Stability of CSF beta-amyloid(1-42) and tau levels by APOE genotype in Alzheimer patients
Cerebrospinal fluid (CSF) measures of beta-amyloid(1-42 )and tau differ between patients with Alzheimer's Disease (AD) and elderly normal controls. The effect of time and APOE genotype on these biomarkers continues to be elucidated. We assessed CSF beta-amyloid(1-42) and tau in 20 mild-to-moder...
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Veröffentlicht in: | Dementia and geriatric cognitive disorders 2006, Vol.22 (1), p.48-53 |
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creator | Huey, Edward D Mirza, Nadeem Putnam, Karen T Soares, Holly Csako, Gyorgy Levy, James A Copenhaver, Brittany Cohen, Robert M Sunderland, Trey |
description | Cerebrospinal fluid (CSF) measures of beta-amyloid(1-42 )and tau differ between patients with Alzheimer's Disease (AD) and elderly normal controls. The effect of time and APOE genotype on these biomarkers continues to be elucidated.
We assessed CSF beta-amyloid(1-42) and tau in 20 mild-to-moderate AD patients, 11 APOE epsilon4+ and 9 APOE epsilon4-, over a mean time of 3.8 years (range 1-11.1 years).
Over the period measured, CSF beta-amyloid(1-42) levels were lower in APOE epsilon4+ compared to APOE epsilon4- patients, and the levels decreased over time. Tau levels were stable over time and did not show an effect of APOE allele.
While this is a limited clinical sample, the further decrease in CSF beta-amyloid(1-42 )(i.e., more abnormal) combined with the CSF tau stability over a mean period of almost 4 years suggests that beta-amyloid(1-42 )and tau maintain their potential usefulness as diagnostic biomarkers over time. These findings should be taken into account if CSF beta-amyloid(1-42) and tau are used as measures of treatment response. |
doi_str_mv | 10.1159/000093261 |
format | Article |
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We assessed CSF beta-amyloid(1-42) and tau in 20 mild-to-moderate AD patients, 11 APOE epsilon4+ and 9 APOE epsilon4-, over a mean time of 3.8 years (range 1-11.1 years).
Over the period measured, CSF beta-amyloid(1-42) levels were lower in APOE epsilon4+ compared to APOE epsilon4- patients, and the levels decreased over time. Tau levels were stable over time and did not show an effect of APOE allele.
While this is a limited clinical sample, the further decrease in CSF beta-amyloid(1-42 )(i.e., more abnormal) combined with the CSF tau stability over a mean period of almost 4 years suggests that beta-amyloid(1-42 )and tau maintain their potential usefulness as diagnostic biomarkers over time. These findings should be taken into account if CSF beta-amyloid(1-42) and tau are used as measures of treatment response.</description><identifier>ISSN: 1420-8008</identifier><identifier>DOI: 10.1159/000093261</identifier><identifier>PMID: 16682793</identifier><language>eng</language><publisher>Switzerland</publisher><subject>Aged ; Alleles ; Alzheimer Disease - cerebrospinal fluid ; Alzheimer Disease - genetics ; Amyloid beta-Peptides - cerebrospinal fluid ; Apolipoproteins E - genetics ; Biomarkers ; Female ; Genotype ; Humans ; Male ; Middle Aged ; Neuropsychological Tests ; Peptide Fragments - cerebrospinal fluid ; tau Proteins - cerebrospinal fluid</subject><ispartof>Dementia and geriatric cognitive disorders, 2006, Vol.22 (1), p.48-53</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4009,27902,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16682793$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Huey, Edward D</creatorcontrib><creatorcontrib>Mirza, Nadeem</creatorcontrib><creatorcontrib>Putnam, Karen T</creatorcontrib><creatorcontrib>Soares, Holly</creatorcontrib><creatorcontrib>Csako, Gyorgy</creatorcontrib><creatorcontrib>Levy, James A</creatorcontrib><creatorcontrib>Copenhaver, Brittany</creatorcontrib><creatorcontrib>Cohen, Robert M</creatorcontrib><creatorcontrib>Sunderland, Trey</creatorcontrib><title>Stability of CSF beta-amyloid(1-42) and tau levels by APOE genotype in Alzheimer patients</title><title>Dementia and geriatric cognitive disorders</title><addtitle>Dement Geriatr Cogn Disord</addtitle><description>Cerebrospinal fluid (CSF) measures of beta-amyloid(1-42 )and tau differ between patients with Alzheimer's Disease (AD) and elderly normal controls. The effect of time and APOE genotype on these biomarkers continues to be elucidated.
We assessed CSF beta-amyloid(1-42) and tau in 20 mild-to-moderate AD patients, 11 APOE epsilon4+ and 9 APOE epsilon4-, over a mean time of 3.8 years (range 1-11.1 years).
Over the period measured, CSF beta-amyloid(1-42) levels were lower in APOE epsilon4+ compared to APOE epsilon4- patients, and the levels decreased over time. Tau levels were stable over time and did not show an effect of APOE allele.
