CSF YKL-40 and pTau181 are related to different cerebral morphometric patterns in early AD
Abstract Cerebrospinal fluid (CSF) concentrations of YKL-40 that serve as biomarker of neuroinflammation are known to be altered along the clinico-biological continuum of Alzheimer's disease (AD). The specific structural cerebral correlates of CSF YKL-40 were evaluated across the early stages o...
Gespeichert in:
Veröffentlicht in: | Neurobiology of aging 2016-02, Vol.38, p.47-55 |
---|---|
Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 55 |
---|---|
container_issue | |
container_start_page | 47 |
container_title | Neurobiology of aging |
container_volume | 38 |
creator | Gispert, Juan Domingo Monté, Gemma C Falcon, Carles Tucholka, Alan Rojas, Santiago Sánchez-Valle, Raquel Antonell, Anna Lladó, Albert Rami, Lorena Molinuevo, José Luis |
description | Abstract Cerebrospinal fluid (CSF) concentrations of YKL-40 that serve as biomarker of neuroinflammation are known to be altered along the clinico-biological continuum of Alzheimer's disease (AD). The specific structural cerebral correlates of CSF YKL-40 were evaluated across the early stages of AD from normal to preclinical to mild dementia. Nonlinear gray matter (GM) volume associations with CSF YKL-40 levels were assessed in a total of 116 subjects, including normal controls and those with preclinical AD as defined by CSF Aβ < 500 pg/mL, mild cognitive impairment (MCI) due to AD, or mild AD dementia. Age-corrected YKL-40 levels were increased in MCIs versus the rest of groups and showed an inverse u-shaped association with p-tau values. A similar nonlinear relationship was found between GM volume and YKL-40 in inferior and lateral temporal regions spreading to the supramarginal gyrus, insula, inferior frontal cortex, and cerebellum in MCI and AD. These findings for YKL-40 remained unchanged after adjusting for p-tau, which was found to be associated with GM volumes in distinct anatomic areas. CSF YKL-40, a biomarker of glial inflammation, is associated with a cerebral structural signature distinct from that related to p-tau neurodegeneration at the earliest stages of cognitive decline due to AD. |
doi_str_mv | 10.1016/j.neurobiolaging.2015.10.022 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1768578667</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0197458015005345</els_id><sourcerecordid>1768578667</sourcerecordid><originalsourceid>FETCH-LOGICAL-c474t-2c48642f468d19504207f7c333328e7e6ccbaaff443503a0afe2e894c5db6dfe3</originalsourceid><addsrcrecordid>eNqNUk2P0zAQtRCI7Rb-AvKBA5cU2_FXJYS0KnRBVOKwywEuluNMFpfEDnaC1H-Poy5IcNq5vMO8mTd6bxB6ScmGEipfHzcB5hQbH3t758PdhhEqSmtDGHuEVlQIXVG-VY_RitCtqrjQ5AJd5nwkhCiu5FN0waRmSnK2Qt92N3v89dOh4gTb0OLx1s5UU2wT4AS9naDFU8St7zpIECbsCjTJ9niIafweB5iSd3i00wQpZOwDBpv6E7569ww96Wyf4fk9rtGX_fvb3Yfq8Pn64-7qUDmu-FQxx3U5peNSt3QrCGdEdcrVpZgGBdK5xtqu47wWpLbEdsBAb7kTbSPbDuo1enXeO6b4c4Y8mcFnB31vA8Q5G6qkFkpLqR5CZaQmvGit0Zsz1aWYc4LOjMkPNp0MJWYJwhzNv0GYJYilW4Io4y_uleZmgPbv8B_nC2F_JkCx5peHZLLzEBy0PoGbTBv9Q5Xe_rfI9T54Z_sfcIJ8jHMKxX5DTWaGmJvlKZafoIIQUXNR_wY40bVf</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1762030444</pqid></control><display><type>article</type><title>CSF YKL-40 and pTau181 are related to different cerebral morphometric patterns in early AD</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Gispert, Juan Domingo ; Monté, Gemma C ; Falcon, Carles ; Tucholka, Alan ; Rojas, Santiago ; Sánchez-Valle, Raquel ; Antonell, Anna ; Lladó, Albert ; Rami, Lorena ; Molinuevo, José Luis</creator><creatorcontrib>Gispert, Juan Domingo ; Monté, Gemma C ; Falcon, Carles ; Tucholka, Alan ; Rojas, Santiago ; Sánchez-Valle, Raquel ; Antonell, Anna ; Lladó, Albert ; Rami, Lorena ; Molinuevo, José Luis</creatorcontrib><description>Abstract Cerebrospinal fluid (CSF) concentrations of YKL-40 that serve as biomarker of neuroinflammation are known to be altered along the clinico-biological continuum of Alzheimer's disease (AD). The specific structural cerebral correlates of CSF YKL-40 were evaluated across the early stages of AD from normal to preclinical to mild dementia. Nonlinear gray matter (GM) volume associations with CSF YKL-40 levels were assessed in a total of 116 subjects, including normal controls and those with preclinical AD as defined by CSF Aβ < 500 pg/mL, mild cognitive impairment (MCI) due to AD, or mild AD dementia. Age-corrected YKL-40 levels were increased in MCIs versus the rest of groups and showed an inverse u-shaped association with p-tau values. A similar nonlinear relationship was found between GM volume and YKL-40 in inferior and lateral temporal regions spreading to the supramarginal gyrus, insula, inferior frontal cortex, and cerebellum in MCI and AD. These findings for YKL-40 remained unchanged after adjusting for p-tau, which was found to be associated with GM volumes in distinct anatomic areas. CSF YKL-40, a biomarker of glial inflammation, is associated with a cerebral structural signature distinct from that related to p-tau neurodegeneration at the earliest stages of cognitive decline due to AD.</description><identifier>ISSN: 0197-4580</identifier><identifier>EISSN: 1558-1497</identifier><identifier>DOI: 10.1016/j.neurobiolaging.2015.10.022</identifier><identifier>PMID: 26827642</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Aged ; Alzheimer Disease - diagnosis ; Alzheimer Disease - pathology ; Amyloid beta-Peptides - cerebrospinal fluid ; Astrocyte ; Astrocytes - pathology ; Astrocytosis ; Astroglia ; Astrogliosis ; Biomarkers - cerebrospinal fluid ; Chitinase-3-Like Protein 1 - cerebrospinal fluid ; Cognitive Dysfunction - diagnosis ; Cognitive Dysfunction - pathology ; Female ; Glia ; Gray Matter - pathology ; Humans ; Inflammation - diagnosis ; Inflammation - pathology ; Internal Medicine ; Magnetic Resonance Imaging ; Magnetic resonance imaging (MRI) ; Male ; Microglia ; Microgliosis ; Middle Aged ; Neuroglia - pathology ; Neuroimaging ; Neuroinflammation ; Neurology ; Tau ; tau Proteins - cerebrospinal fluid ; Voxel-based morphometry (VBM)</subject><ispartof>Neurobiology of aging, 2016-02, Vol.38, p.47-55</ispartof><rights>Elsevier Inc.</rights><rights>2016 Elsevier Inc.</rights><rights>Copyright © 2016 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-2c48642f468d19504207f7c333328e7e6ccbaaff443503a0afe2e894c5db6dfe3</citedby><cites>FETCH-LOGICAL-c474t-2c48642f468d19504207f7c333328e7e6ccbaaff443503a0afe2e894c5db6dfe3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0197458015005345$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26827642$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gispert, Juan Domingo</creatorcontrib><creatorcontrib>Monté, Gemma