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Nonlinear changes in delayed functional network topology in Alzheimer's disease: relationship with amyloid and tau pathology
Alzheimer's disease is a neurodegenerative disorder associated with the abnormal deposition of pathological processes, such as amyloid-ß and tau, which produces nonlinear changes in the functional connectivity patterns between different brain regions across the Alzheimer's disease continuu...
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Published in: | Alzheimer's research & therapy 2023-06, Vol.15 (1), p.112-112, Article 112 |
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description | Alzheimer's disease is a neurodegenerative disorder associated with the abnormal deposition of pathological processes, such as amyloid-ß and tau, which produces nonlinear changes in the functional connectivity patterns between different brain regions across the Alzheimer's disease continuum. However, the mechanisms underlying these nonlinear changes remain largely unknown. Here, we address this question using a novel method based on temporal or delayed correlations and calculate new whole-brain functional networks to tackle these mechanisms.
To assess our method, we evaluated 166 individuals from the ADNI database, including amyloid-beta negative and positive cognitively normal subjects, patients with mild cognitive impairment, and patients with Alzheimer's disease dementia. We used the clustering coefficient and the global efficiency to measure the functional network topology and assessed their relationship with amyloid and tau pathology measured by positron emission tomography, as well as cognitive performance using tests measuring memory, executive function, attention, and global cognition.
Our study found nonlinear changes in the global efficiency, but not in the clustering coefficient, showing that the nonlinear changes in functional connectivity are due to an altered ability of brain regions to communicate with each other through direct paths. These changes in global efficiency were most prominent in early disease stages. However, later stages of Alzheimer's disease were associated with widespread network disruptions characterized by changes in both network measures. The temporal delays required for the detection of these changes varied across the Alzheimer's disease continuum, with shorter delays necessary to detect changes in early stages and longer delays necessary to detect changes in late stages. Both global efficiency and clustering coefficient showed quadratic associations with pathological amyloid and tau burden as well as cognitive decline.
This study suggests that global efficiency is a more sensitive indicator of network changes in Alzheimer's disease when compared to clustering coefficient. Both network properties were associated with pathology and cognitive performance, demonstrating their relevance in clinical settings. Our findings provide an insight into the mechanisms underlying nonlinear changes in functional network organization in Alzheimer's disease, suggesting that it is the lack of direct connections that drives these functiona |
doi_str_mv | 10.1186/s13195-023-01252-3 |
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To assess our method, we evaluated 166 individuals from the ADNI database, including amyloid-beta negative and positive cognitively normal subjects, patients with mild cognitive impairment, and patients with Alzheimer's disease dementia. We used the clustering coefficient and the global efficiency to measure the functional network topology and assessed their relationship with amyloid and tau pathology measured by positron emission tomography, as well as cognitive performance using tests measuring memory, executive function, attention, and global cognition.
Our study found nonlinear changes in the global efficiency, but not in the clustering coefficient, showing that the nonlinear changes in functional connectivity are due to an altered ability of brain regions to communicate with each other through direct paths. These changes in global efficiency were most prominent in early disease stages. However, later stages of Alzheimer's disease were associated with widespread network disruptions characterized by changes in both network measures. The temporal delays required for the detection of these changes varied across the Alzheimer's disease continuum, with shorter delays necessary to detect changes in early stages and longer delays necessary to detect changes in late stages. Both global efficiency and clustering coefficient showed quadratic associations with pathological amyloid and tau burden as well as cognitive decline.
