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Beyond Frequency Bands: Complementary-Ensemble-Empirical-Mode-Decomposition-Enhanced Microstate Sequence Non-Randomness Analysis for Aiding Diagnosis and Cognitive Prediction of Dementia
Exploring the spatiotemporal dynamic patterns of multi-channel electroencephalography (EEG) is crucial for interpreting dementia and related cognitive decline. Spatiotemporal patterns of EEG can be described through microstate analysis, which provides a discrete approximation of the continuous elect...
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description | Exploring the spatiotemporal dynamic patterns of multi-channel electroencephalography (EEG) is crucial for interpreting dementia and related cognitive decline. Spatiotemporal patterns of EEG can be described through microstate analysis, which provides a discrete approximation of the continuous electric field patterns generated by the brain cortex. Here, we propose a novel microstate spatiotemporal dynamic indicator, termed the microstate sequence non-randomness index (MSNRI). The essence of the method lies in initially generating a sequence of microstate transition patterns through state space compression of EEG data using microstate analysis. Following this, we assess the non-randomness of these microstate patterns using information-based similarity analysis. The results suggest that this MSNRI metric is a potential marker for distinguishing between health control (HC) and frontotemporal dementia (FTD) (HC vs. FTD: 6.958 vs. 5.756,
< 0.01), as well as between HC and populations with Alzheimer's disease (AD) (HC vs. AD: 6.958 vs. 5.462,
< 0.001). Healthy individuals exhibit more complex macroscopic structures and non-random spatiotemporal patterns of microstates, whereas dementia disorders lead to more random spatiotemporal patterns. Additionally, we extend the proposed method by integrating the Complementary Ensemble Empirical Mode Decomposition (CEEMD) method to explore spatiotemporal dynamic patterns of microstates at specific frequency scales. Moreover, we assessed the effectiveness of this innovative method in predicting cognitive scores. The results demonstrate that the incorporation of CEEMD-enhanced microstate dynamic indicators significantly improved the prediction accuracy of Mini-Mental State Examination (MMSE) scores (R
= 0.940). The CEEMD-enhanced MSNRI method not only aids in the exploration of large-scale neural changes in populations with dementia but also offers a robust tool for characterizing the dynamics of EEG microstate transitions and their impact on cognitive function. |
doi_str_mv | 10.3390/brainsci14050487 |
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< 0.01), as well as between HC and populations with Alzheimer's disease (AD) (HC vs. AD: 6.958 vs. 5.462,
< 0.001). Healthy individuals exhibit more complex macroscopic structures and non-random spatiotemporal patterns of microstates, whereas dementia disorders lead to more random spatiotemporal patterns. Additionally, we extend the proposed method by integrating the Complementary Ensemble Empirical Mode Decomposition (CEEMD) method to explore spatiotemporal dynamic patterns of microstates at specific frequency scales. Moreover, we assessed the effectiveness of this innovative method in predicting cognitive scores. The results demonstrate that the incorporation of CEEMD-enhanced microstate dynamic indicators significantly improved the prediction accuracy of Mini-Mental State Examination (MMSE) scores (R
= 0.940). The CEEMD-enhanced MSNRI method not only aids in the exploration of large-scale neural changes in populations with dementia but also offers a robust tool for characterizing the dynamics of EEG microstate transitions and their impact on cognitive function.