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Evaluation of a Nondepleted Plasma Multiprotein-Based Model for Discriminating Psychiatric Disorders Using Multiple Reaction Monitoring-Mass Spectrometry: Proof-of-Concept Study

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dc.contributor.authorShin, Dongyoon-
dc.contributor.authorLee, Jihyeon-
dc.contributor.authorKim, Yeongshin-
dc.contributor.authorPark, Junho-
dc.contributor.authorShin, Daun-
dc.contributor.authorSong, Yoojin-
dc.contributor.authorJoo, Eun-Jeong-
dc.contributor.authorRoh, Sungwon-
dc.contributor.authorLee, Kyu Young-
dc.contributor.authorOh, Sanghoon-
dc.contributor.authorAhn, Yong Min-
dc.contributor.authorRhee, Sang Jin-
dc.contributor.authorKim, Youngsoo-
dc.date.accessioned2024-11-28T15:01:44Z-
dc.date.available2024-11-28T15:01:44Z-
dc.date.issued2024-01-
dc.identifier.issn1535-3893-
dc.identifier.issn1535-3907-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/197119-
dc.description.abstractPsychiatric evaluation relies on subjective symptoms and behavioral observation, which sometimes leads to misdiagnosis. Despite previous efforts to utilize plasma proteins as objective markers, the depletion method is time-consuming. Therefore, this study aimed to enhance previous quantification methods and construct objective discriminative models for major psychiatric disorders using nondepleted plasma. Multiple reaction monitoring-mass spectrometry (MRM-MS) assays for quantifying 453 peptides in nondepleted plasma from 132 individuals [35 major depressive disorder (MDD), 47 bipolar disorder (BD), 23 schizophrenia (SCZ) patients, and 27 healthy controls (HC)] were developed. Pairwise discriminative models for MDD, BD, and SCZ, and a discriminative model between patients and HC were constructed by machine learning approaches. In addition, the proteins from nondepleted plasma-based discriminative models were compared with previously developed depleted plasma-based discriminative models. Discriminative models for MDD versus BD, BD versus SCZ, MDD versus SCZ, and patients versus HC were constructed with 11 to 13 proteins and showed reasonable performances (AUROC = 0.890-0.955). Most of the shared proteins between nondepleted and depleted plasma models had consistent directions of expression levels and were associated with neural signaling, inflammatory, and lipid metabolism pathways. These results suggest that multiprotein markers from nondepleted plasma have a potential role in psychiatric evaluation.-
dc.format.extent15-
dc.language영어-
dc.language.isoENG-
dc.publisherAmerican Chemical Society-
dc.titleEvaluation of a Nondepleted Plasma Multiprotein-Based Model for Discriminating Psychiatric Disorders Using Multiple Reaction Monitoring-Mass Spectrometry: Proof-of-Concept Study-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1021/acs.jproteome.3c00580-
dc.identifier.scopusid2-s2.0-85180091318-
dc.identifier.wosid001137566400001-
dc.identifier.bibliographicCitationJournal of Proteome Research, v.23, no.1, pp 329 - 343-
dc.citation.titleJournal of Proteome Research-
dc.citation.volume23-
dc.citation.number1-
dc.citation.startPage329-
dc.citation.endPage343-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiochemical Research Methods-
dc.subject.keywordPlusMAJOR DEPRESSIVE DISORDER-
dc.subject.keywordPlusPROTEOMIC ANALYSIS-
dc.subject.keywordPlusBIPOLAR DISORDER-
dc.subject.keywordPlusMENTAL-DISORDERS-
dc.subject.keywordPlusNETWORK ANALYSIS-
dc.subject.keywordPlusGLOBAL BURDEN-
dc.subject.keywordPlusPREVALENCE-
dc.subject.keywordPlusSCHIZOPHRENIA-
dc.subject.keywordPlusPROTEINS-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordAuthorbipolar disorder-
dc.subject.keywordAuthordiscriminative model-
dc.subject.keywordAuthormachine learning-
dc.subject.keywordAuthormajor depressive disorder-
dc.subject.keywordAuthorMRM-MS-
dc.subject.keywordAuthornondepleted plasma-
dc.subject.keywordAuthorschizophrenia-
dc.identifier.urlhttps://pubs.acs.org/doi/10.1021/acs.jproteome.3c00580-
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