This study suggests that global efficiency is a more sensitive indicator of network changes in Alzheimer's disease when compared to clustering coefficient. Both network properties were associated with pathology and cognitive performance, demonstrating their relevance in clinical settings. Our findings provide an insight into the mechanisms underlying nonlinear changes in functional network organization in Alzheimer's disease, suggesting that it is the lack of direct connections that drives these functional changes.</description><identifier>ISSN: 1758-9193</identifier><identifier>EISSN: 1758-9193</identifier><identifier>DOI: 10.1186/s13195-023-01252-3</identifier><identifier>PMID: 37328909</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Alzheimer Disease - pathology ; Alzheimer's disease ; Amyloid ; Amyloid beta-Peptides - metabolism ; Amyloid beta-protein ; Anti-symmetric correlations ; Biomarkers ; Brain - metabolism ; Brain research ; Cognitive ability ; Cognitive Dysfunction - diagnostic imaging ; Cognitive Dysfunction - pathology ; Communication ; Delayed connectivity ; Dementia ; Development and progression ; Directed connectivity ; Efficiency ; Functional integration ; Functional MRI ; Health aspects ; Humans ; Magnetic resonance imaging ; Magnetic Resonance Imaging - methods ; Medicin och hälsovetenskap ; Neural circuitry ; Nonlinear functional connectivity ; Pathology ; Physiological aspects ; Positron-Emission Tomography ; Tau proteins ; tau Proteins - metabolism</subject><ispartof>Alzheimer's research & therapy, 2023-06, Vol.15 (1), p.112-112, Article 112</ispartof><rights>2023. The Author(s).</rights><rights>COPYRIGHT 2023 BioMed Central Ltd.</rights><rights>2023. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c721t-92f60875fd869141b5a01e989b6febb4b085d5127c244a61c22afe96390a9ad83</citedby><cites>FETCH-LOGICAL-c721t-92f60875fd869141b5a01e989b6febb4b085d5127c244a61c22afe96390a9ad83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10273754/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2827110699?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37328909$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:152961088$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Mijalkov, Mite</creatorcontrib><creatorcontrib>Veréb, Dániel</creatorcontrib><creatorcontrib>Canal-Garcia, Anna</creatorcontrib><creatorcontrib>Hinault, Thomas</creatorcontrib><creatorcontrib>Volpe, Giovanni</creatorcontrib><creatorcontrib>Pereira, Joana B</creatorcontrib><creatorcontrib>Alzheimer’s Disease Neuroimaging Initiative</creatorcontrib><creatorcontrib>for the Alzheimer’s Disease Neuroimaging Initiative</creatorcontrib><title>Nonlinear changes in delayed functional network topology in Alzheimer's disease: relationship with amyloid and tau pathology</title><title>Alzheimer's research & therapy</title><addtitle>Alzheimers Res Ther</addtitle><description>Alzheimer's disease is a neurodegenerative disorder associated with the abnormal deposition of pathological processes, such as amyloid-ß and tau, which produces nonlinear changes in the functional connectivity patterns between different brain regions across the Alzheimer's disease continuum. However, the mechanisms underlying these nonlinear changes remain largely unknown. Here, we address this question using a novel method based on temporal or delayed correlations and calculate new whole-brain functional networks to tackle these mechanisms.
To assess our method, we evaluated 166 individuals from the ADNI database, including amyloid-beta negative and positive cognitively normal subjects, patients with mild cognitive impairment, and patients with Alzheimer's disease dementia. We used the clustering coefficient and the global efficiency to measure the functional network topology and assessed their relationship with amyloid and tau pathology measured by positron emission tomography, as well as cognitive performance using tests measuring memory, executive function, attention, and global cognition.
Our study found nonlinear changes in the global efficiency, but not in the clustering coefficient, showing that the nonlinear changes in functional connectivity are due to an altered ability of brain regions to communicate with each other through direct paths. These changes in global efficiency were most prominent in early disease stages. However, later stages of Alzheimer's disease were associated with widespread network disruptions characterized by changes in both network measures. The temporal delays required for the detection of these changes varied across the Alzheimer's disease continuum, with shorter delays necessary to detect changes in early stages and longer delays necessary to detect changes in late stages. Both global efficiency and clustering coefficient showed quadratic associations with pathological amyloid and tau burden as well as cognitive decline.
