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Age-dependent inverse correlations in CSF and plasma amyloid-β(1–42) concentrations prior to amyloid plaque deposition in the brain of 3xTg-AD mice
Amyloid-β (Aβ) plays a critical role as a biomarker in Alzheimer’s disease (AD) diagnosis. In addition to its diagnostic potential in the brain, recent studies have suggested that changes of Aβ level in the plasma can possibly indicate AD onset. In this study, we found that plasma Aβ(1–42) concentra...
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Published in: | Scientific reports 2016-02, Vol.6 (1), p.20185-20185, Article 20185 |
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creator | Cho, Soo Min Lee, Sejin Yang, Seung-Hoon Kim, Hye Yun Lee, Michael Jisoo Kim, Hyunjin Vincent Kim, Jiyoon Baek, Seungyeop Yun, Jin Kim, Dohee Kim, Yun Kyung Cho, Yakdol Woo, Jiwan Kim, Tae Song Kim, YoungSoo |
description | Amyloid-β (Aβ) plays a critical role as a biomarker in Alzheimer’s disease (AD) diagnosis. In addition to its diagnostic potential in the brain, recent studies have suggested that changes of Aβ level in the plasma can possibly indicate AD onset. In this study, we found that plasma Aβ(1–42) concentration increases with age, while the concentration of Aβ(1–42) in the cerebrospinal fluid (CSF) decreases in APP
swe
, PS1
M146V
and Tau
P301L
transgenic (3xTg-AD) mice, if measurements were made before formation of ThS-positive plaques in the brain. Our data suggests that there is an inverse correlations between the plasma and CSF Aβ(1–42) levels until plaques form in transgenic mice’s brains and that the plasma Aβ concentration possesses the diagnostic potential as a biomarker for diagnosis of early AD stages. |
doi_str_mv | 10.1038/srep20185 |
format | article |
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swe
, PS1
M146V
and Tau
P301L
transgenic (3xTg-AD) mice, if measurements were made before formation of ThS-positive plaques in the brain. Our data suggests that there is an inverse correlations between the plasma and CSF Aβ(1–42) levels until plaques form in transgenic mice’s brains and that the plasma Aβ concentration possesses the diagnostic potential as a biomarker for diagnosis of early AD stages.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/srep20185</identifier><identifier>PMID: 26830653</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/378/1689/1283 ; 692/53/2421 ; 692/699/375/365/1283 ; 82 ; 82/51 ; Aging - blood ; Aging - cerebrospinal fluid ; Alzheimer Disease - blood ; Alzheimer Disease - cerebrospinal fluid ; Amyloid beta-Peptides - blood ; Amyloid beta-Peptides - cerebrospinal fluid ; Animals ; Blood-Brain Barrier - metabolism ; Brain - metabolism ; Female ; Humanities and Social Sciences ; Humans ; Immunohistochemistry ; Mice, Transgenic ; multidisciplinary ; Peptide Fragments - blood ; Peptide Fragments - cerebrospinal fluid ; Phosphorylation ; Plaque, Amyloid - blood ; Plaque, Amyloid - cerebrospinal fluid ; Protein Transport ; Science</subject><ispartof>Scientific reports, 2016-02, Vol.6 (1), p.20185-20185, Article 20185</ispartof><rights>The Author(s) 2016</rights><rights>Copyright © 2016, Macmillan Publishers Limited 2016 Macmillan Publishers Limited</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c410t-f0898d764fbbccce7e1180506388d6c3df7b080ba50a1c0d8236a2de6e8e75993</citedby><cites>FETCH-LOGICAL-c410t-f0898d764fbbccce7e1180506388d6c3df7b080ba50a1c0d8236a2de6e8e75993</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/PMC4735736/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4735736/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,37013,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26830653$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cho, Soo Min</creatorcontrib><creatorcontrib>Lee, Sejin</creatorcontrib><creatorcontrib>Yang, Seung-Hoon</creatorcontrib><creatorcontrib>Kim, Hye Yun</creatorcontrib><creatorcontrib>Lee, Michael Jisoo</creatorcontrib><creatorcontrib>Kim, Hyunjin Vincent</creatorcontrib><creatorcontrib>Kim, Jiyoon</creatorcontrib><creatorcontrib>Baek, Seungyeop</creatorcontrib><creatorcontrib>Yun, Jin</creatorcontrib><creatorcontrib>Kim, Dohee</creatorcontrib><creatorcontrib>Kim, Yun