C</creatorcontrib><creatorcontrib>Falcon, Carles</creatorcontrib><creatorcontrib>Tucholka, Alan</creatorcontrib><creatorcontrib>Rojas, Santiago</creatorcontrib><creatorcontrib>Sánchez-Valle, Raquel</creatorcontrib><creatorcontrib>Antonell, Anna</creatorcontrib><creatorcontrib>Lladó, Albert</creatorcontrib><creatorcontrib>Rami, Lorena</creatorcontrib><creatorcontrib>Molinuevo, José Luis</creatorcontrib><title>CSF YKL-40 and pTau181 are related to different cerebral morphometric patterns in early AD</title><title>Neurobiology of aging</title><addtitle>Neurobiol Aging</addtitle><description>Abstract Cerebrospinal fluid (CSF) concentrations of YKL-40 that serve as biomarker of neuroinflammation are known to be altered along the clinico-biological continuum of Alzheimer's disease (AD). The specific structural cerebral correlates of CSF YKL-40 were evaluated across the early stages of AD from normal to preclinical to mild dementia. Nonlinear gray matter (GM) volume associations with CSF YKL-40 levels were assessed in a total of 116 subjects, including normal controls and those with preclinical AD as defined by CSF Aβ < 500 pg/mL, mild cognitive impairment (MCI) due to AD, or mild AD dementia. Age-corrected YKL-40 levels were increased in MCIs versus the rest of groups and showed an inverse u-shaped association with p-tau values. A similar nonlinear relationship was found between GM volume and YKL-40 in inferior and lateral temporal regions spreading to the supramarginal gyrus, insula, inferior frontal cortex, and cerebellum in MCI and AD. These findings for YKL-40 remained unchanged after adjusting for p-tau, which was found to be associated with GM volumes in distinct anatomic areas. CSF YKL-40, a biomarker of glial inflammation, is associated with a cerebral structural signature distinct from that related to p-tau neurodegeneration at the earliest stages of cognitive decline due to AD.</description><subject>Aged</subject><subject>Alzheimer Disease - diagnosis</subject><subject>Alzheimer Disease - pathology</subject><subject>Amyloid beta-Peptides - cerebrospinal fluid</subject><subject>Astrocyte</subject><subject>Astrocytes - pathology</subject><subject>Astrocytosis</subject><subject>Astroglia</subject><subject>Astrogliosis</subject><subject>Biomarkers - cerebrospinal fluid</subject><subject>Chitinase-3-Like Protein 1 - cerebrospinal fluid</subject><subject>Cognitive Dysfunction - diagnosis</subject><subject>Cognitive Dysfunction - pathology</subject><subject>Female</subject><subject>Glia</subject><subject>Gray Matter - pathology</subject><subject>Humans</subject><subject>Inflammation - diagnosis</subject><subject>Inflammation - pathology</subject><subject>Internal Medicine</subject><subject>Magnetic Resonance Imaging</subject><subject>Magnetic resonance imaging (MRI)</subject><subject>Male</subject><subject>Microglia</subject><subject>Microgliosis</subject><subject>Middle Aged</subject><subject>Neuroglia - pathology</subject><subject>Neuroimaging</subject><subject>Neuroinflammation</subject><subject>Neurology</subject><subject>Tau</subject><subject>tau Proteins - cerebrospinal fluid</subject><subject>Voxel-based morphometry (VBM)</subject><issn>0197-4580</issn><issn>1558-1497</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNUk2P0zAQtRCI7Rb-AvKBA5cU2_FXJYS0KnRBVOKwywEuluNMFpfEDnaC1H-Poy5IcNq5vMO8mTd6bxB6ScmGEipfHzcB5hQbH3t758PdhhEqSmtDGHuEVlQIXVG-VY_RitCtqrjQ5AJd5nwkhCiu5FN0waRmSnK2Qt92N3v89dOh4gTb0OLx1s5UU2wT4AS9naDFU8St7zpIECbsCjTJ9niIafweB5iSd3i00wQpZOwDBpv6E7569ww96Wyf4fk9rtGX_fvb3Yfq8Pn64-7qUDmu-FQxx3U5peNSt3QrCGdEdcrVpZgGBdK5xtqu47wWpLbEdsBAb7kTbSPbDuo1enXeO6b4c4Y8mcFnB31vA8Q5G6qkFkpLqR5CZaQmvGit0Zsz1aWYc4LOjMkPNp0MJWYJwhzNv0GYJYilW4Io4y_uleZmgPbv8B_nC2F_JkCx5peHZLLzEBy0PoGbTBv9Q5Xe_rfI9T54Z_sfcIJ8jHMKxX5DTWaGmJvlKZafoIIQUXNR_wY40bVf</recordid><startdate>20160201</startdate><enddate>20160201</enddate><creator>Gispert, Juan