Metabolomic profiling of serum in the progression of Alzheimer's disease by capillary electrophoresis-mass spectrometry
There is high interest in the discovery of early diagnostic biomarkers of Alzheimer's disease, for which metabolomics exhibits a great potential. In this work, a metabolomic approach based on ultrafiltration and analysis by CE‐MS has been used to obtain representative fingerprints of polar meta...
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Veröffentlicht in: | Electrophoresis 2014-12, Vol.35 (23), p.3321-3330 |
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description | There is high interest in the discovery of early diagnostic biomarkers of Alzheimer's disease, for which metabolomics exhibits a great potential. In this work, a metabolomic approach based on ultrafiltration and analysis by CE‐MS has been used to obtain representative fingerprints of polar metabolites from serum samples in order to distinguish between patients with Alzheimer's disease, mild cognitive impairment, and healthy controls. By the use of partial least squares discriminant analysis it was possible to classify patients according to the disease stage and then identify potential markers. Significant increase was observed with progression of disease in levels of choline, creatinine, asymmetric dimethyl‐arginine, homocysteine‐cysteine disulfide, phenylalanyl‐phenylalanine, and different medium chain acylcarnitines. On the other hand, asparagine, methionine, histidine, carnitine, acetyl‐spermidine, and C5‐carnitine were reduced in these serum samples. In this way, multiple essential pathways were found implicated in the underlying pathology, such as oxidative stress or defects in energy metabolism. However, the most interesting results are related to the association of several vascular risk factors with Alzheimer's disease. |
doi_str_mv | 10.1002/elps.201400196 |
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In this work, a metabolomic approach based on ultrafiltration and analysis by CE‐MS has been used to obtain representative fingerprints of polar metabolites from serum samples in order to distinguish between patients with Alzheimer's disease, mild cognitive impairment, and healthy controls. By the use of partial least squares discriminant analysis it was possible to classify patients according to the disease stage and then identify potential markers. Significant increase was observed with progression of disease in levels of choline, creatinine, asymmetric dimethyl‐arginine, homocysteine‐cysteine disulfide, phenylalanyl‐phenylalanine, and different medium chain acylcarnitines. On the other hand, asparagine, methionine, histidine, carnitine, acetyl‐spermidine, and C5‐carnitine were reduced in these serum samples. In this way, multiple essential pathways were found implicated in the underlying pathology, such as oxidative stress or defects in energy metabolism. However, the most interesting results are related to the association of several vascular risk factors with Alzheimer's disease.</description><identifier>ISSN: 0173-0835</identifier><identifier>EISSN: 1522-2683</identifier><identifier>DOI: 10.1002/elps.201400196</identifier><identifier>PMID: 25136972</identifier><language>eng</language><publisher>Germany: Blackwell Publishing Ltd</publisher><subject>Aged ; Aged, 80 and over ; Alzheimer Disease - blood ; Alzheimer Disease - metabolism ; Alzheimer's disease ; Biomarkers - blood ; CE-MS ; Cognitive Dysfunction ; Discriminant analysis ; Electrophoresis ; Electrophoresis, Capillary - methods ; Female ; Fingerprints ; Humans ; Male ; Mass Spectrometry - methods ; Metabolome ; Metabolomics ; Metabolomics - methods ; Mild cognitive impairment ; Patients ; Progressions ; Risk ; Serums</subject><ispartof>Electrophoresis, 2014-12, Vol.35 (23), p.3321-3330</ispartof><rights>2014 WILEY‐VCH Verlag GmbH & Co. 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KGaA, Weinheim.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4775-4ca0c5e479634b799bb8006e4071fee4d7638089032d0f13a4a9e369bff8bf793</citedby><cites>FETCH-LOGICAL-c4775-4ca0c5e479634b799bb8006e4071fee4d7638089032d0f13a4a9e369bff8bf793</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Felps.201400196$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Felps.201400196$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25136972$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>González-Domínguez, Raúl</creatorcontrib><creatorcontrib>García, Antonia</creatorcontrib><creatorcontrib>García-Barrera, Tamara</creatorcontrib><creatorcontrib>Barbas, Coral</creatorcontrib><creatorcontrib>Gómez-Ariza, José Luis</creatorcontrib><title>Metabolomic profiling of serum in the progression of Alzheimer's disease by capillary electrophoresis-mass spectrometry</title><title>Electrophoresis</title><addtitle>ELECTROPHORESIS</addtitle><description>There is high interest