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Plasma soluble neuregulin-1 as a diagnostic biomarker for Alzheimer's disease
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dc.contributor.author Chang, Keun-A -
dc.contributor.author Shin, Ki Young -
dc.contributor.author Nam, Eunjoo -
dc.contributor.author Lee, Yeong-Bae -
dc.contributor.author Moon, Cheil -
dc.contributor.author Suh, Yoo-Hun -
dc.contributor.author Lee, Sang Hyung -
dc.date.accessioned 2021-04-23T06:31:43Z -
dc.date.available 2021-04-23T06:31:43Z -
dc.date.created 2018-03-29 -
dc.date.issued 2016-07 -
dc.identifier.issn 0197-0186 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/13325 -
dc.description.abstract To identify some apparent biomarker candidates for the diagnosis of Alzheimer's disease (AD) pathology, we investigated whether there would be a significant difference between the levels of the plasma proteins of AD patients and healthy people. A total of 115 subjects were enrolled, 60 individuals with AD and 55 healthy controls. There was a statistical difference in the mini-mental status exam (MMSE) scores and the clinical dementia rating (CDR) scores between the two groups. We used the immunoblotting assay to analyze several plasma proteins in the subjects. Amyloid-β (Aβ), S100a9, and soluble neuregulin-1 (sNRG-1), including α-synuclein (α-Syn) as a detection control were detected in the plasma samples. Unlike Aβ, S100a9 and α-Syn, the level of sNRG-1 of the AD patients was significantly higher than that of the healthy control subjects. The AD patients were divided into mild and moderate groups according to their MMSE and CDR scores. We found a significant correlation between the level of sNRG-1 and MMSE scores. The sNRG-1 level was significantly higher in mild AD patients as well as in moderate AD patients compared with that of the control subjects. These new findings indicate that increased plasma sNRG-1 levels might be a novel and reliable biological marker for the early diagnosis of AD. © 2016 Elsevier Ltd. All rights reserved. -
dc.language English -
dc.publisher Oxford University Press -
dc.title Plasma soluble neuregulin-1 as a diagnostic biomarker for Alzheimer's disease -
dc.type Article -
dc.identifier.doi 10.1016/j.neuint.2016.04.012 -
dc.identifier.wosid 000379559000001 -
dc.identifier.scopusid 2-s2.0-84965105405 -
dc.identifier.bibliographicCitation Neurochemistry International, v.97, pp.1 - 7 -
dc.description.isOpenAccess FALSE -
dc.subject.keywordAuthor Alzheimer&apos -
dc.subject.keywordAuthor s disease -
dc.subject.keywordAuthor Beta amyloid -
dc.subject.keywordAuthor Soluble NRG-1 -
dc.subject.keywordAuthor Blood plasma -
dc.subject.keywordAuthor Biomarker -
dc.subject.keywordPlus MILD COGNITIVE IMPAIRMENT -
dc.subject.keywordPlus AMYLOID-BETA -
dc.subject.keywordPlus INFLAMMATORY S100A9 -
dc.subject.keywordPlus PERIPHERAL MARKER -
dc.subject.keywordPlus HEPARAN-SULFATE -
dc.subject.keywordPlus SPINAL-CORD -
dc.subject.keywordPlus HUMAN BRAIN -
dc.subject.keywordPlus IN-VITRO -
dc.subject.keywordPlus EXPRESSION -
dc.subject.keywordPlus PROTEINS -
dc.citation.endPage 7 -
dc.citation.startPage 1 -
dc.citation.title Neurochemistry International -
dc.citation.volume 97 -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.relation.journalResearchArea Biochemistry & Molecular Biology; Neurosciences & Neurology -
dc.relation.journalWebOfScienceCategory Biochemistry & Molecular Biology; Neurosciences -
dc.type.docType Article -
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