DEMENTIA DUE TO ALZHEIMER’S DISEASE AND BRAIN MORPHOMETRIC ALTERATIONS

Introduction: Dementia due Alzheimer’s disease (DAD) is a primary and progressive neurodegenerative disorder. There are atrophy in hippocampus and other basal areas. This work evaluated the brain morphometry of DAD patients in all disease stages, aiming at identifying the structural neuro-degenerati...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Innovation in aging 2017-07, Vol.1 (suppl_1), p.350-350
Hauptverfasser: Moriguti, J.C., Silva Filho, S.R., Santos, A.C., Ferriolli, E., Lima, N.K.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 350
container_issue suppl_1
container_start_page 350
container_title Innovation in aging
container_volume 1
creator Moriguti, J.C.
Silva Filho, S.R.
Santos, A.C.
Ferriolli, E.
Lima, N.K.
description Introduction: Dementia due Alzheimer’s disease (DAD) is a primary and progressive neurodegenerative disorder. There are atrophy in hippocampus and other basal areas. This work evaluated the brain morphometry of DAD patients in all disease stages, aiming at identifying the structural neuro-degeneration profile in every phase. Methods: DAD patients above 60 years old (n=44) and age paired controls (n=16) were recruited. The brain images acquired in Achieva 3T magnetic resonance tomograph. Volumetric quantitative data and cortical thickness measurements were obtained by automatic segmentation using Freesurfer®. The volume of each region was normalized considering whole brain volume. Results: Brain regions targeted by the disease during the initial stages were found to be altered until in the later stages of the dementia. No correlation was observed between brain cortical volume or thickness, age and years of education. We found an association between cortical volume or thickness and cognitive indexes Mini Mental State Examination (R 2
doi_str_mv 10.1093/geroni/igx004.1280
format Article
fullrecord <record><control><sourceid>pubmedcentral_cross</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6244175</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>pubmedcentral_primary_oai_pubmedcentral_nih_gov_6244175</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1420-f941a1e6da1fbd5cc756dbee548ecd7a5345817023f7d8d34df99a4fe9c4db63</originalsourceid><addsrcrecordid>eNpVkNFOgzAYhRujicvcC3jFC7C1tAV6Y4KjSpMBBuqNN02hZWK2sYAavfM1fD2fxC0Yo1f_Sf5zvosPgEsE5wgyvFjbvtu1i3b9BiGZIy-EJ2DiYcZciiE8_ZPPwWwYniCEiGHCiDcBScxTnkkROfE9d2TuRKuHhIuUF18fn6UTi5JHJXeiLHaui0hkTpoXd0meclmI5aEseRFJkWflBThr9Gaws587BfKGy2XirvJbsYxWbo2IB92GEaSR9Y1GTWVoXQfUN5W1lIS2NoGmmNAQBdDDTWBCg4lpGNOksawmpvLxFFyN2P1LtbWmtrvnXm_Uvm-3un9XnW7V_8-ufVTr7lX5HiEooAeANwLqvhuG3ja_WwTVUacadapRpzrqxN_-9Gfy</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>DEMENTIA DUE TO ALZHEIMER’S DISEASE AND BRAIN MORPHOMETRIC ALTERATIONS</title><source>Oxford Journals Open Access Collection</source><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><creator>Moriguti, J.C. ; Silva Filho, S.R. ; Santos, A.C. ; Ferriolli, E. ; Lima, N.K.</creator><creatorcontrib>Moriguti, J.C. ; Silva Filho, S.R. ; Santos, A.C. ; Ferriolli, E. ; Lima, N.K.</creatorcontrib><description>Introduction: Dementia due Alzheimer’s disease (DAD) is a primary and progressive neurodegenerative disorder. There are atrophy in hippocampus and other basal areas. This work evaluated the brain morphometry of DAD patients in all disease stages, aiming at identifying the structural neuro-degeneration profile in every phase. Methods: DAD patients above 60 years old (n=44) and age paired controls (n=16) were recruited. The brain images acquired in Achieva 3T magnetic resonance tomograph. Volumetric quantitative data and cortical thickness measurements were obtained by automatic segmentation using Freesurfer®. The volume of each region was normalized considering whole brain volume. Results: Brain regions targeted by the disease during the initial stages were found to be altered until in the later stages of the dementia. No correlation was observed between brain cortical volume or thickness, age and years of education. We found an association between cortical volume or thickness and cognitive indexes Mini Mental