Elevation of plasma soluble amyloid precursor protein beta in Alzheimer’s disease

•Plasma sAPPβ levels is higher in Alzheimer’s disease patients than in controls.•Plasma sAPPβ levels tends to increase with increasing cognitive impairment.•sAPPα and sAPPβ in plasma have a strong positive correlation, which is stronger in MCI and AD than in controls. Beta-amyloid is considered to b...

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Veröffentlicht in:Archives of gerontology and geriatrics 2020-03, Vol.87, p.103995-103995, Article 103995
Hauptverfasser: Yun, Sang-Moon, Cho, Sun-Jung, Jo, Chulman, Park, Moon Ho, Han, Changsu, Koh, Young Ho
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container_title Archives of gerontology and geriatrics
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creator Yun, Sang-Moon
Cho, Sun-Jung
Jo, Chulman
Park, Moon Ho
Han, Changsu
Koh, Young Ho
description •Plasma sAPPβ levels is higher in Alzheimer’s disease patients than in controls.•Plasma sAPPβ levels tends to increase with increasing cognitive impairment.•sAPPα and sAPPβ in plasma have a strong positive correlation, which is stronger in MCI and AD than in controls. Beta-amyloid is considered to be a pathophysiological marker in Alzheimer's disease (AD). Soluble amyloid precursor proteins (sAPPs) –α (sAPPα) and –β (sAPPβ), which are the byproducts of non-amyloidogenic and amyloidogenic process of APP, respectively, have been repeatedly observed in the cerebrospinal fluids (CSF) of AD patients. The present study focused on the determination of sAPP levels in peripheral blood. The plasma protein levels of sAPPα and sAPPβ were measured with ELISA. Plasma from 52 AD patients, 98 amnestic mild cognitive impairment (MCI) patients, and 114 cognitively normal controls were compared. The plasma level of sAPPβ was significantly increased in AD patients than in cognitively healthy controls. However, no significant change in plasma sAPPα was observed among the three groups. Furthermore, the plasma sAPPβ levels significantly correlated with cognitive assessment scales, such as clinical dementia rating (CDR), and mini-mental status examination (MMSE). Interestingly, sAPPα and sAPPβ had a positive correlation with each other in blood plasma, similar to previous studies on CSF sAPP. This correlation was stronger in the MCI and AD groups than in the cognitively healthy controls. These results suggest that individuals with elevated plasma sAPPβ levels are at an increased risk of AD; elevation in these levels may reflect the progression of disease.
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Beta-amyloid is considered to be a pathophysiological marker in Alzheimer's disease (AD). Soluble amyloid precursor proteins (sAPPs) –α (sAPPα) and –β (sAPPβ), which are the byproducts of non-amyloidogenic and amyloidogenic process of APP, respectively, have been repeatedly observed in the cerebrospinal fluids (CSF) of AD patients. The present study focused on the determination of sAPP levels in peripheral blood. The plasma protein levels of sAPPα and sAPPβ were measured with ELISA. Plasma from 52 AD patients, 98 amnestic mild cognitive impairment (MCI) patients, and 114 cognitively normal controls were compared. The plasma level of sAPPβ was significantly increased in AD patients than in cognitively healthy controls. However, no significant change in plasma sAPPα was observed among the three groups. Furthermore, the plasma sAPPβ levels significantly correlated with cognitive assessment scales, such as clinical dementia rating (CDR), and mini-mental status examination (MMSE). Interestingly, sAPPα and sAPPβ had a positive correlation with each other in blood plasma, similar to previous studies on CSF sAPP. This correlation was stronger in the MCI and AD groups than in the cognitively healthy controls. These results suggest that individuals with elevated plasma sAPPβ levels are at an increased risk of AD; elevation in these levels may reflect the progression of disease.</description><identifier>ISSN: 0167-4943</identifier><identifier>EISSN: 1872-6976</identifier><identifier>DOI: 10.1016/j.archger.2019.103995</identifier><identifier>PMID: 31874328</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Alzheimer’s disease (AD) ; Cognitive impairment ; Plasma biomarker ; Soluble amyloid precursor proteins alpha (sAPPα) ; Soluble amyloid precursor proteins beta (sAPPβ)</subject><ispartof>Archives of gerontology and geriatrics, 2020-03, Vol.87, p.103995-103995, Article 103995</ispartof><rights>2019 Elsevier B.V.</rights><rights>Copyright © 2019 Elsevier B.V. 