Literature DB >> 20739101

Association between white matter hyperintensities and executive decline in mild cognitive impairment is network dependent.

Heidi I L Jacobs1, Pieter Jelle Visser, Martin P J Van Boxtel, Giovanni B Frisoni, Magda Tsolaki, Panagiota Papapostolou, Flavio Nobili, Lars-Olof Wahlund, Lennart Minthon, Lutz Frölich, Harald Hampel, Hilkka Soininen, Laura van de Pol, Philip Scheltens, Frans E S Tan, Jelle Jolles, Frans R J Verhey.   

Abstract

White matter hyperintensities (WMH) in Mild Cognitive Impairment (MCI) have been associated with impaired executive functioning, although contradictory findings have been reported. The aim of this study was to examine whether WMH location influenced the relation between WMH and executive functioning in MCI participants (55-90 years) in the European multicenter memory-clinic-based DESCRIPA study, who underwent MRI scanning at baseline (N = 337). Linear mixed model analysis was performed to test the association between WMH damage in three networks (frontal-parietal, frontal-subcortical and frontal-parietal-subcortical network) and change in executive functioning over a 3-year period. WMH in the frontal-parietal and in the frontal-parietal-subcortical network were associated with decline in executive functioning. However, the frontal-subcortical network was not associated with change in executive functioning. Our results suggest that parietal WMH are a significant contributor to executive decline in MCI and that investigation of WMH in the cerebral networks supporting cognitive functions provide a new way to differentiate stable from cognitive declining MCI individuals.
Copyright © 2012 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20739101     DOI: 10.1016/j.neurobiolaging.2010.07.015

Source DB:  PubMed          Journal:  Neurobiol Aging        ISSN: 0197-4580            Impact factor:   4.673


  22 in total

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4.  Anatomical, functional and molecular biomarker applications of magnetic resonance neuroimaging.

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8.  White matter hypoperfusion and damage in dementia: post-mortem assessment.

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10.  Associations between T1 white matter lesion volume and regional white matter microstructure in aging.

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