This study suggests that global efficiency is a more sensitive indicator of network changes in Alzheimer's disease when compared to clustering coefficient. Both network properties were associated with pathology and cognitive performance, demonstrating their relevance in clinical settings. Our findings provide an insight into the mechanisms underlying nonlinear changes in functional network organization in Alzheimer's disease, suggesting that it is the lack of direct connections that drives these functional changes.</description><subject>Alzheimer Disease - pathology</subject><subject>Alzheimer's disease</subject><subject>Amyloid</subject><subject>Amyloid beta-Peptides - metabolism</subject><subject>Amyloid beta-protein</subject><subject>Anti-symmetric correlations</subject><subject>Biomarkers</subject><subject>Brain - metabolism</subject><subject>Brain research</subject><subject>Cognitive ability</subject><subject>Cognitive Dysfunction - diagnostic imaging</subject><subject>Cognitive Dysfunction - pathology</subject><subject>Communication</subject><subject>Delayed connectivity</subject><subject>Dementia</subject><subject>Development and progression</subject><subject>Directed connectivity</subject><subject>Efficiency</subject><subject>Functional integration</subject><subject>Functional MRI</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Magnetic resonance imaging</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Medicin och hälsovetenskap</subject><subject>Neural circuitry</subject><subject>Nonlinear functional connectivity</subject><subject>Pathology</subject><subject>Physiological aspects</subject><subject>Positron-Emission Tomography</subject><subject>Tau proteins</subject><subject>tau Proteins - metabolism</subject><issn>1758-9193</issn><issn>1758-9193</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptks1u1DAUhSMEolB4ARbIEhKwSfFPnNhsUFXxU6mCDaytm_hm4tZjD3ZCNYiHJ5kppYNQFMW6-c6XxDlF8YzRE8ZU_SYzwbQsKRclZVzyUtwrHrFGqlIzLe7fWR8Vj3O-pLSuuaoeFkeiEVxpqh8Vvz7H4F1ASKQbIKwwExeIRQ9btKSfQje6GMCTgON1TFdkjJvo42q7YKf-54BujelVJtZlhIxvSZqzSyYPbkOu3TgQWG99dJZAsGSEiWxgHHaOJ8WDHnzGpzfX4-Lbh_dfzz6VF18-np-dXpRdw9lYat7XVDWyt6rWrGKtBMpQK93WPbZt1VIlrWS86XhVQc06zqFHXQtNQYNV4rg433tthEuzSW4NaWsiOLMbxLQykEbXeTSadpWoQHOpeCV60MJKVTXQogQrbTu79N6Vr3EztQe2TYrW3Myv3HKajIZJrmtG1fIe7_bZGVij7TCMCfyh4uBOcINZxR-GUd6IRlaz4fWNIcXvE-bRrF3u0HsIGKdsuOINl1pLOqMv_kEv45TmX7mnGKO11n-pFcxf70If5wd3i9ScNlLwmjIlZurkP9R8WFy7Lgbs3Tw_CLy8ExgQ_Djk6KddMQ5Bvge7FHNO2N_uBqNmabnZt9zMLTe7lpsl9PzuPt5G_tRa_AbeE_h5</recordid><startdate>20230616</startdate><enddate>20230616</enddate><creator>Mijalkov, Mite</creator><creator>Veréb, Dániel</creator><creator>Canal-Garcia, Anna</creator><creator>Hinault, Thomas</creator><creator>Volpe, Giovanni</creator><creator>Pereira, Joana B</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>ZZAVC</scope><scope>DOA</scope></search><sort><creationdate>20230616</creationdate><title>Nonlinear changes in delayed functional network topology in Alzheimer's disease: relationship with amyloid and tau pathology</title><author>Mijalkov, Mite ; Veréb, Dániel ; Canal-Garcia, Anna ; Hinault, Thomas ; Volpe, Giovanni ; Pereira, Joana B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c721t-92f60875fd869141b5a01e989b6febb4b085d5127c244a61c22afe96390a9ad83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Alzheimer Disease - 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metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mijalkov, Mite</creatorcontrib><creatorcontrib>Veréb, Dániel</creatorcontrib><creatorcontrib>Canal-Garcia, Anna</creatorcontrib><creatorcontrib>Hinault, Thomas</creatorcontrib><creatorcontrib>Volpe, Giovanni</creatorcontrib><creatorcontrib>Pereira, Joana B</creatorcontrib><creatorcontrib>Alzheimer’s Disease Neuroimaging Initiative</creatorcontrib><creatorcontrib>for the Alzheimer’s Disease Neuroimaging Initiative</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SwePub Articles full text</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Alzheimer's research & therapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mijalkov, Mite</au><au>Veréb, Dániel</au><au>Canal-Garcia, Anna</au><au>Hinault, Thomas</au><au>Volpe, Giovanni</au><au>Pereira, Joana