Kyung</creatorcontrib><creatorcontrib>Cho, Yakdol</creatorcontrib><creatorcontrib>Woo, Jiwan</creatorcontrib><creatorcontrib>Kim, Tae Song</creatorcontrib><creatorcontrib>Kim, YoungSoo</creatorcontrib><title>Age-dependent inverse correlations in CSF and plasma amyloid-β(1–42) concentrations prior to amyloid plaque deposition in the brain of 3xTg-AD mice</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Amyloid-β (Aβ) plays a critical role as a biomarker in Alzheimer’s disease (AD) diagnosis. In addition to its diagnostic potential in the brain, recent studies have suggested that changes of Aβ level in the plasma can possibly indicate AD onset. In this study, we found that plasma Aβ(1–42) concentration increases with age, while the concentration of Aβ(1–42) in the cerebrospinal fluid (CSF) decreases in APP
swe
, PS1
M146V
and Tau
P301L
transgenic (3xTg-AD) mice, if measurements were made before formation of ThS-positive plaques in the brain. Our data suggests that there is an inverse correlations between the plasma and CSF Aβ(1–42) levels until plaques form in transgenic mice’s brains and that the plasma Aβ concentration possesses the diagnostic potential as a biomarker for diagnosis of early AD stages.</description><subject>631/378/1689/1283</subject><subject>692/53/2421</subject><subject>692/699/375/365/1283</subject><subject>82</subject><subject>82/51</subject><subject>Aging - blood</subject><subject>Aging - cerebrospinal fluid</subject><subject>Alzheimer Disease - blood</subject><subject>Alzheimer Disease - cerebrospinal fluid</subject><subject>Amyloid beta-Peptides - blood</subject><subject>Amyloid beta-Peptides - cerebrospinal fluid</subject><subject>Animals</subject><subject>Blood-Brain Barrier - metabolism</subject><subject>Brain - metabolism</subject><subject>Female</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Mice, Transgenic</subject><subject>multidisciplinary</subject><subject>Peptide Fragments - blood</subject><subject>Peptide Fragments - cerebrospinal fluid</subject><subject>Phosphorylation</subject><subject>Plaque, Amyloid - blood</subject><subject>Plaque, Amyloid - cerebrospinal fluid</subject><subject>Protein Transport</subject><subject>Science</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNptkc9O3DAQxq0KVBBw6AtUPkKlgP8kjnNBWm1LQULiAJwtx54sRomd2llUbn2HSn2QPkgfok9Sr3ZZUQlfPPL85psZfwh9oOSUEi7PUoSRESqrd2ifkbIqGGds51W8h45SeiT5VKwpafMe7TEhOREV30e_ZgsoLIzgLfgJO_8EMQE2IUbo9eSCT_kRz28vsPYWj71Og8Z6eO6Ds8Wf38f074-fJTvJFd5khbipGaMLEU_hBV1VflsCzq1CcitmJTs9AG6jzlHoMP9-tyhmn_HgDByi3U73CY429wG6v_hyN78srm--Xs1n14UpKZmKjshG2lqUXdsaY6AGSiWpiOBSWmG47eqWSNLqimhqiJWMC80sCJBQV03DD9D5WndctgPY9Qa9ytMPOj6roJ36P-Pdg1qEJ1XWvKq5yALHG4EY8n5pUoNLBvpeewjLpGgtGC9LKmlGT9aoiSFl17ptG0rUykq1tTKzH1_PtSVfjMvApzWQcsovIKrHsIw-_9Ubav8AgpCsBw</recordid><startdate>20160202</startdate><enddate>20160202</enddate><creator>Cho, Soo Min</creator><creator>Lee, Sejin</creator><creator>Yang, Seung-Hoon</creator><creator>Kim, Hye Yun</creator><creator>Lee, Michael Jisoo</creator><creator>Kim, Hyunjin Vincent</creator><creator>Kim, Jiyoon</creator><creator>Baek, Seungyeop</creator><creator>Yun, Jin</creator><creator>Kim, Dohee</creator><creator>Kim, Yun Kyung</creator><creator>Cho, Yakdol</creator><creator>Woo, Jiwan</creator><creator>Kim, Tae Song</creator><creator>Kim, YoungSoo</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160202</creationdate><title>Age-dependent inverse correlations in CSF and plasma amyloid-β(1–42) concentrations prior to amyloid plaque deposition in the brain of 3xTg-AD mice</title><author>Cho, Soo Min ; Lee, Sejin ; Yang, Seung-Hoon ; Kim, Hye Yun ; Lee, Michael Jisoo ; Kim, Hyunjin Vincent ; Kim, Jiyoon ; Baek, Seungyeop ; Yun, Jin ; Kim, Dohee ; Kim, Yun Kyung ; Cho, Yakdol ; Woo, Jiwan ; Kim, Tae Song ; Kim, YoungSoo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c410t-f0898d764fbbccce7e1180506388d6c3df7b080ba50a1c0d8236a2de6e8e75993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>631/378/1689/1283</topic><topic>692/53/2421</topic><topic>692/699/375/365/1283</topic><topic>82</topic><topic>82/51</topic><topic>Aging - blood</topic><topic>Aging - cerebrospinal fluid</topic><topic>Alzheimer Disease - blood</topic><topic>Alzheimer Disease - cerebrospinal fluid</topic><topic>Amyloid beta-Peptides - blood</topic><topic>Amyloid beta-Peptides - cerebrospinal fluid</topic><topic>Animals</topic><topic>Blood-Brain Barrier - metabolism</topic><topic>Brain - metabolism</topic><topic>Female</topic><topic>Humanities and Social Sciences</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Mice, Transgenic</topic><topic>multidisciplinary</topic><topic>Peptide Fragments - blood</topic><topic>Peptide Fragments - cerebrospinal fluid</topic><topic>Phosphorylation</topic><topic>Plaque, Amyloid - blood</topic><topic>Plaque, Amyloid - cerebrospinal fluid</topic><topic>Protein Transport</topic><topic>Science</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cho, Soo Min</creatorcontrib><creatorcontrib>Lee, Sejin</creatorcontrib><creatorcontrib>Yang, Seung-Hoon</creatorcontrib><creatorcontrib>Kim, Hye Yun</creatorcontrib><creatorcontrib>Lee, Michael Jisoo</creatorcontrib><creatorcontrib>Kim, Hyunjin Vincent</creatorcontrib><creatorcontrib>Kim, Jiyoon</creatorcontrib><creatorcontrib>Baek, Seungyeop</creatorcontrib><creatorcontrib>Yun, Jin</creatorcontrib><creatorcontrib>Kim, Dohee</creatorcontrib><creatorcontrib>Kim, Yun Kyung</creatorcontrib><creatorcontrib>Cho, Yakdol</creatorcontrib><creatorcontrib>Woo, Jiwan</creatorcontrib><creatorcontrib>Kim, Tae Song</creatorcontrib><creatorcontrib>Kim, YoungSoo</creatorcontrib><collection>SpringerOpen</collection><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>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cho, Soo Min</au><au>Lee, Sejin</au><au>Yang, Seung-Hoon</au><au>Kim, Hye Yun</au><au>Lee, Michael Jisoo</au><au>Kim, Hyunjin Vincent</au><au>Kim, Jiyoon</au><au>Baek, Seungyeop</au><au>Yun, Jin</au><au>Kim, Dohee</au><au>Kim, Yun Kyung</au><au>Cho, Yakdol</au><au>Woo, Jiwan</au><au>Kim, Tae Song</au><au>Kim, YoungSoo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Age-dependent inverse correlations in CSF and plasma amyloid-β(1–42) concentrations prior to amyloid plaque deposition in the brain of 3xTg-AD mice</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2016-02-02</date><risdate>2016</risdate><volume>6</volume><issue>1</issue><spage>20185</spage><epage>20185</epage><pages>20185-20185</pages><artnum>20185</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Amyloid-β (Aβ) plays a critical role as a biomarker in Alzheimer’s disease (AD) diagnosis. In addition to its diagnostic potential in the brain, recent studies have suggested that changes of Aβ level in the plasma can possibly indicate AD onset. In this study, we found that plasma Aβ(1–42) concentration increases with age, while the concentration of Aβ(1–42) in the cerebrospinal fluid (CSF) decreases in APP
swe
, PS1
M146V
and Tau
P301L
transgenic (3xTg-AD) mice, if measurements were made before formation of ThS-positive plaques in the brain. Our data suggests that there is an inverse correlations between the plasma and CSF Aβ(1–42) levels until plaques form in transgenic mice’s brains and that the plasma Aβ concentration possesses the diagnostic potential as a biomarker for diagnosis of early AD stages.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>26830653</pmid><doi>10.1038/srep20185</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 631/378/1689/1283 692/53/2421 692/699/375/365/1283 82 82/51 Aging - blood Aging - cerebrospinal fluid Alzheimer Disease - blood Alzheimer Disease - cerebrospinal fluid Amyloid beta-Peptides - blood Amyloid beta-Peptides - cerebrospinal fluid Animals Blood-Brain Barrier - metabolism Brain - metabolism Female Humanities and Social Sciences Humans Immunohistochemistry Mice, Transgenic multidisciplinary Peptide Fragments - blood Peptide Fragments - cerebrospinal fluid Phosphorylation Plaque, Amyloid - blood Plaque, Amyloid - cerebrospinal fluid Protein Transport Science |
title | Age-dependent inverse correlations in CSF and plasma amyloid-β(1–42) concentrations prior to amyloid plaque deposition in the brain of 3xTg-AD mice |
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