State Examination (R 2 &lt;0.47), Clinical Dementia Rating and disease duration in years (R 2 &lt;0.52). Conclusion: The most affected brain regions suffer atrophy in a linear fashion until the later stages of the disease, what seems contrary to the hypothesized models, which consider a faster degeneration in earlier stages. These regions are closely related to neuronal loss and gliosis. The cortical thickness measurements were less sensible in differentiating the groups than cortical volume, what may be due to the fact that cortical thickness is more dependent of segmentation quality. These findings favor a better understanding of the physiopathological process in the advanced diseases stages.</description><identifier>ISSN: 2399-5300</identifier><identifier>EISSN: 2399-5300</identifier><identifier>DOI: 10.1093/geroni/igx004.1280</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Abstracts</subject><ispartof>Innovation in aging, 2017-07, Vol.1 (suppl_1), p.350-350</ispartof><rights>The Author 2017. Published by Oxford University Press on behalf of The Gerontological Society of America. 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244175/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244175/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids></links><search><creatorcontrib>Moriguti, J.C.</creatorcontrib><creatorcontrib>Silva Filho, S.R.</creatorcontrib><creatorcontrib>Santos, A.C.</creatorcontrib><creatorcontrib>Ferriolli, E.</creatorcontrib><creatorcontrib>Lima, N.K.</creatorcontrib><title>DEMENTIA DUE TO ALZHEIMER’S DISEASE AND BRAIN MORPHOMETRIC ALTERATIONS</title><title>Innovation in aging</title><description>Introduction: Dementia due Alzheimer’s disease (DAD) is a primary and progressive neurodegenerative disorder. There are atrophy in hippocampus and other basal areas. This work evaluated the brain morphometry of DAD patients in all disease stages, aiming at identifying the structural neuro-degeneration profile in every phase. Methods: DAD patients above 60 years old (n=44) and age paired controls (n=16) were recruited. The brain images acquired in Achieva 3T magnetic resonance tomograph. Volumetric quantitative data and cortical thickness measurements were obtained by automatic segmentation using Freesurfer®. The volume of each region was normalized considering whole brain volume. Results: Brain regions targeted by the disease during the initial stages were found to be altered until in the later stages of the dementia. No correlation was observed between brain cortical volume or thickness, age and years of education. We found an association between cortical volume or thickness and cognitive indexes Mini Mental State Examination (R 2 &lt;0.47), Clinical Dementia Rating and disease duration in years (R 2 &lt;0.52). Conclusion: The most affected brain regions suffer atrophy in a linear fashion until the later stages of the disease, what seems contrary to the hypothesized models, which consider a faster degeneration in earlier stages. These regions are closely related to neuronal loss and gliosis. The cortical thickness measurements were less sensible in differentiating the groups than cortical volume, what may be due to the fact that cortical thickness is more dependent of segmentation quality. These findings favor a better understanding of the physiopathological process in the advanced diseases stages.</description><subject>Abstracts</subject><issn>2399-5300</issn><issn>2399-5300</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNpVkNFOgzAYhRujicvcC3jFC7C1tAV6Y4KjSpMBBuqNN02hZWK2sYAavfM1fD2fxC0Yo1f_Sf5zvosPgEsE5wgyvFjbvtu1i3b9BiGZIy-EJ2DiYcZciiE8_ZPPwWwYniCEiGHCiDcBScxTnkkROfE9d2TuRKuHhIuUF18fn6UTi5JHJXeiLHaui0hkTpoXd0meclmI5aEseRFJkWflBThr9Gaws587BfKGy2XirvJbsYxWbo2IB92GEaSR9Y1GTWVoXQfUN5W1lIS2NoGmmNAQBdDDTWBCg4lpGNOksawmpvLxFFyN2P1LtbWmtrvnXm_Uvm-3un9XnW7V_8-ufVTr7lX5HiEooAeANwLqvhuG3ja_WwTVUacadapRpzrqxN_-9Gfy</recordid><startdate>20170701</startdate><enddate>20170701</enddate><creator>Moriguti, J.C.</creator><creator>Silva Filho, S.R.</creator><creator>Santos, A.C.</creator><creator>Ferriolli, E.</creator><creator>Lima, N.K.