Challenges and Opportunities with Causal Discovery Algorithms: Application to Alzheimer’s Pathophysiology
Causal Structure Discovery (CSD) is the problem of identifying causal relationships from large quantities of data through computational methods. With the limited ability of traditional association-based computational methods to discover causal relationships, CSD methodologies are gaining popularity....
Gespeichert in:
Veröffentlicht in: | Scientific reports 2020-02, Vol.10 (1), p.2975-2975, Article 2975 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 2975 |
---|---|
container_issue | 1 |
container_start_page | 2975 |
container_title | Scientific reports |
container_volume | 10 |
creator | Shen, Xinpeng Ma, Sisi Vemuri, Prashanthi Simon, Gyorgy |
description | Causal Structure Discovery (CSD) is the problem of identifying causal relationships from large quantities of data through computational methods. With the limited ability of traditional association-based computational methods to discover causal relationships, CSD methodologies are gaining popularity. The goal of the study was to systematically examine whether (i) CSD methods can discover the known causal relationships from observational clinical data and (ii) to offer guidance to accurately discover known causal relationships. We used Alzheimer’s disease (AD), a complex progressive disease, as a model because the well-established evidence provides a “gold-standard” causal graph for evaluation. We evaluated two CSD methods, Fast Causal Inference (FCI) and Fast Greedy Equivalence Search (FGES) in their ability to discover this structure from data collected by the Alzheimer’s Disease Neuroimaging Initiative (ADNI). We used structural equation models (which is not designed for CSD) as control. We applied these methods under three scenarios defined by increasing amounts of background knowledge provided to the methods. The methods were evaluated by comparing the resulting causal relationships with the “gold standard” graph that was constructed from literature. Dedicated CSD methods managed to discover graphs that nearly coincided with the gold standard. For best results, CSD algorithms should be used with longitudinal data providing as much prior knowledge as possible. |
doi_str_mv | 10.1038/s41598-020-59669-x |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7031278</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2359397116</sourcerecordid><originalsourceid>FETCH-LOGICAL-c474t-eb29d983f6442b19b9267e7b5d961579ed5da63768498917997468a9b7c036fe3</originalsourceid><addsrcrecordid>eNp9kc1u1DAUhS0EolXpC7BAkdiwCfjfuSyQRgMFpEplAWvLSTwTFycOtlM6rPoavB5PgsuUUljgjS2f7557rw5Cjwl-TjBrXiROBDQ1prgWICXUl_fQIcVc1JRRev_O-wAdp3SOyxEUOIGH6IBRrGQpPUSf14Px3k5bmyoz9dXZPIeYl8llV36-ujxUa7Mk46vXLnXhwsZdtfLbEIsyppfVap6960x2YapyKNK3wbrRxh9X31P1weQhzMMuueDDdvcIPdgYn-zxzX2EPp28-bh-V5-evX2_Xp3WHVc817al0EPDNpJz2hJogUplVSt6kEQosL3ojWRKNhwaIApAcdkYaFWHmdxYdoRe7X3npR1t39kpR-P1HN1o4k4H4_TfyuQGvQ0XWmFGqGqKwbMbgxi-LDZlPZblrfdmsmFJmjIBDBQhsqBP_0HPwxKnst411YgyGYZC0T3VxZBStJvbYQjW13HqfZy6ZKJ_xakvS9GTu2vclvwOrwBsD6QilQTjn97_sf0J1VOuHw</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2358546809</pqid></control><display><type>article</type><title>Challenges and Opportunities with Causal Discovery Algorithms: Application to Alzheimer’s Pathophysiology</title><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Springer Nature OA Free Journals</source><source>Nature Free</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><source>Free Full-Text Journals in Chemistry</source><creator>Shen, Xinpeng ; Ma, Sisi ; Vemuri, Prashanthi ; Simon, Gyorgy</creator><creatorcontrib>Shen, Xinpeng ; Ma, Sisi ; Vemuri, Prashanthi ; Simon, Gyorgy ; Alzheimer’s Disease Neuroimaging Initiative ; the Alzheimer’s Disease Neuroimaging Initiative</creatorcontrib><description>Causal Structure Discovery (CSD) is the problem of identifying causal relationships from large quantities of data through computational methods. With the limited ability of traditional association-based computational methods to discover causal relationships, CSD methodologies are gaining popularity. The goal of the study was to systematically examine whether (i) CSD methods can discover the known causal relationships from observational clinical data and (ii) to offer guidance to accurately discover known causal relationships. We used Alzheimer’s disease (AD), a complex progressive disease, as a model because the well-established evidence provides a “gold-standard” causal graph for evaluation. We evaluated two CSD