</description><identifier>ISSN: 2076-3425</identifier><identifier>EISSN: 2076-3425</identifier><identifier>DOI: 10.3390/brainsci14050487</identifier><identifier>PMID: 38790465</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Advertising executives ; Alzheimer's disease ; Biomarkers ; Brain research ; Cognitive ability ; Datasets ; Dementia ; Dementia disorders ; Disease ; EEG ; electroencephalogram ; Electroencephalography ; Frontotemporal dementia ; information-based similarity ; Medical research ; Medicine, Experimental ; Methods ; microstate transitions ; Neurodegenerative diseases ; non-randomness ; Recording sessions</subject><ispartof>Brain sciences, 2024-05, Vol.14 (5), p.487</ispartof><rights>COPYRIGHT 2024 MDPI AG</rights><rights>2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c385t-122e538fb455453c6395f21fc17b428c0b9cdeaa4c482ba56ea4e8d95c7928a93</cites><orcidid>0000-0003-1887-8631 ; 0000-0003-3666-9833</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3059406791/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3059406791?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25751,27922,27923,37010,37011,38514,43893,44588,74182,74896</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38790465$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wan, Wang</creatorcontrib><creatorcontrib>Gu, Zhongze</creatorcontrib><creatorcontrib>Peng, Chung-Kang</creatorcontrib><creatorcontrib>Cui, Xingran</creatorcontrib><title>Beyond Frequency Bands: Complementary-Ensemble-Empirical-Mode-Decomposition-Enhanced Microstate Sequence Non-Randomness Analysis for Aiding Diagnosis and Cognitive Prediction of Dementia</title><title>Brain sciences</title><addtitle>Brain Sci</addtitle><description>Exploring the spatiotemporal dynamic patterns of multi-channel electroencephalography (EEG) is crucial for interpreting dementia and related cognitive decline. Spatiotemporal patterns of EEG can be described through microstate analysis, which provides a discrete approximation of the continuous electric field patterns generated by the brain cortex. Here, we propose a novel microstate spatiotemporal dynamic indicator, termed the microstate sequence non-randomness index (MSNRI). The essence of the method lies in initially generating a sequence of microstate transition patterns through state space compression of EEG data using microstate analysis. Following this, we assess the non-randomness of these microstate patterns using information-based similarity analysis. The results suggest that this MSNRI metric is a potential marker for distinguishing between health control (HC) and frontotemporal dementia (FTD) (HC vs. FTD: 6.958 vs. 5.756,
< 0.01), as well as between HC and populations with Alzheimer's disease (AD) (HC vs. AD: 6.958 vs. 5.462,
< 0.001). Healthy individuals exhibit more complex macroscopic structures and non-random spatiotemporal patterns of microstates, whereas dementia disorders lead to more random spatiotemporal patterns. Additionally, we extend the proposed method by integrating the Complementary Ensemble Empirical Mode Decomposition (CEEMD) method to explore spatiotemporal dynamic patterns of microstates at specific frequency scales. Moreover, we assessed the effectiveness of this innovative method in predicting cognitive scores. The results demonstrate that the incorporation of CEEMD-enhanced microstate dynamic indicators significantly improved the prediction accuracy of Mini-Mental State Examination (MMSE) scores (R
= 0.940). The CEEMD-enhanced MSNRI method not only aids in the exploration of large-scale neural changes in populations with dementia but also offers a robust tool for characterizing the dynamics of EEG microstate transitions and their impact on cognitive function.</description><subject>Advertising executives</subject><subject>Alzheimer's disease</subject><subject>Biomarkers</subject><subject>Brain research</subject><subject>Cognitive ability</subject><subject>Datasets</subject><subject>Dementia</subject><subject>Dementia disorders</subject><subject>Disease</subject><subject>EEG</subject><subject>electroencephalogram</subject><subject>Electroencephalography</subject><subject>Frontotemporal dementia</subject><subject>information-based similarity</subject><subject>Medical research</subject><subject>Medicine, Experimental</subject><subject>Methods</subject><subject>microstate transitions</subject><subject>Neurodegenerative diseases</subject><subject>non-randomness</subject><subject>Recording