in the discovery of early diagnostic biomarkers of Alzheimer's disease, for which metabolomics exhibits a great potential. In this work, a metabolomic approach based on ultrafiltration and analysis by CE‐MS has been used to obtain representative fingerprints of polar metabolites from serum samples in order to distinguish between patients with Alzheimer's disease, mild cognitive impairment, and healthy controls. By the use of partial least squares discriminant analysis it was possible to classify patients according to the disease stage and then identify potential markers. Significant increase was observed with progression of disease in levels of choline, creatinine, asymmetric dimethyl‐arginine, homocysteine‐cysteine disulfide, phenylalanyl‐phenylalanine, and different medium chain acylcarnitines. On the other hand, asparagine, methionine, histidine, carnitine, acetyl‐spermidine, and C5‐carnitine were reduced in these serum samples. In this way, multiple essential pathways were found implicated in the underlying pathology, such as oxidative stress or defects in energy metabolism. However, the most interesting results are related to the association of several vascular risk factors with Alzheimer's disease.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Alzheimer Disease - blood</subject><subject>Alzheimer Disease - metabolism</subject><subject>Alzheimer's disease</subject><subject>Biomarkers - blood</subject><subject>CE-MS</subject><subject>Cognitive Dysfunction</subject><subject>Discriminant analysis</subject><subject>Electrophoresis</subject><subject>Electrophoresis, Capillary - methods</subject><subject>Female</subject><subject>Fingerprints</subject><subject>Humans</subject><subject>Male</subject><subject>Mass Spectrometry - methods</subject><subject>Metabolome</subject><subject>Metabolomics</subject><subject>Metabolomics - methods</subject><subject>Mild cognitive impairment</subject><subject>Patients</subject><subject>Progressions</subject><subject>Risk</subject><subject>Serums</subject><issn>0173-0835</issn><issn>1522-2683</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc1v00AQxVcIRNPClSPaG1wcZr-83mMVSosUoBKgclutnXGzYMfujqMS_no2pOQKp5Fmfu9pnh5jLwTMBYB8g91IcwlCAwhXPmIzYaQsZFmpx2wGwqoCKmVO2CnRdwDQTuun7EQaoUpn5Yzdf8Ap1EM39LHhYxra2MXNLR9aTpi2PY8bPq1xf7lNSBSHzf523v1aY-wxvSK-ioSBkNc73oQxdl1IO44dNlMaxvWQVZGKPhBxGv8se5zS7hl70oaO8PnDPGNf3118WVwVy0-X7xfny6LR1ppCNwEag9q6UunaOlfXFUCJGqxoEfXKlqqCyoGSK2iFCjo4zNHqtq3q1jp1xl4ffHOCuy3S5PtIDeYvNzhsyYvSCC1MqeE_UOnyG7KyGZ0f0CYNRAlbP6bY5-BegN_34ve9-GMvWfDywXtb97g64n-LyIA-APexw90_7PzF8vqzkcZkWXGQRZrw51EW0g9fWmWNv_l46d8u7PU3BcrfqN9lMKn1</recordid><startdate>201412</startdate><enddate>201412</enddate><creator>González-Domínguez, Raúl</creator><creator>García, Antonia</creator><creator>García-Barrera, Tamara</creator><creator>Barbas, Coral</creator><creator>Gómez-Ariza, José Luis</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</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>7U5</scope><scope>8FD</scope><scope>L7M</scope></search><sort><creationdate>201412</creationdate><title>Metabolomic profiling of serum in the progression of Alzheimer's disease by capillary electrophoresis-mass spectrometry</title><author>González-Domínguez, Raúl ; 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In this work, a metabolomic approach based on ultrafiltration and analysis by CE‐MS has been used to obtain representative fingerprints of polar metabolites from serum samples in order to distinguish between patients with Alzheimer's disease, mild cognitive impairment, and healthy controls. By the use of partial least squares discriminant analysis it was possible to classify patients according to the disease stage and then identify potential markers. Significant increase was observed with progression of disease in levels of choline, creatinine, asymmetric dimethyl‐arginine, homocysteine‐cysteine disulfide, phenylalanyl‐phenylalanine, and different medium chain acylcarnitines. On the other hand, asparagine, methionine, histidine, carnitine, acetyl‐spermidine, and C5‐carnitine were reduced in these serum samples. In this way, multiple essential pathways were found implicated in the underlying pathology, such as oxidative stress or defects in energy metabolism. 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subjects | Aged Aged, 80 and over Alzheimer Disease - blood Alzheimer Disease - metabolism Alzheimer's disease Biomarkers - blood CE-MS Cognitive Dysfunction Discriminant analysis Electrophoresis Electrophoresis, Capillary - methods Female Fingerprints Humans Male Mass Spectrometry - methods Metabolome Metabolomics Metabolomics - methods Mild cognitive impairment Patients Progressions Risk Serums |
title | Metabolomic profiling of serum in the progression of Alzheimer's disease by capillary electrophoresis-mass spectrometry |
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