2018
DOI: 10.1093/brain/awy180
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Neurophysiological signatures of Alzheimer’s disease and frontotemporal lobar degeneration: pathology versus phenotype

Abstract: Sami et al. identify characteristic neurophysiological signatures of five neurodegenerative diseases, including two variants of Alzheimer’s disease and three forms of frontotemporal lobar degeneration. Disorders that share a common underlying pathology have a similar spectral signature of altered connectivity, regardless of phenotype.

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Cited by 63 publications
(61 citation statements)
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“…Artifact-related components were removed. MEG data were segmented into 4-second epochs and filtered using a 2000th order FIR band-pass filter with a Hanning window into five bands (with 2 seconds of real data padding added either side): for source analysis: broad band (2-45 Hz), and for connectivity analysis: theta (4-8 Hz), alpha (8-12 Hz), beta (12)(13)(14)(15)(16)(17)(18)(19)(20)(21)(22)(23)(24)(25)(26)(27)(28)(29)(30), and gamma (30)(31)(32)(33)(34)(35)(36)(37)(38)(39)(40)(41)(42)(43)(44)(45). The data were coregistered to the T1-weighted MRI and the forward model calculated using a realistic single shell head [11].…”
Section: Analysis 3: Source-level Power Analyses and Functional Connementioning
confidence: 99%
“…Artifact-related components were removed. MEG data were segmented into 4-second epochs and filtered using a 2000th order FIR band-pass filter with a Hanning window into five bands (with 2 seconds of real data padding added either side): for source analysis: broad band (2-45 Hz), and for connectivity analysis: theta (4-8 Hz), alpha (8-12 Hz), beta (12)(13)(14)(15)(16)(17)(18)(19)(20)(21)(22)(23)(24)(25)(26)(27)(28)(29)(30), and gamma (30)(31)(32)(33)(34)(35)(36)(37)(38)(39)(40)(41)(42)(43)(44)(45). The data were coregistered to the T1-weighted MRI and the forward model calculated using a realistic single shell head [11].…”
Section: Analysis 3: Source-level Power Analyses and Functional Connementioning
confidence: 99%
“…MEG has only been deployed recently to investigate PPA (e.g., Kielar et al, 2018), but has already shown its potential as a tool to study the neurophysiological signatures of network-level alterations due to neurodegenerative disorders. It can be instrumental in identifying syndromespecific changes in the spectral properties of oscillatory responses (Ranasinghe et al, 2017;Sami et al, 2018). As suggested by task-free fMRI evidence, these functional alterations might precede structural ones and may be key for early diagnosis (Bonakdarpour et al, 2017).…”
Section: The Latency Of the Dorsal Activation Indicates Slow Serial mentioning
confidence: 99%
“…, to capture movement-intentions (Wolpaw et al, 1991;Lotte et al, 2007;Tangermann et al, 2008). For biomarkers applications, the focus is on predicting medical diagnosis and other clinical endpoints Sami et al, 2018;Mazaheri et al, 2018).…”
Section: Introductionmentioning
confidence: 99%