While this is a limited clinical sample, the further decrease in CSF beta-amyloid(1-42 )(i.e., more abnormal) combined with the CSF tau stability over a mean period of almost 4 years suggests that beta-amyloid(1-42 )and tau maintain their potential usefulness as diagnostic biomarkers over time. These findings should be taken into account if CSF beta-amyloid(1-42) and tau are used as measures of treatment response.</description><subject>Aged</subject><subject>Alleles</subject><subject>Alzheimer Disease - cerebrospinal fluid</subject><subject>Alzheimer Disease - genetics</subject><subject>Amyloid beta-Peptides - cerebrospinal fluid</subject><subject>Apolipoproteins E - genetics</subject><subject>Biomarkers</subject><subject>Female</subject><subject>Genotype</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neuropsychological Tests</subject><subject>Peptide Fragments - cerebrospinal fluid</subject><subject>tau Proteins - cerebrospinal fluid</subject><issn>1420-8008</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kDtPwzAYRT2AaCkM_AHkCcEQ8CPxY6yqFpAqFakwMEVO_AWMnAexUyn8eiJR7nKGe3SHi9AVJfeUZvqBTNGcCXqC5jRlJFGEqBk6D-FramQm9BmaUSEUk5rP0fs-msJ5F0fcVni13-ACoklMPfrW2VuapOwOm8biaAbs4QA-4GLEy5fdGn9A08axA-wavPQ_n-Bq6HFnooMmhgt0Whkf4PLIBXrbrF9XT8l29_i8Wm6TjnIdEw4CmGZVmVpdKSDcaAnc6pJYK4Exog1XZSVtWmqtTMFkUUoQVIEmNssEX6Cbv92ub78HCDGvXSjBe9NAO4RcKKKo5GoSr4_iUNRg8653tenH_P8M_gvojlyb</recordid><startdate>2006</startdate><enddate>2006</enddate><creator>Huey, Edward D</creator><creator>Mirza, Nadeem</creator><creator>Putnam, Karen T</creator><creator>Soares, Holly</creator><creator>Csako, Gyorgy</creator><creator>Levy, James A</creator><creator>Copenhaver, Brittany</creator><creator>Cohen, Robert M</creator><creator>Sunderland, Trey</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>2006</creationdate><title>Stability of CSF beta-amyloid(1-42) and tau levels by APOE genotype in Alzheimer patients</title><author>Huey, Edward D ; Mirza, Nadeem ; Putnam, Karen T ; Soares, Holly ; Csako, Gyorgy ; Levy, James A ; Copenhaver, Brittany ; Cohen, Robert M ; Sunderland, Trey</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p139t-3e6e292fc4d9f8e03a97e3d9c0dd7e2209a38cf7d4c998ab27bc7e618e90d5563</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Aged</topic><topic>Alleles</topic><topic>Alzheimer Disease - cerebrospinal fluid</topic><topic>Alzheimer Disease - genetics</topic><topic>Amyloid beta-Peptides - cerebrospinal fluid</topic><topic>Apolipoproteins E - genetics</topic><topic>Biomarkers</topic><topic>Female</topic><topic>Genotype</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neuropsychological Tests</topic><topic>Peptide Fragments - cerebrospinal fluid</topic><topic>tau Proteins - cerebrospinal fluid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huey, Edward D</creatorcontrib><creatorcontrib>Mirza, Nadeem</creatorcontrib><creatorcontrib>Putnam, Karen T</creatorcontrib><creatorcontrib>Soares, Holly</creatorcontrib><creatorcontrib>Csako, Gyorgy</creatorcontrib><creatorcontrib>Levy, James A</creatorcontrib><creatorcontrib>Copenhaver, Brittany</creatorcontrib><creatorcontrib>Cohen, Robert M</creatorcontrib><creatorcontrib>Sunderland, Trey</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Dementia and geriatric cognitive disorders</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huey, Edward D</au><au>Mirza, Nadeem</au><au>Putnam, Karen T</au><au>Soares, Holly</au><au>Csako, Gyorgy</au><au>Levy, James A</au><au>Copenhaver, Brittany</au><au>Cohen, Robert M</au><au>Sunderland, Trey</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stability of CSF beta-amyloid(1-42) and tau levels by APOE genotype in Alzheimer patients</atitle><jtitle>Dementia and geriatric cognitive disorders</jtitle><addtitle>Dement Geriatr Cogn Disord</addtitle><date>2006</date><risdate>2006</risdate><volume>22</volume><issue>1</issue><spage>48</spage><epage>53</epage><pages>48-53</pages><issn>1420-8008</issn><abstract>Cerebrospinal fluid (CSF) measures of beta-amyloid(1-42 )and tau differ between patients with Alzheimer's Disease (AD) and elderly normal controls. The effect of time and APOE genotype on these biomarkers continues to be elucidated.
We assessed CSF beta-amyloid(1-42) and tau in 20 mild-to-moderate AD patients, 11 APOE epsilon4+ and 9 APOE epsilon4-, over a mean time of 3.8 years (range 1-11.1 years).
Over the period measured, CSF beta-amyloid(1-42) levels were lower in APOE epsilon4+ compared to APOE epsilon4- patients, and the levels decreased over time. Tau levels were stable over time and did not show an effect of APOE allele.
While this is a limited clinical sample, the further decrease in CSF beta-amyloid(1-42 )(i.e., more abnormal) combined with the CSF tau stability over a mean period of almost 4 years suggests that beta-amyloid(1-42 )and tau maintain their potential usefulness as diagnostic biomarkers over time. These findings should be taken into account if CSF beta-amyloid(1-42) and tau are used as measures of treatment response.</abstract><cop>Switzerland</cop><pmid>16682793</pmid><doi>10.1159/000093261</doi><tpages>6</tpages></addata></record> |
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subjects | Aged Alleles Alzheimer Disease - cerebrospinal fluid Alzheimer Disease - genetics Amyloid beta-Peptides - cerebrospinal fluid Apolipoproteins E - genetics Biomarkers Female Genotype Humans Male Middle Aged Neuropsychological Tests Peptide Fragments - cerebrospinal fluid tau Proteins - cerebrospinal fluid |
title | Stability of CSF beta-amyloid(1-42) and tau levels by APOE genotype in Alzheimer patients |
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