Combined Plasma Biomarkers for Diagnosing Mild Cognition Impairment and Alzheimer’s Disease

A highly sensitive immunoassay, the immunomagnetic reduction, is used to measure several biomarkers for plasma that is related to Alzheimer’s disease (AD). These biomarkers include Aβ-40, Aβ-42, and tau proteins. The samples are composed of four groups: healthy controls (n = 66), mild cognitive impa...

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Veröffentlicht in:ACS chemical neuroscience 2013-12, Vol.4 (12), p.1530-1536
Hauptverfasser: Chiu, Ming-Jang, Yang, Shieh-Yueh, Horng, Herng-Er, Yang, Che-Chuan, Chen, Ta-Fu, Chieh, Jen-Je, Chen, Hsin-Hsien, Chen, Ting-Chi, Ho, Chia-Shin, Chang, Shuo-Fen, Liu, Hao Chun, Hong, Chin-Yih, Yang, Hong-Chang
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container_issue 12
container_start_page 1530
container_title ACS chemical neuroscience
container_volume 4
creator Chiu, Ming-Jang
Yang, Shieh-Yueh
Horng, Herng-Er
Yang, Che-Chuan
Chen, Ta-Fu
Chieh, Jen-Je
Chen, Hsin-Hsien
Chen, Ting-Chi
Ho, Chia-Shin
Chang, Shuo-Fen
Liu, Hao Chun
Hong, Chin-Yih
Yang, Hong-Chang
description A highly sensitive immunoassay, the immunomagnetic reduction, is used to measure several biomarkers for plasma that is related to Alzheimer’s disease (AD). These biomarkers include Aβ-40, Aβ-42, and tau proteins. The samples are composed of four groups: healthy controls (n = 66), mild cognitive impairment (MCI, n = 22), very mild dementia (n = 23), and mild-to-serve dementia, all due to AD (n = 22). It is found that the concentrations of both Aβ-42 and tau protein for the healthy controls are significantly lower than those of all of the other groups. The sensitivity and the specificity of plasma Aβ-42 and tau protein in differentiating MCI from AD are all around 0.9 (0.88–0.97). However, neither plasma Aβ-42 nor tau-protein concentration is an adequate parameter to distinguish MCI from AD. A parameter is proposed, which is the product of plasma Aβ-42 and tau-protein levels, to differentiate MCI from AD. The sensitivity and specificity are found to be 0.80 and 0.82, respectively. It is concluded that the use of combined plasma biomarkers not only allows the differentiation of the healthy controls and patients with AD in both the prodromal phase and the dementia phase, but it also allows AD in the prodromal phase to be distinguished from that in the dementia phase.
doi_str_mv 10.1021/cn400129p
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Neurosci</addtitle><description>A highly sensitive immunoassay, the immunomagnetic reduction, is used to measure several biomarkers for plasma that is related to Alzheimer’s disease (AD). These biomarkers include Aβ-40, Aβ-42, and tau proteins. The samples are composed of four groups: healthy controls (n = 66), mild cognitive impairment (MCI, n = 22), very mild dementia (n = 23), and mild-to-serve dementia, all due to AD (n = 22). It is found that the concentrations of both Aβ-42 and tau protein for the healthy controls are significantly lower than those of all of the other groups. The sensitivity and the specificity of plasma Aβ-42 and tau protein in differentiating MCI from AD are all around 0.9 (0.88–0.97). However, neither plasma Aβ-42 nor tau-protein concentration is an adequate parameter to distinguish MCI from AD. A parameter is proposed, which is the product of plasma Aβ-42 and tau-protein levels, to differentiate MCI from AD. The sensitivity and specificity are found to be 0.80 and 0.82, respectively. 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Yang, Shieh-Yueh ; Horng, Herng-Er ; Yang, Che-Chuan ; Chen, Ta-Fu ; Chieh, Jen-Je ; Chen, Hsin-Hsien ; Chen, Ting-Chi ; Ho, Chia-Shin ; Chang, Shuo-Fen ; Liu, Hao Chun ; Hong, Chin-Yih ; Yang, Hong-Chang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a445t-12ad4e0c532177ee697410555e73ad231cbc54ab6f1e2b4bfcb9074845d48c2d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Alzheimer Disease - blood</topic><topic>Alzheimer Disease - diagnosis</topic><topic>Amyloid beta-Peptides - blood</topic><topic>Biomarkers - blood</topic><topic>Cognitive Dysfunction - blood</topic><topic>Cognitive Dysfunction - diagnosis</topic><topic>Female</topic><topic>Humans</topic><topic>Immunoassay - methods</topic><topic>Male</topic><topic>Middle Aged</topic><topic>tau Proteins - blood</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chiu, Ming-Jang</creatorcontrib><creatorcontrib>Yang, Shieh-Yueh</creatorcontrib><creatorcontrib>Horng, Herng-Er</creatorcontrib><creatorcontrib>Yang, Che-Chuan</creatorcontrib><creatorcontrib>Chen, Ta-Fu</creatorcontrib><creatorcontrib>Chieh, Jen-Je</creatorcontrib><creatorcontrib>Chen, Hsin-Hsien</creatorcontrib><creatorcontrib>Chen, Ting-Chi</creatorcontrib><creatorcontrib>Ho, Chia-Shin</creatorcontrib><creatorcontrib>Chang, Shuo-Fen</creatorcontrib><creatorcontrib>Liu, Hao Chun</creatorcontrib><creatorcontrib>Hong, Chin-Yih</creatorcontrib><creatorcontrib>Yang, Hong-Chang</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>PubMed Central (Full Participant titles)</collection><jtitle>ACS chemical neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chiu, Ming-Jang</au><au>Yang, Shieh-Yueh</au><au>Horng, Herng-Er</au><au>Yang, Che-Chuan</au><au>Chen, Ta-Fu</au><au>Chieh, Jen-Je</au><au>Chen, Hsin-Hsien</au><au>Chen, Ting-Chi</au><au>Ho, Chia-Shin</au><au>Chang, Shuo-Fen</au><au>Liu, Hao Chun</au><au>Hong, Chin-Yih</au><au>Yang, Hong-Chang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Combined Plasma Biomarkers for Diagnosing Mild Cognition Impairment and Alzheimer’s Disease</atitle><jtitle>ACS chemical neuroscience</jtitle><addtitle>ACS Chem. 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However, neither plasma Aβ-42 nor tau-protein concentration is an adequate parameter to distinguish MCI from AD. A parameter is proposed, which is the product of plasma Aβ-42 and tau-protein levels, to differentiate MCI from AD. The sensitivity and specificity are found to be 0.80 and 0.82, respectively. It is concluded that the use of combined plasma biomarkers not only allows the differentiation of the healthy controls and patients with AD in both the prodromal phase and the dementia phase, but it also allows AD in the prodromal phase to be distinguished from that in the dementia phase.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>24090201</pmid><doi>10.1021/cn400129p</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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source ACS Publications; MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
subjects Adult
Aged
Aged, 80 and over
Alzheimer Disease - blood
Alzheimer Disease - diagnosis
Amyloid beta-Peptides - blood
Biomarkers - blood
Cognitive Dysfunction - blood
Cognitive Dysfunction - diagnosis
Female
Humans
Immunoassay - methods
Male
Middle Aged
tau Proteins - blood
Young Adult
title Combined Plasma Biomarkers for Diagnosing Mild Cognition Impairment and Alzheimer’s Disease
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