasticity in normal and pathological aging |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3267402/ https://www.ncbi.nlm.nih.gov/pubmed/22291469 http://dx.doi.org/10.2147/CIA.S27008 |
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