methods, Fast Causal Inference (FCI) and Fast Greedy Equivalence Search (FGES) in their ability to discover this structure from data collected by the Alzheimer’s Disease Neuroimaging Initiative (ADNI). We used structural equation models (which is not designed for CSD) as control. We applied these methods under three scenarios defined by increasing amounts of background knowledge provided to the methods. The methods were evaluated by comparing the resulting causal relationships with the “gold standard” graph that was constructed from literature. Dedicated CSD methods managed to discover graphs that nearly coincided with the gold standard. For best results, CSD algorithms should be used with longitudinal data providing as much prior knowledge as possible.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-020-59669-x</identifier><identifier>PMID: 32076020</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/378/2612 ; 692/617/375/132/1283 ; Aged ; Aged, 80 and over ; Algorithms ; Alzheimer Disease - diagnosis ; Alzheimer Disease - etiology ; Alzheimer Disease - pathology ; Alzheimer's disease ; Amyloid beta-Peptides - analysis ; Apolipoprotein E4 - genetics ; Apolipoproteins E - genetics ; Biomarkers - analysis ; Brain - diagnostic imaging ; Brain - pathology ; Computational neuroscience ; Data Interpretation, Statistical ; Datasets as Topic ; Female ; Humanities and Social Sciences ; Humans ; Latent Class Analysis ; Longitudinal Studies ; Magnetic Resonance Imaging - statistics & numerical data ; Male ; Models, Neurological ; multidisciplinary ; Neurodegenerative diseases ; Neuroimaging ; Neuroimaging - statistics & numerical data ; Observational Studies as Topic ; Positron-Emission Tomography - statistics & numerical data ; Science ; Science (multidisciplinary) ; tau Proteins - analysis</subject><ispartof>Scientific reports, 2020-02, Vol.10 (1), p.2975-2975, Article 2975</ispartof><rights>The Author(s) 2020</rights><rights>This work is published 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><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-eb29d983f6442b19b9267e7b5d961579ed5da63768498917997468a9b7c036fe3</citedby><cites>FETCH-LOGICAL-c474t-eb29d983f6442b19b9267e7b5d961579ed5da63768498917997468a9b7c036fe3</cites><orcidid>0000-0003-1191-0010</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7031278/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7031278/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,861,882,27905,27906,41101,42170,51557,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32076020$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shen, Xinpeng</creatorcontrib><creatorcontrib>Ma, Sisi</creatorcontrib><creatorcontrib>Vemuri, Prashanthi</creatorcontrib><creatorcontrib>Simon, Gyorgy</creatorcontrib><creatorcontrib>Alzheimer’s Disease Neuroimaging Initiative</creatorcontrib><creatorcontrib>the Alzheimer’s Disease Neuroimaging Initiative</creatorcontrib><title>Challenges and Opportunities with Causal Discovery Algorithms: Application to Alzheimer’s Pathophysiology</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Causal Structure Discovery (CSD) is the problem of identifying causal relationships from large quantities of data through computational methods. With the limited ability of traditional association-based computational methods to discover causal relationships, CSD methodologies are gaining popularity. The goal of the study was to systematically examine whether (i) CSD methods can discover the known causal relationships from observational clinical data and (ii) to offer guidance to accurately discover known causal relationships. We used Alzheimer’s disease (AD), a complex progressive disease, as a model because the well-established evidence provides a “gold-standard” causal graph for evaluation. We evaluated two CSD methods, Fast Causal Inference (FCI) and Fast Greedy Equivalence Search (FGES) in their ability to discover this structure from data collected by the Alzheimer’s Disease Neuroimaging Initiative (ADNI). We used structural equation models (which is not designed for CSD) as control. We applied these methods under three scenarios defined by increasing amounts of background knowledge provided to the methods. The methods were evaluated by comparing the resulting causal relationships with the “gold standard” graph that was constructed from literature. Dedicated CSD methods managed to discover graphs that nearly coincided with the gold standard. For best results, CSD algorithms should be used with longitudinal data providing as much prior knowledge as possible.