Domingo</creator><creator>Monté, Gemma C</creator><creator>Falcon, Carles</creator><creator>Tucholka, Alan</creator><creator>Rojas, Santiago</creator><creator>Sánchez-Valle, Raquel</creator><creator>Antonell, Anna</creator><creator>Lladó, Albert</creator><creator>Rami, Lorena</creator><creator>Molinuevo, José Luis</creator><general>Elsevier Inc</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>7X8</scope><scope>7TK</scope></search><sort><creationdate>20160201</creationdate><title>CSF YKL-40 and pTau181 are related to different cerebral morphometric patterns in early AD</title><author>Gispert, Juan Domingo ; Monté, Gemma C ; Falcon, Carles ; Tucholka, Alan ; Rojas, Santiago ; Sánchez-Valle, Raquel ; Antonell, Anna ; Lladó, Albert ; Rami, Lorena ; Molinuevo, José Luis</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-2c48642f468d19504207f7c333328e7e6ccbaaff443503a0afe2e894c5db6dfe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Aged</topic><topic>Alzheimer Disease - diagnosis</topic><topic>Alzheimer Disease - pathology</topic><topic>Amyloid beta-Peptides - cerebrospinal fluid</topic><topic>Astrocyte</topic><topic>Astrocytes - pathology</topic><topic>Astrocytosis</topic><topic>Astroglia</topic><topic>Astrogliosis</topic><topic>Biomarkers - cerebrospinal fluid</topic><topic>Chitinase-3-Like Protein 1 - cerebrospinal fluid</topic><topic>Cognitive Dysfunction - diagnosis</topic><topic>Cognitive Dysfunction - pathology</topic><topic>Female</topic><topic>Glia</topic><topic>Gray Matter - pathology</topic><topic>Humans</topic><topic>Inflammation - diagnosis</topic><topic>Inflammation - pathology</topic><topic>Internal Medicine</topic><topic>Magnetic Resonance Imaging</topic><topic>Magnetic resonance imaging (MRI)</topic><topic>Male</topic><topic>Microglia</topic><topic>Microgliosis</topic><topic>Middle Aged</topic><topic>Neuroglia - pathology</topic><topic>Neuroimaging</topic><topic>Neuroinflammation</topic><topic>Neurology</topic><topic>Tau</topic><topic>tau Proteins - cerebrospinal fluid</topic><topic>Voxel-based morphometry (VBM)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gispert, Juan Domingo</creatorcontrib><creatorcontrib>Monté, Gemma C</creatorcontrib><creatorcontrib>Falcon, Carles</creatorcontrib><creatorcontrib>Tucholka, Alan</creatorcontrib><creatorcontrib>Rojas, Santiago</creatorcontrib><creatorcontrib>Sánchez-Valle, Raquel</creatorcontrib><creatorcontrib>Antonell, Anna</creatorcontrib><creatorcontrib>Lladó, Albert</creatorcontrib><creatorcontrib>Rami, Lorena</creatorcontrib><creatorcontrib>Molinuevo, José Luis</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><jtitle>Neurobiology of aging</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gispert, Juan Domingo</au><au>Monté, Gemma C</au><au>Falcon, Carles</au><au>Tucholka, Alan</au><au>Rojas, Santiago</au><au>Sánchez-Valle, Raquel</au><au>Antonell, Anna</au><au>Lladó, Albert</au><au>Rami, Lorena</au><au>Molinuevo, José Luis</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CSF YKL-40 and pTau181 are related to different cerebral morphometric