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Higher white matter hyperintensity lesion load is associated with reduced long-range functional connectivity.

Authors :
Quandt F
Fischer F
Schröder J
Heinze M
Lettow I
Frey BM
Kessner SS
Schulz M
Higgen FL
Cheng B
Gerloff C
Thomalla G
Source :
Brain communications [Brain Commun] 2020 Jul 20; Vol. 2 (2), pp. fcaa111. Date of Electronic Publication: 2020 Jul 20 (Print Publication: 2020).
Publication Year :
2020

Abstract

Cerebral small vessel disease is a common disease in the older population and is recognized as a major risk factor for cognitive decline and stroke. Small vessel disease is considered a global brain disease impacting the integrity of neuronal networks resulting in disturbances of structural and functional connectivity. A core feature of cerebral small vessel disease commonly present on neuroimaging is white matter hyperintensities. We studied high-resolution resting-state EEG, leveraging source reconstruction methods, in 35 participants with varying degree of white matter hyperintensities without clinically evident cognitive impairment in an observational study. In patients with increasing white matter lesion load, global theta power was increased independently of age. Whole-brain functional connectivity revealed a disrupted network confined to the alpha band in participants with higher white matter hyperintensities lesion load. The decrease of functional connectivity was evident in long-range connections, mostly originating or terminating in the frontal lobe. Cognitive testing revealed no global cognitive impairment; however, some participants revealed deficits of executive functions that were related to larger white matter hyperintensities lesion load. In summary, participants without clinical signs of mild cognitive impairment or dementia showed oscillatory changes that were significantly related to white matter lesion load. Hence, oscillatory neuronal network changes due to white matter lesions might act as biomarker prior to clinically relevant behavioural impairment.<br /> (© The Author(s) (2020). Published by Oxford University Press on behalf of the Guarantors of Brain.)

Details

Language :
English
ISSN :
2632-1297
Volume :
2
Issue :
2
Database :
MEDLINE
Journal :
Brain communications
Publication Type :
Academic Journal
Accession number :
33134915
Full Text :
https://doi.org/10.1093/braincomms/fcaa111