</description><subject>631/378/2612</subject><subject>692/617/375/132/1283</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Algorithms</subject><subject>Alzheimer Disease - diagnosis</subject><subject>Alzheimer Disease - etiology</subject><subject>Alzheimer Disease - pathology</subject><subject>Alzheimer's disease</subject><subject>Amyloid beta-Peptides - analysis</subject><subject>Apolipoprotein E4 - genetics</subject><subject>Apolipoproteins E - genetics</subject><subject>Biomarkers - analysis</subject><subject>Brain - diagnostic imaging</subject><subject>Brain - pathology</subject><subject>Computational neuroscience</subject><subject>Data Interpretation, Statistical</subject><subject>Datasets as Topic</subject><subject>Female</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Latent Class Analysis</subject><subject>Longitudinal Studies</subject><subject>Magnetic Resonance Imaging - statistics & numerical data</subject><subject>Male</subject><subject>Models, Neurological</subject><subject>multidisciplinary</subject><subject>Neurodegenerative diseases</subject><subject>Neuroimaging</subject><subject>Neuroimaging - statistics & numerical data</subject><subject>Observational Studies as Topic</subject><subject>Positron-Emission Tomography - statistics & numerical data</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>tau Proteins - analysis</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kc1u1DAUhS0EolXpC7BAkdiwCfjfuSyQRgMFpEplAWvLSTwTFycOtlM6rPoavB5PgsuUUljgjS2f7557rw5Cjwl-TjBrXiROBDQ1prgWICXUl_fQIcVc1JRRev_O-wAdp3SOyxEUOIGH6IBRrGQpPUSf14Px3k5bmyoz9dXZPIeYl8llV36-ujxUa7Mk46vXLnXhwsZdtfLbEIsyppfVap6960x2YapyKNK3wbrRxh9X31P1weQhzMMuueDDdvcIPdgYn-zxzX2EPp28-bh-V5-evX2_Xp3WHVc817al0EPDNpJz2hJogUplVSt6kEQosL3ojWRKNhwaIApAcdkYaFWHmdxYdoRe7X3npR1t39kpR-P1HN1o4k4H4_TfyuQGvQ0XWmFGqGqKwbMbgxi-LDZlPZblrfdmsmFJmjIBDBQhsqBP_0HPwxKnst411YgyGYZC0T3VxZBStJvbYQjW13HqfZy6ZKJ_xakvS9GTu2vclvwOrwBsD6QilQTjn97_sf0J1VOuHw</recordid><startdate>20200219</startdate><enddate>20200219</enddate><creator>Shen, Xinpeng</creator><creator>Ma, Sisi</creator><creator>Vemuri, Prashanthi</creator><creator>Simon, Gyorgy</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><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>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-1191-0010</orcidid></search><sort><creationdate>20200219</creationdate><title>Challenges and Opportunities with Causal Discovery Algorithms: Application to Alzheimer’s Pathophysiology</title><author>Shen, Xinpeng ; Ma, Sisi ; Vemuri, Prashanthi ; Simon, Gyorgy</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-eb29d983f6442b19b9267e7b5d961579ed5da63768498917997468a9b7c036fe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>631/378/2612</topic><topic>692/617/375/132/1283</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Algorithms</topic><topic>Alzheimer Disease - diagnosis</topic><topic>Alzheimer Disease - etiology</topic><topic>Alzheimer Disease - pathology</topic><topic>Alzheimer's disease</topic><topic>Amyloid beta-Peptides - analysis</topic><topic>Apolipoprotein E4 - genetics</topic><topic>Apolipoproteins E - genetics</topic><topic>Biomarkers - analysis</topic><topic>Brain - diagnostic imaging</topic><topic>Brain - pathology</topic><topic>Computational neuroscience</topic><topic>Data Interpretation, Statistical</topic><topic>Datasets as Topic</topic><topic>Female</topic><topic>Humanities and Social Sciences</topic><topic>Humans</topic><topic>Latent Class Analysis</topic><topic>Longitudinal Studies</topic><topic>Magnetic Resonance Imaging - statistics & numerical data</topic><topic>Male</topic><topic>Models, Neurological</topic><topic>multidisciplinary</topic><topic>Neurodegenerative diseases</topic><topic>Neuroimaging</topic><topic>Neuroimaging - statistics & numerical data</topic><topic>Observational Studies as Topic</topic><topic>Positron-Emission Tomography - statistics & numerical data</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>tau Proteins - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shen, Xinpeng</creatorcontrib><creatorcontrib>Ma, Sisi</creatorcontrib><creatorcontrib>Vemuri, Prashanthi</creatorcontrib><creatorcontrib>Simon, Gyorgy</creatorcontrib><creatorcontrib>Alzheimer’s Disease Neuroimaging Initiative</creatorcontrib><creatorcontrib>the Alzheimer’s Disease Neuroimaging Initiative</creatorcontrib><collection>Springer Nature OA Free Journals</collection><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>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</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 Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science 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 Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shen, Xinpeng</au><au>Ma, Sisi</au><au>Vemuri, Prashanthi</au><au>Simon, Gyorgy</au><aucorp>Alzheimer’s Disease Neuroimaging Initiative</aucorp><aucorp>the Alzheimer’s Disease Neuroimaging Initiative</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Challenges and Opportunities with Causal Discovery Algorithms: Application to Alzheimer’s Pathophysiology</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2020-02-19</date><risdate>2020</risdate><volume>10</volume><issue>1</issue><spage>2975</spage><epage>2975</epage><pages>2975-2975</pages><artnum>2975</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Causal Structure Discovery (CSD) is the problem of identifying causal relationships from large quantities of data through computational methods. With the limited ability of traditional association-based computational methods to discover causal relationships, CSD methodologies are gaining popularity. The goal of the study was to systematically examine whether (i) CSD methods can discover the known causal relationships from observational clinical data and (ii) to offer guidance to accurately discover known causal relationships. We used Alzheimer’s disease (AD), a complex progressive disease, as a model because the well-established evidence provides a “gold-standard” causal graph for evaluation. We evaluated two CSD methods, Fast Causal Inference (FCI) and Fast Greedy Equivalence Search (FGES) in their ability to discover this structure from data collected by the Alzheimer’s Disease Neuroimaging Initiative (ADNI). We used structural equation models (which is not designed for CSD) as control. We applied these methods under three scenarios defined by increasing amounts of background knowledge provided to the methods. The methods were evaluated by comparing the resulting causal relationships with the “gold standard” graph that was constructed from literature. Dedicated CSD methods managed to discover graphs that nearly coincided with the gold standard. For best results, CSD algorithms should be used with longitudinal data providing as much prior knowledge as possible.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>32076020</pmid><doi>10.1038/s41598-020-59669-x</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-1191-0010</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2045-2322 |
ispartof | Scientific reports, 2020-02, Vol.10 (1), p.2975-2975, Article 2975 |
issn | 2045-2322 2045-2322 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7031278 |
source | MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Springer Nature OA Free Journals; Nature Free; PubMed Central; Alma/SFX Local Collection; Free Full-Text Journals in Chemistry |
subjects | 631/378/2612 692/617/375/132/1283 Aged Aged, 80 and over Algorithms Alzheimer Disease - diagnosis Alzheimer Disease - etiology Alzheimer Disease - pathology Alzheimer's disease Amyloid beta-Peptides - analysis Apolipoprotein E4 - genetics Apolipoproteins E - genetics Biomarkers - analysis Brain - diagnostic imaging Brain - pathology Computational neuroscience Data Interpretation, Statistical Datasets as Topic Female Humanities and Social Sciences Humans Latent Class Analysis Longitudinal Studies Magnetic Resonance Imaging - statistics & numerical data Male Models, Neurological multidisciplinary Neurodegenerative diseases Neuroimaging Neuroimaging - statistics & numerical data Observational Studies as Topic Positron-Emission Tomography - statistics & numerical data Science Science (multidisciplinary) tau Proteins - analysis |
title | Challenges and Opportunities with Causal Discovery Algorithms: Application to Alzheimer’s Pathophysiology |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-18T17%3A33%3A30IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Challenges%20and%20Opportunities%20with%20Causal%20Discovery%20Algorithms:%20Application%20to%20Alzheimer%E2%80%99s%20Pathophysiology&rft.jtitle=Scientific%20reports&rft.au=Shen,%20Xinpeng&rft.aucorp=Alzheimer%E2%80%99s%20Disease%20Neuroimaging%20Initiative&rft.date=2020-02-19&rft.volume=10&rft.issue=1&rft.spage=2975&rft.epage=2975&rft.pages=2975-2975&rft.artnum=2975&rft.issn=2045-2322&rft.eissn=2045-2322&rft_id=info:doi/10.1038/s41598-020-59669-x&rft_dat=%3Cproquest_pubme%3E2359397116%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2358546809&rft_id=info:pmid/32076020&rfr_iscdi=true |