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 |
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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. |
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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.</description><identifier>ISSN: 1948-7193</identifier><identifier>EISSN: 1948-7193</identifier><identifier>DOI: 10.1021/cn400129p</identifier><identifier>PMID: 24090201</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>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</subject><ispartof>ACS chemical neuroscience, 2013-12, Vol.4 (12), p.1530-1536</ispartof><rights>Copyright © 2013 American Chemical Society</rights><rights>Copyright © 2013 American Chemical Society 2013 American Chemical Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a445t-12ad4e0c532177ee697410555e73ad231cbc54ab6f1e2b4bfcb9074845d48c2d3</citedby><cites>FETCH-LOGICAL-a445t-12ad4e0c532177ee697410555e73ad231cbc54ab6f1e2b4bfcb9074845d48c2d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/cn400129p$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/cn400129p$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,2752,27053,27901,27902,53766,53768,56713,56763</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24090201$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><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><title>Combined Plasma Biomarkers for Diagnosing Mild Cognition Impairment and Alzheimer’s Disease</title><title>ACS chemical neuroscience</title><addtitle>ACS Chem. 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. 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.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Alzheimer Disease - blood</subject><subject>Alzheimer Disease - diagnosis</subject><subject>Amyloid beta-Peptides - blood</subject><subject>Biomarkers - blood</subject><subject>Cognitive Dysfunction - blood</subject><subject>Cognitive Dysfunction - diagnosis</subject><subject>Female</subject><subject>Humans</subject><subject>Immunoassay - methods</subject><subject>Male</subject><subject>Middle Aged</subject><subject>tau Proteins - blood</subject><subject>Young Adult</subject><issn>1948-7193</issn><issn>1948-7193</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkc1KAzEQx4MoWj8OvoDkIuihmmSz2c1F0PpVqOhBjxKy2dmaupvUpBX05Gv4ej6JK62lgqcZmN_85z8zCO1SckQJo8fGcUIok-MV1KGS592MymR1Kd9AmzGOCBGS5GIdbTBOJGGEdtBjzzeFdVDiu1rHRuMz6xsdniFEXPmAz60eOh-tG-IbW5e454fOTqx3uN-MtQ0NuAnWrsSn9fsT2AbC18dnbNsi6AjbaK3SdYSdedxCD5cX973r7uD2qt87HXQ15-mkS5kuORCTJoxmGYCQGackTVPIEl2yhJrCpFwXoqLACl5UppAk4zlPS54bViZb6GSmO54WDZSmNRV0rcbBtru8Ka-t-ltx9kkN_atKcpFJIVqBg7lA8C9TiBPV2GigrrUDP42KciFFIplgLXo4Q03wMQaoFmMoUT_vUIt3tOzesq8F-Xv_FtifAdpENfLT4Noz_SP0DWxmk60</recordid><startdate>20131218</startdate><enddate>20131218</enddate><creator>Chiu, Ming-Jang</creator><creator>Yang, Shieh-Yueh</creator><creator>Horng, Herng-Er</creator><creator>Yang, Che-Chuan</creator><creator>Chen, Ta-Fu</creator><creator>Chieh, Jen-Je</creator><creator>Chen, Hsin-Hsien</creator><creator>Chen, Ting-Chi</creator><creator>Ho, Chia-Shin</creator><creator>Chang, Shuo-Fen</creator><creator>Liu, Hao Chun</creator><creator>Hong, Chin-Yih</creator><creator>Yang, Hong-Chang</creator><general>American Chemical Society</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>5PM</scope></search><sort><creationdate>20131218</creationdate><title>Combined Plasma Biomarkers for Diagnosing Mild Cognition Impairment and Alzheimer’s Disease</title><author>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</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. Neurosci</addtitle><date>2013-12-18</date><risdate>2013</risdate><volume>4</volume><issue>12</issue><spage>1530</spage><epage>1536</epage><pages>1530-1536</pages><issn>1948-7193</issn><eissn>1948-7193</eissn><abstract>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.</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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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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