B</au><aucorp>Alzheimer’s Disease Neuroimaging Initiative</aucorp><aucorp>for the Alzheimer’s Disease Neuroimaging Initiative</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nonlinear changes in delayed functional network topology in Alzheimer's disease: relationship with amyloid and tau pathology</atitle><jtitle>Alzheimer's research & therapy</jtitle><addtitle>Alzheimers Res Ther</addtitle><date>2023-06-16</date><risdate>2023</risdate><volume>15</volume><issue>1</issue><spage>112</spage><epage>112</epage><pages>112-112</pages><artnum>112</artnum><issn>1758-9193</issn><eissn>1758-9193</eissn><abstract>Alzheimer's disease is a neurodegenerative disorder associated with the abnormal deposition of pathological processes, such as amyloid-ß and tau, which produces nonlinear changes in the functional connectivity patterns between different brain regions across the Alzheimer's disease continuum. However, the mechanisms underlying these nonlinear changes remain largely unknown. Here, we address this question using a novel method based on temporal or delayed correlations and calculate new whole-brain functional networks to tackle these mechanisms.
To assess our method, we evaluated 166 individuals from the ADNI database, including amyloid-beta negative and positive cognitively normal subjects, patients with mild cognitive impairment, and patients with Alzheimer's disease dementia. We used the clustering coefficient and the global efficiency to measure the functional network topology and assessed their relationship with amyloid and tau pathology measured by positron emission tomography, as well as cognitive performance using tests measuring memory, executive function, attention, and global cognition.
Our study found nonlinear changes in the global efficiency, but not in the clustering coefficient, showing that the nonlinear changes in functional connectivity are due to an altered ability of brain regions to communicate with each other through direct paths. These changes in global efficiency were most prominent in early disease stages. However, later stages of Alzheimer's disease were associated with widespread network disruptions characterized by changes in both network measures. The temporal delays required for the detection of these changes varied across the Alzheimer's disease continuum, with shorter delays necessary to detect changes in early stages and longer delays necessary to detect changes in late stages. Both global efficiency and clustering coefficient showed quadratic associations with pathological amyloid and tau burden as well as cognitive decline.
This study suggests that global efficiency is a more sensitive indicator of network changes in Alzheimer's disease when compared to clustering coefficient. Both network properties were associated with pathology and cognitive performance, demonstrating their relevance in clinical settings. Our findings provide an insight into the mechanisms underlying nonlinear changes in functional network organization in Alzheimer's disease, suggesting that it is the lack of direct connections that drives these functional changes.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>37328909</pmid><doi>10.1186/s13195-023-01252-3</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Alzheimer Disease - pathology Alzheimer's disease Amyloid Amyloid beta-Peptides - metabolism Amyloid beta-protein Anti-symmetric correlations Biomarkers Brain - metabolism Brain research Cognitive ability Cognitive Dysfunction - diagnostic imaging Cognitive Dysfunction - pathology Communication Delayed connectivity Dementia Development and progression Directed connectivity Efficiency Functional integration Functional MRI Health aspects Humans Magnetic resonance imaging Magnetic Resonance Imaging - methods Medicin och hälsovetenskap Neural circuitry Nonlinear functional connectivity Pathology Physiological aspects Positron-Emission Tomography Tau proteins tau Proteins - metabolism |
title | Nonlinear changes in delayed functional network topology in Alzheimer's disease: relationship with amyloid and tau pathology |
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