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Colocalization of cerebral iron with Amyloid beta in Mild Cognitive Impairment

Quantitative Susceptibility Mapping (QSM) MRI at 7 Tesla and 11-Carbon Pittsburgh-Compound-B PET were used for investigating the relationship between brain iron and Amyloid beta (Aβ) plaque-load in a context of increased risk for Alzheimer's disease (AD), as reflected by the Apolipoprotein E ε4...

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Autores principales: van Bergen, J. M. G., Li, X., Hua, J., Schreiner, S. J., Steininger, S. C., Quevenco, F. C., Wyss, M., Gietl, A. F., Treyer, V., Leh, S. E., Buck, F., Nitsch, R. M., Pruessmann, K. P., van Zijl, P. C. M., Hock, C., Unschuld, P. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5066274/
https://www.ncbi.nlm.nih.gov/pubmed/27748454
http://dx.doi.org/10.1038/srep35514
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author van Bergen, J. M. G.
Li, X.
Hua, J.
Schreiner, S. J.
Steininger, S. C.
Quevenco, F. C.
Wyss, M.
Gietl, A. F.
Treyer, V.
Leh, S. E.
Buck, F.
Nitsch, R. M.
Pruessmann, K. P.
van Zijl, P. C. M.
Hock, C.
Unschuld, P. G.
author_facet van Bergen, J. M. G.
Li, X.
Hua, J.
Schreiner, S. J.
Steininger, S. C.
Quevenco, F. C.
Wyss, M.
Gietl, A. F.
Treyer, V.
Leh, S. E.
Buck, F.
Nitsch, R. M.
Pruessmann, K. P.
van Zijl, P. C. M.
Hock, C.
Unschuld, P. G.
author_sort van Bergen, J. M. G.
collection PubMed
description Quantitative Susceptibility Mapping (QSM) MRI at 7 Tesla and 11-Carbon Pittsburgh-Compound-B PET were used for investigating the relationship between brain iron and Amyloid beta (Aβ) plaque-load in a context of increased risk for Alzheimer's disease (AD), as reflected by the Apolipoprotein E ε4 (APOE-e4) allele and mild cognitive impairment (MCI) in elderly subjects. Carriers of APOE-e4 with normal cognition had higher cortical Aβ-plaque-load than non-carriers. In MCI an association between APOE-e4 and higher Aβ-plaque-load was observable both for cortical and subcortical brain-regions. APOE-e4 and MCI was also associated with higher cortical iron. Moreover, cerebral iron significantly affected functional coupling, and was furthermore associated with increased Aβ-plaque-load (R(2)-adjusted = 0.80, p < 0.001) and APOE-e4 carrier status (p < 0.001) in MCI. This study confirms earlier reports on an association between increased brain iron-burden and risk for neurocognitive dysfunction due to AD, and indicates that disease-progression is conferred by spatial colocalization of brain iron deposits with Aβ-plaques.
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spelling pubmed-50662742016-10-26 Colocalization of cerebral iron with Amyloid beta in Mild Cognitive Impairment van Bergen, J. M. G. Li, X. Hua, J. Schreiner, S. J. Steininger, S. C. Quevenco, F. C. Wyss, M. Gietl, A. F. Treyer, V. Leh, S. E. Buck, F. Nitsch, R. M. Pruessmann, K. P. van Zijl, P. C. M. Hock, C. Unschuld, P. G. Sci Rep Article Quantitative Susceptibility Mapping (QSM) MRI at 7 Tesla and 11-Carbon Pittsburgh-Compound-B PET were used for investigating the relationship between brain iron and Amyloid beta (Aβ) plaque-load in a context of increased risk for Alzheimer's disease (AD), as reflected by the Apolipoprotein E ε4 (APOE-e4) allele and mild cognitive impairment (MCI) in elderly subjects. Carriers of APOE-e4 with normal cognition had higher cortical Aβ-plaque-load than non-carriers. In MCI an association between APOE-e4 and higher Aβ-plaque-load was observable both for cortical and subcortical brain-regions. APOE-e4 and MCI was also associated with higher cortical iron. Moreover, cerebral iron significantly affected functional coupling, and was furthermore associated with increased Aβ-plaque-load (R(2)-adjusted = 0.80, p < 0.001) and APOE-e4 carrier status (p < 0.001) in MCI. This study confirms earlier reports on an association between increased brain iron-burden and risk for neurocognitive dysfunction due to AD, and indicates that disease-progression is conferred by spatial colocalization of brain iron deposits with Aβ-plaques. Nature Publishing Group 2016-10-17 /pmc/articles/PMC5066274/ /pubmed/27748454 http://dx.doi.org/10.1038/srep35514 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
van Bergen, J. M. G.
Li, X.
Hua, J.
Schreiner, S. J.
Steininger, S. C.
Quevenco, F. C.
Wyss, M.
Gietl, A. F.
Treyer, V.
Leh, S. E.
Buck, F.
Nitsch, R. M.
Pruessmann, K. P.
van Zijl, P. C. M.
Hock, C.
Unschuld, P. G.
Colocalization of cerebral iron with Amyloid beta in Mild Cognitive Impairment
title Colocalization of cerebral iron with Amyloid beta in Mild Cognitive Impairment
title_full Colocalization of cerebral iron with Amyloid beta in Mild Cognitive Impairment
title_fullStr Colocalization of cerebral iron with Amyloid beta in Mild Cognitive Impairment
title_full_unstemmed Colocalization of cerebral iron with Amyloid beta in Mild Cognitive Impairment
title_short Colocalization of cerebral iron with Amyloid beta in Mild Cognitive Impairment
title_sort colocalization of cerebral iron with amyloid beta in mild cognitive impairment
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5066274/
https://www.ncbi.nlm.nih.gov/pubmed/27748454
http://dx.doi.org/10.1038/srep35514
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