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Weight loss in the healthy elderly might be a non-cognitive sign of preclinical Alzheimer's disease

Weight loss has been proposed as a sign of pre-clinical Alzheimer Disease (AD). To test this hypothesis, we have evaluated the association between longitudinal changes in weight trajectories, cognitive performance, AD biomarker profiles and brain structure in 363 healthy controls from the Alzheimer´...

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Autores principales: Jimenez, Amanda, Pegueroles, Jordi, Carmona-Iragui, María, Vilaplana, Eduard, Montal, Victor, Alcolea, Daniel, Videla, Laura, Illán-Gala, Ignacio, Pané, Adriana, Casajoana, Anna, Belbin, Olivia, Clarimón, Jordi, Moizé, Violeta, Vidal, Josep, Lleó, Alberto, Fortea, Juan, Blesa, Rafael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5739594/
https://www.ncbi.nlm.nih.gov/pubmed/29285207
http://dx.doi.org/10.18632/oncotarget.22218
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author Jimenez, Amanda
Pegueroles, Jordi
Carmona-Iragui, María
Vilaplana, Eduard
Montal, Victor
Alcolea, Daniel
Videla, Laura
Illán-Gala, Ignacio
Pané, Adriana
Casajoana, Anna
Belbin, Olivia
Clarimón, Jordi
Moizé, Violeta
Vidal, Josep
Lleó, Alberto
Fortea, Juan
Blesa, Rafael
author_facet Jimenez, Amanda
Pegueroles, Jordi
Carmona-Iragui, María
Vilaplana, Eduard
Montal, Victor
Alcolea, Daniel
Videla, Laura
Illán-Gala, Ignacio
Pané, Adriana
Casajoana, Anna
Belbin, Olivia
Clarimón, Jordi
Moizé, Violeta
Vidal, Josep
Lleó, Alberto
Fortea, Juan
Blesa, Rafael
author_sort Jimenez, Amanda
collection PubMed
description Weight loss has been proposed as a sign of pre-clinical Alzheimer Disease (AD). To test this hypothesis, we have evaluated the association between longitudinal changes in weight trajectories, cognitive performance, AD biomarker profiles and brain structure in 363 healthy controls from the Alzheimer´s Disease Neuroimaging Initiative (mean follow-up 50.5±30.5 months). Subjects were classified according to body weight trajectory into a weight loss group (WLG; relative weight loss ≥ 5%) and a non-weight loss group (non-WLG; relative weight loss < 5%). Linear mixed effects models were used to estimate the effect of body weight changes on ADAS-Cognitive score across time. Baseline CSF tau/AΔ(42) ratio and AV45 PET uptake were compared between WLG and non-WLG by analysis of covariance. Atrophy maps were compared between groups at baseline and longitudinally at a 2-year follow-up using Freesurfer. WLG showed increased baseline levels of cerebrospinal fluid tau/AΔ(42) ratio, increased PET amyloid uptake and diminished cortical thickness at baseline. WLG also showed faster cognitive decline and faster longitudinal atrophy. Our data support weight loss as a non-cognitive manifestation of pre-clinical AD.
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spelling pubmed-57395942017-12-28 Weight loss in the healthy elderly might be a non-cognitive sign of preclinical Alzheimer's disease Jimenez, Amanda Pegueroles, Jordi Carmona-Iragui, María Vilaplana, Eduard Montal, Victor Alcolea, Daniel Videla, Laura Illán-Gala, Ignacio Pané, Adriana Casajoana, Anna Belbin, Olivia Clarimón, Jordi Moizé, Violeta Vidal, Josep Lleó, Alberto Fortea, Juan Blesa, Rafael Oncotarget Research Paper: Gerotarget (Focus on Aging) Weight loss has been proposed as a sign of pre-clinical Alzheimer Disease (AD). To test this hypothesis, we have evaluated the association between longitudinal changes in weight trajectories, cognitive performance, AD biomarker profiles and brain structure in 363 healthy controls from the Alzheimer´s Disease Neuroimaging Initiative (mean follow-up 50.5±30.5 months). Subjects were classified according to body weight trajectory into a weight loss group (WLG; relative weight loss ≥ 5%) and a non-weight loss group (non-WLG; relative weight loss < 5%). Linear mixed effects models were used to estimate the effect of body weight changes on ADAS-Cognitive score across time. Baseline CSF tau/AΔ(42) ratio and AV45 PET uptake were compared between WLG and non-WLG by analysis of covariance. Atrophy maps were compared between groups at baseline and longitudinally at a 2-year follow-up using Freesurfer. WLG showed increased baseline levels of cerebrospinal fluid tau/AΔ(42) ratio, increased PET amyloid uptake and diminished cortical thickness at baseline. WLG also showed faster cognitive decline and faster longitudinal atrophy. Our data support weight loss as a non-cognitive manifestation of pre-clinical AD. Impact Journals LLC 2017-10-31 /pmc/articles/PMC5739594/ /pubmed/29285207 http://dx.doi.org/10.18632/oncotarget.22218 Text en Copyright: © 2017 Jimenez et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper: Gerotarget (Focus on Aging)
Jimenez, Amanda
Pegueroles, Jordi
Carmona-Iragui, María
Vilaplana, Eduard
Montal, Victor
Alcolea, Daniel
Videla, Laura
Illán-Gala, Ignacio
Pané, Adriana
Casajoana, Anna
Belbin, Olivia
Clarimón, Jordi
Moizé, Violeta
Vidal, Josep
Lleó, Alberto
Fortea, Juan
Blesa, Rafael
Weight loss in the healthy elderly might be a non-cognitive sign of preclinical Alzheimer's disease
title Weight loss in the healthy elderly might be a non-cognitive sign of preclinical Alzheimer's disease
title_full Weight loss in the healthy elderly might be a non-cognitive sign of preclinical Alzheimer's disease
title_fullStr Weight loss in the healthy elderly might be a non-cognitive sign of preclinical Alzheimer's disease
title_full_unstemmed Weight loss in the healthy elderly might be a non-cognitive sign of preclinical Alzheimer's disease
title_short Weight loss in the healthy elderly might be a non-cognitive sign of preclinical Alzheimer's disease
title_sort weight loss in the healthy elderly might be a non-cognitive sign of preclinical alzheimer's disease
topic Research Paper: Gerotarget (Focus on Aging)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5739594/
https://www.ncbi.nlm.nih.gov/pubmed/29285207
http://dx.doi.org/10.18632/oncotarget.22218
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