</creator><general>Oxford University Press</general><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20170701</creationdate><title>DEMENTIA DUE TO ALZHEIMER’S DISEASE AND BRAIN MORPHOMETRIC ALTERATIONS</title><author>Moriguti, J.C. ; Silva Filho, S.R. ; Santos, A.C. ; Ferriolli, E. ; Lima, N.K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1420-f941a1e6da1fbd5cc756dbee548ecd7a5345817023f7d8d34df99a4fe9c4db63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Abstracts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Moriguti, J.C.</creatorcontrib><creatorcontrib>Silva Filho, S.R.</creatorcontrib><creatorcontrib>Santos, A.C.</creatorcontrib><creatorcontrib>Ferriolli, E.</creatorcontrib><creatorcontrib>Lima, N.K.</creatorcontrib><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Innovation in aging</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Moriguti, J.C.</au><au>Silva Filho, S.R.</au><au>Santos, A.C.</au><au>Ferriolli, E.</au><au>Lima, N.K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>DEMENTIA DUE TO ALZHEIMER’S DISEASE AND BRAIN MORPHOMETRIC ALTERATIONS</atitle><jtitle>Innovation in aging</jtitle><date>2017-07-01</date><risdate>2017</risdate><volume>1</volume><issue>suppl_1</issue><spage>350</spage><epage>350</epage><pages>350-350</pages><issn>2399-5300</issn><eissn>2399-5300</eissn><abstract>Introduction: Dementia due Alzheimer’s disease (DAD) is a primary and progressive neurodegenerative disorder. There are atrophy in hippocampus and other basal areas. This work evaluated the brain morphometry of DAD patients in all disease stages, aiming at identifying the structural neuro-degeneration profile in every phase. Methods: DAD patients above 60 years old (n=44) and age paired controls (n=16) were recruited. The brain images acquired in Achieva 3T magnetic resonance tomograph. Volumetric quantitative data and cortical thickness measurements were obtained by automatic segmentation using Freesurfer®. The volume of each region was normalized considering whole brain volume. Results: Brain regions targeted by the disease during the initial stages were found to be altered until in the later stages of the dementia. No correlation was observed between brain cortical volume or thickness, age and years of education. We found an association between cortical volume or thickness and cognitive indexes Mini Mental State Examination (R 2 &lt;0.47), Clinical Dementia Rating and disease duration in years (R 2 &lt;0.52). Conclusion: The most affected brain regions suffer atrophy in a linear fashion until the later stages of the disease, what seems contrary to the hypothesized models, which consider a faster degeneration in earlier stages. These regions are closely related to neuronal loss and gliosis. The cortical thickness measurements were less sensible in differentiating the groups than cortical volume, what may be due to the fact that cortical thickness is more dependent of segmentation quality. These findings favor a better understanding of the physiopathological process in the advanced diseases stages.</abstract><cop>US</cop><pub>Oxford University Press</pub><doi>10.1093/geroni/igx004.1280</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2399-5300
ispartof Innovation in aging, 2017-07, Vol.1 (suppl_1), p.350-350
issn 2399-5300
2399-5300
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6244175
source Oxford Journals Open Access Collection; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
subjects Abstracts
title DEMENTIA DUE TO ALZHEIMER’S DISEASE AND BRAIN MORPHOMETRIC ALTERATIONS
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-10T02%3A21%3A10IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmedcentral_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=DEMENTIA%20DUE%20TO%20ALZHEIMER%E2%80%99S%20DISEASE%20AND%20BRAIN%20MORPHOMETRIC%20ALTERATIONS&rft.jtitle=Innovation%20in%20aging&rft.au=Moriguti,%20J.C.&rft.date=2017-07-01&rft.volume=1&rft.issue=suppl_1&rft.spage=350&rft.epage=350&rft.pages=350-350&rft.issn=2399-5300&rft.eissn=2399-5300&rft_id=info:doi/10.1093/geroni/igx004.1280&rft_dat=%3Cpubmedcentral_cross%3Epubmedcentral_primary_oai_pubmedcentral_nih_gov_6244175%3C/pubmedcentral_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true