TY - JOUR
T1 - Alpha desynchronization during Stroop test unmasks cognitively healthy individuals with abnormal CSF Amyloid/Tau
AU - Arakaki, Xianghong
AU - Hung, Shao Min
AU - Rochart, Roger
AU - Fonteh, Alfred N.
AU - Harrington, Michael G.
N1 - Funding Information:
We thank the study participants for their contributions. Betty Chung and David Buennagel assisted with participant recruitment. Dr. Anne Nolty and faculty-supervised graduate students of Fuller psychology department performed psychometry testing. Dr. Helena Chui and Dr. Kloner helped with clinical conference for participant classification. Dr. Kloner, Dr. Kleinman, and Dr. Rebecca J Arechavala edited the manuscript. Dr. Quanying Liu helped with the estimated Innotest amyloid and tau conversions. Some data relied upon in this study was derived from research performed at HMRI by Dr. Michael G. Harrington. This work was supported by the National Institutes of Aging [grant number R56AG063857 , R01AG063857 ] and L. K. Whittier Foundation.
Publisher Copyright:
© 2021 Elsevier Inc.
PY - 2022/4
Y1 - 2022/4
N2 - Synaptic dysfunctions precede cognitive decline in Alzheimer's disease by decades, affect executive functions, and can be detected by quantitative electroencephalography (qEEG). We used quantitative electroencephalography combined with Stroop testing to identify changes of inhibitory controls in cognitively healthy individuals with an abnormal versus normal ratio of cerebrospinal fluid (CSF) amyloid/total-tau. We studied two groups of participants (60–94 years) with either normal (CH-NAT or controls, n = 20) or abnormal (CH-PAT, n = 21) CSF amyloid/tau ratio. We compared: alpha event-related desynchronization (ERD), alpha spectral entropy (SE), and their relationships with estimated cognitive reserve. CH-PATs had more negative occipital alpha ERD, and higher frontal and occipital alpha SE during low load congruent trials, indicating hyperactivity. CH-PATs demonstrated fewer frontal SE changes with higher load, incongruent Stroop testing. Correlations of alpha ERD with estimated cognitive reserve were significant in CH-PATs but not in CH-NATs. These results suggested compensatory hyperactivity in CH-PATs compared to CH-NATs. We did not find differences in alpha ERD comparisons with individual CSF amyloid(A), p-tau(T), total-tau(N) biomarkers.
AB - Synaptic dysfunctions precede cognitive decline in Alzheimer's disease by decades, affect executive functions, and can be detected by quantitative electroencephalography (qEEG). We used quantitative electroencephalography combined with Stroop testing to identify changes of inhibitory controls in cognitively healthy individuals with an abnormal versus normal ratio of cerebrospinal fluid (CSF) amyloid/total-tau. We studied two groups of participants (60–94 years) with either normal (CH-NAT or controls, n = 20) or abnormal (CH-PAT, n = 21) CSF amyloid/tau ratio. We compared: alpha event-related desynchronization (ERD), alpha spectral entropy (SE), and their relationships with estimated cognitive reserve. CH-PATs had more negative occipital alpha ERD, and higher frontal and occipital alpha SE during low load congruent trials, indicating hyperactivity. CH-PATs demonstrated fewer frontal SE changes with higher load, incongruent Stroop testing. Correlations of alpha ERD with estimated cognitive reserve were significant in CH-PATs but not in CH-NATs. These results suggested compensatory hyperactivity in CH-PATs compared to CH-NATs. We did not find differences in alpha ERD comparisons with individual CSF amyloid(A), p-tau(T), total-tau(N) biomarkers.
KW - CH-NATs
KW - CH-PATs
KW - Stroop
KW - alpha event-related desynchronization
KW - electroencephalography
KW - spectral entropy
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U2 - 10.1016/j.neurobiolaging.2021.11.009
DO - 10.1016/j.neurobiolaging.2021.11.009
M3 - Article
C2 - 35066324
AN - SCOPUS:85123067257
SN - 0197-4580
VL - 112
SP - 87
EP - 101
JO - Neurobiology of Aging
JF - Neurobiology of Aging
ER -