sessions</subject><issn>2076-3425</issn><issn>2076-3425</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>COVID</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkk1v1DAQQCMEolXpnROyxIVLihPbccxtu7uFSi0gPs7RxB4vrhJ7sbNI-9f4dTjdUqAiPsQavXkej6conlf0jDFFX_cRnE_aVZwKylv5qDiuqWxKxmvx-K_9UXGa0g3NX0spE_RpccRaqShvxHHx8xz3wRtyEfH7Dr3ek3PwJr0hyzBuBxzRTxD35donHPsBy_W4ddFpGMrrYLBcoc5cSG5ywWfqG3iNhlw7HUOaYELy-eBF8j4Dn7I7jB5TIgsPwz65RGyIZOGM8xuycrDxYQ5mLlew8dn7A8nHiMbp-QgSLFndVuXgWfHEwpDw9O5_Uny9WH9ZviuvPry9XC6uSs1aMZVVXaNgre25EFww3TAlbF1ZXcme162mvdIGAbjmbd2DaBA4tkYJLVXdgmInxeXBawLcdNvoxtyRLoDrbgMhbjqIk9MDdj0DphGlbWS2gQBJKyZUnb0GrYbsenVwbWPIfUlTN7qkcRjAY9iljtGGMsl5RTP68gF6E3Yxd22mhOK0kar6Q20gn--8DVMEPUu7hVSCybZpZabO_kPlZXB0Oni0Lsf_SaCHhPkdU0R7f--KdvP0dQ-nL6e8uKt3149o7hN-zxr7BaK32Rk</recordid><startdate>20240501</startdate><enddate>20240501</enddate><creator>Wan, Wang</creator><creator>Gu, Zhongze</creator><creator>Peng, Chung-Kang</creator><creator>Cui, Xingran</creator><general>MDPI AG</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>COVID</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-1887-8631</orcidid><orcidid>https://orcid.org/0000-0003-3666-9833</orcidid></search><sort><creationdate>20240501</creationdate><title>Beyond Frequency Bands: Complementary-Ensemble-Empirical-Mode-Decomposition-Enhanced Microstate Sequence Non-Randomness Analysis for Aiding Diagnosis and Cognitive Prediction of Dementia</title><author>Wan, Wang ; 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Spatiotemporal patterns of EEG can be described through microstate analysis, which provides a discrete approximation of the continuous electric field patterns generated by the brain cortex. Here, we propose a novel microstate spatiotemporal dynamic indicator, termed the microstate sequence non-randomness index (MSNRI). The essence of the method lies in initially generating a sequence of microstate transition patterns through state space compression of EEG data using microstate analysis. Following this, we assess the non-randomness of these microstate patterns using information-based similarity analysis. The results suggest that this MSNRI metric is a potential marker for distinguishing between health control (HC) and frontotemporal dementia (FTD) (HC vs. FTD: 6.958 vs. 5.756,
< 0.01), as well as between HC and populations with Alzheimer's disease (AD) (HC vs. AD: 6.958 vs. 5.462,
< 0.001). Healthy individuals exhibit more complex macroscopic structures and non-random spatiotemporal patterns of microstates, whereas dementia disorders lead to more random spatiotemporal patterns. Additionally, we extend the proposed method by integrating the Complementary Ensemble Empirical Mode Decomposition (CEEMD) method to explore spatiotemporal dynamic patterns of microstates at specific frequency scales. Moreover, we assessed the effectiveness of this innovative method in predicting cognitive scores. The results demonstrate that the incorporation of CEEMD-enhanced microstate dynamic indicators significantly improved the prediction accuracy of Mini-Mental State Examination (MMSE) scores (R
= 0.940). The CEEMD-enhanced MSNRI method not only aids in the exploration of large-scale neural changes in populations with dementia but also offers a robust tool for characterizing the dynamics of EEG microstate transitions and their impact on cognitive function.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>38790465</pmid><doi>10.3390/brainsci14050487</doi><orcidid>https://orcid.org/0000-0003-1887-8631</orcidid><orcidid>https://orcid.org/0000-0003-3666-9833</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Advertising executives Alzheimer's disease Biomarkers Brain research Cognitive ability Datasets Dementia Dementia disorders Disease EEG electroencephalogram Electroencephalography Frontotemporal dementia information-based similarity Medical research Medicine, Experimental Methods microstate transitions Neurodegenerative diseases non-randomness Recording sessions |
title | Beyond Frequency Bands: Complementary-Ensemble-Empirical-Mode-Decomposition-Enhanced Microstate Sequence Non-Randomness Analysis for Aiding Diagnosis and Cognitive Prediction of Dementia |
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