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Beta-amyloid is considered to be a pathophysiological marker in Alzheimer's disease (AD). Soluble amyloid precursor proteins (sAPPs) –α (sAPPα) and –β (sAPPβ), which are the byproducts of non-amyloidogenic and amyloidogenic process of APP, respectively, have been repeatedly observed in the cerebrospinal fluids (CSF) of AD patients. The present study focused on the determination of sAPP levels in peripheral blood. The plasma protein levels of sAPPα and sAPPβ were measured with ELISA. Plasma from 52 AD patients, 98 amnestic mild cognitive impairment (MCI) patients, and 114 cognitively normal controls were compared. The plasma level of sAPPβ was significantly increased in AD patients than in cognitively healthy controls. However, no significant change in plasma sAPPα was observed among the three groups. Furthermore, the plasma sAPPβ levels significantly correlated with cognitive assessment scales, such as clinical dementia rating (CDR), and mini-mental status examination (MMSE). Interestingly, sAPPα and sAPPβ had a positive correlation with each other in blood plasma, similar to previous studies on CSF sAPP. This correlation was stronger in the MCI and AD groups than in the cognitively healthy controls. These results suggest that individuals with elevated plasma sAPPβ levels are at an increased risk of AD; elevation in these levels may reflect the progression of disease.</description><subject>Alzheimer’s disease (AD)</subject><subject>Cognitive impairment</subject><subject>Plasma biomarker</subject><subject>Soluble amyloid precursor proteins alpha (sAPPα)</subject><subject>Soluble amyloid precursor proteins beta (sAPPβ)</subject><issn>0167-4943</issn><issn>1872-6976</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFkEtOwzAQhi0EoqVwBFCWbFL8yMsrVFXlIVViAawtx5lQV05c7KRSWXENrsdJcJXCltVYo-_3zHwIXRI8JZhkN-updGr1Bm5KMeGhxzhPj9CYFDmNM55nx2gcuDxOeMJG6Mz7NcY4wTQ7RSMWqITRYoyeFwa2stO2jWwdbYz0jYy8NX1pIJLNzlhdRRsHqnfeuvCyHeg2KqGTUagz87EC3YD7_vzyUaU9SA_n6KSWxsPFoU7Q693iZf4QL5_uH-ezZaxYlnYxUxzTugZc8TSnHFeYSJwoVWdppUhS1jRRoZPnrKCsLhVRmcpxTkvKZDiFsAm6Hv4NW7334DvRaK_AGNmC7b2gjOGUFzjjAU0HVDnrvYNabJxupNsJgsXep1iLg0-x9ykGnyF3dRjRlw1Uf6lfgQG4HQAIh251iHuloVVQ6SCtE5XV_4z4AWhiikw</recordid><startdate>202003</startdate><enddate>202003</enddate><creator>Yun, Sang-Moon</creator><creator>Cho, Sun-Jung</creator><creator>Jo, Chulman</creator><creator>Park, Moon Ho</creator><creator>Han, Changsu</creator><creator>Koh, Young Ho</creator><general>Elsevier B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202003</creationdate><title>Elevation of plasma soluble amyloid precursor protein beta in Alzheimer’s disease</title><author>Yun, Sang-Moon ; Cho, Sun-Jung ; Jo, Chulman ; Park, Moon Ho ; Han, Changsu ; Koh, Young Ho</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-3c902ffe0d957290d01a04ccf65dc14bf24c1a0773823fbc1c6c7072b23a00013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Alzheimer’s disease (AD)</topic><topic>Cognitive impairment</topic><topic>Plasma biomarker</topic><topic>Soluble amyloid precursor proteins alpha (sAPPα)</topic><topic>Soluble amyloid precursor proteins beta (sAPPβ)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yun, Sang-Moon</creatorcontrib><creatorcontrib>Cho, Sun-Jung</creatorcontrib><creatorcontrib>Jo, Chulman</creatorcontrib><creatorcontrib>Park, Moon Ho</creatorcontrib><creatorcontrib>Han, Changsu</creatorcontrib><creatorcontrib>Koh, Young Ho</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Archives of gerontology and geriatrics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yun, Sang-Moon</au><au>Cho, Sun-Jung</au><au>Jo, Chulman</au><au>Park, Moon Ho</au><au>Han, Changsu</au><au>Koh, Young Ho</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Elevation of plasma soluble amyloid precursor protein beta in Alzheimer’s disease</atitle><jtitle>Archives of gerontology and geriatrics</jtitle><addtitle>Arch Gerontol Geriatr</addtitle><date>2020-03</date><risdate>2020</risdate><volume>87</volume><spage>103995</spage><epage>103995</epage><pages>103995-103995</pages><artnum>103995</artnum><issn>0167-4943</issn><eissn>1872-6976</eissn><abstract>•Plasma sAPPβ levels is higher in Alzheimer’s disease patients than in controls.•Plasma sAPPβ levels tends to increase with increasing cognitive impairment.•sAPPα and sAPPβ in plasma have a strong positive correlation, which is stronger in MCI and AD than in controls. Beta-amyloid is considered to be a pathophysiological marker in Alzheimer's disease (AD). Soluble amyloid precursor proteins (sAPPs) –α (sAPPα) and –β (sAPPβ), which are the byproducts of non-amyloidogenic and amyloidogenic process of APP, respectively, have been repeatedly observed in the cerebrospinal fluids (CSF) of AD patients. The present study focused on the determination of sAPP levels in peripheral blood. The plasma protein levels of sAPPα and sAPPβ were measured with ELISA. Plasma from 52 AD patients, 98 amnestic mild cognitive impairment (MCI) patients, and 114 cognitively normal controls were compared. The plasma level of sAPPβ was significantly increased in AD patients than in cognitively healthy controls. However, no significant change in plasma sAPPα was observed among the three groups. Furthermore, the plasma sAPPβ levels significantly correlated with cognitive assessment scales, such as clinical dementia rating (CDR), and mini-mental status examination (MMSE). 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subjects Alzheimer’s disease (AD)
Cognitive impairment
Plasma biomarker
Soluble amyloid precursor proteins alpha (sAPPα)
Soluble amyloid precursor proteins beta (sAPPβ)
title Elevation of plasma soluble amyloid precursor protein beta in Alzheimer’s disease
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