patterns in early AD</atitle><jtitle>Neurobiology of aging</jtitle><addtitle>Neurobiol Aging</addtitle><date>2016-02-01</date><risdate>2016</risdate><volume>38</volume><spage>47</spage><epage>55</epage><pages>47-55</pages><issn>0197-4580</issn><eissn>1558-1497</eissn><abstract>Abstract Cerebrospinal fluid (CSF) concentrations of YKL-40 that serve as biomarker of neuroinflammation are known to be altered along the clinico-biological continuum of Alzheimer's disease (AD). The specific structural cerebral correlates of CSF YKL-40 were evaluated across the early stages of AD from normal to preclinical to mild dementia. Nonlinear gray matter (GM) volume associations with CSF YKL-40 levels were assessed in a total of 116 subjects, including normal controls and those with preclinical AD as defined by CSF Aβ < 500 pg/mL, mild cognitive impairment (MCI) due to AD, or mild AD dementia. Age-corrected YKL-40 levels were increased in MCIs versus the rest of groups and showed an inverse u-shaped association with p-tau values. A similar nonlinear relationship was found between GM volume and YKL-40 in inferior and lateral temporal regions spreading to the supramarginal gyrus, insula, inferior frontal cortex, and cerebellum in MCI and AD. These findings for YKL-40 remained unchanged after adjusting for p-tau, which was found to be associated with GM volumes in distinct anatomic areas. CSF YKL-40, a biomarker of glial inflammation, is associated with a cerebral structural signature distinct from that related to p-tau neurodegeneration at the earliest stages of cognitive decline due to AD.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>26827642</pmid><doi>10.1016/j.neurobiolaging.2015.10.022</doi><tpages>9</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0197-4580 |
ispartof | Neurobiology of aging, 2016-02, Vol.38, p.47-55 |
issn | 0197-4580 1558-1497 |
language | eng |
recordid | cdi_proquest_miscellaneous_1768578667 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Aged Alzheimer Disease - diagnosis Alzheimer Disease - pathology Amyloid beta-Peptides - cerebrospinal fluid Astrocyte Astrocytes - pathology Astrocytosis Astroglia Astrogliosis Biomarkers - cerebrospinal fluid Chitinase-3-Like Protein 1 - cerebrospinal fluid Cognitive Dysfunction - diagnosis Cognitive Dysfunction - pathology Female Glia Gray Matter - pathology Humans Inflammation - diagnosis Inflammation - pathology Internal Medicine Magnetic Resonance Imaging Magnetic resonance imaging (MRI) Male Microglia Microgliosis Middle Aged Neuroglia - pathology Neuroimaging Neuroinflammation Neurology Tau tau Proteins - cerebrospinal fluid Voxel-based morphometry (VBM) |
title | CSF YKL-40 and pTau181 are related to different cerebral morphometric patterns in early AD |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-26T15%3A47%3A37IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=CSF%20YKL-40%20and%20pTau181%20are%20related%20to%20different%20cerebral%20morphometric%20patterns%20in%20early%20AD&rft.jtitle=Neurobiology%20of%20aging&rft.au=Gispert,%20Juan%20Domingo&rft.date=2016-02-01&rft.volume=38&rft.spage=47&rft.epage=55&rft.pages=47-55&rft.issn=0197-4580&rft.eissn=1558-1497&rft_id=info:doi/10.1016/j.neurobiolaging.2015.10.022&rft_dat=%3Cproquest_cross%3E1768578667%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1762030444&rft_id=info:pmid/26827642&rft_els_id=S0197458015005345&rfr_iscdi=true |