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Decreased plasma α-synuclein in idiopathic Parkinson’s disease patients after adjusting hemolysis factor

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dc.contributor.authorShim, K.H.-
dc.contributor.authorKim, S.C.-
dc.contributor.authorYoun, Y.C.-
dc.contributor.authorSung, Y.-H.-
dc.contributor.authorAn, S.S.A.-
dc.date.available2020-10-20T00:58:20Z-
dc.date.created2020-09-24-
dc.date.issued2020-11-
dc.identifier.issn1738-642X-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/78298-
dc.description.abstractBackground: Lewy bodies are pathological hallmarks for the diagnosis of Parkinson’s disease, where the core components are composed of aggregated forms of α-synuclein (α-syn). Although α-syn has been investigated as a potential biomarker for PD, its usage has been limited and still remains controversial. Objective: An accurate enzyme-linked immunosorbent assay (ELISA) was developed for the detection of α-syn in plasma. The hemolysis score was calculated to eliminate the additive α-syn levels from RBCs. Human plasma samples were collected in heparinized blood tubes from idiopathic Parkinson disease (IPD) and healthy control (HC). Result: Hemolysis score had a strong correlation with the level of plasma α-syn. From the limited set of samples in this preliminary study, decreased α-syn concentrations were observed in patients with IPD in comparison to HC after adjusting for hemolysis factor. Similar results with a commercial ELISA kit were found for measuring α-syn from the same set of samples with lower correlation and the reduced accuracy of diagnosis than the current study. Conclusion: The adjustments for the hemolysis factor would be indispensable, supporting plasma α-syn as a potential surrogate biomarker for distinguishing IPD from HC. © 2020, The Korean Society of Toxicogenomics and Toxicoproteomics 2020.-
dc.language영어-
dc.language.isoen-
dc.publisherSpringer Verlag-
dc.relation.isPartOfMolecular and Cellular Toxicology-
dc.titleDecreased plasma α-synuclein in idiopathic Parkinson’s disease patients after adjusting hemolysis factor-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000569534700001-
dc.identifier.doi10.1007/s13273-020-00104-7-
dc.identifier.bibliographicCitationMolecular and Cellular Toxicology, v.16, no.4, pp.477 - 484-
dc.identifier.kciidART002631296-
dc.description.isOpenAccessN-
dc.identifier.scopusid2-s2.0-85090929477-
dc.citation.endPage484-
dc.citation.startPage477-
dc.citation.titleMolecular and Cellular Toxicology-
dc.citation.volume16-
dc.citation.number4-
dc.contributor.affiliatedAuthorKim, S.C.-
dc.contributor.affiliatedAuthorSung, Y.-H.-
dc.contributor.affiliatedAuthorAn, S.S.A.-
dc.type.docTypeArticle-
dc.subject.keywordAuthorHemolysis-
dc.subject.keywordAuthorParkinson’s disease-
dc.subject.keywordAuthorα-Synuclein-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
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