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Quantitative Proteomic Approach for Discriminating Major Depressive Disorder and Bipolar Disorder by Multiple Reaction Monitoring-Mass Spectrometry

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dc.contributor.authorShin, Dongyoon-
dc.contributor.authorRhee, Sang Jin-
dc.contributor.authorLee, Jihyeon-
dc.contributor.authorYeo, Injoon-
dc.contributor.authorDo, Misol-
dc.contributor.authorJoo, Eun-Jeong-
dc.contributor.authorJung, Hee Yeo-
dc.contributor.authorRoh, Sung won-
dc.contributor.authorLee, Sang-Hyuk-
dc.contributor.authorKim, Hyeyoung-
dc.contributor.authorBang, Minji-
dc.contributor.authorLee, Kyu Young-
dc.contributor.authorKwon, Jun Soo-
dc.contributor.authorHa, Kyooseob-
dc.contributor.authorAhn, Yong Min-
dc.contributor.authorKim, Youngsoo-
dc.date.accessioned2022-07-06T17:19:49Z-
dc.date.available2022-07-06T17:19:49Z-
dc.date.created2021-07-14-
dc.date.issued2021-06-
dc.identifier.issn1535-3893-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/141779-
dc.description.abstractBecause major depressive disorder (MDD) and bipolar disorder (BD) manifest with similar symptoms, misdiagnosis is a persistent issue, necessitating their differentiation through objective methods. This study was aimed to differentiate between these disorders using a targeted proteomic approach. Multiple reaction monitoring-mass spectrometry (MRM-MS) analysis was performed to quantify protein targets regarding the two disorders in plasma samples of 270 individuals (90 MDD, 90 BD, and 90 healthy controls (HCs)). In the training set (72 MDD and 72 BD), a generalizable model comprising nine proteins was developed. The model was evaluated in the test set (18 MDD and 18 BD). The model demonstrated a good performance (area under the curve (AUC) >0.8) in discriminating MDD from BD in the training (AUC = 0.84) and test sets (AUC = 0.81) and in distinguishing MDD from BD without current hypomanic/manic/mixed symptoms (90 MDD and 75 BD) (AUC = 0.83). Subsequently, the model demonstrated excellent performance for drug-free MDD versus BD (11 MDD and 10 BD) (AUC = 0.96) and good performance for MDD versus HC (AUC = 0.87) and BD versus HC (AUC = 0.86). Furthermore, the nine proteins were associated with neuro, oxidative/nitrosative stress, and immunity/inflammation-related biological functions. This proof-of-concept study introduces a potential model for distinguishing between the two disorders.-
dc.language영어-
dc.language.isoen-
dc.publisherAmerican Chemical Society-
dc.titleQuantitative Proteomic Approach for Discriminating Major Depressive Disorder and Bipolar Disorder by Multiple Reaction Monitoring-Mass Spectrometry-
dc.typeArticle-
dc.contributor.affiliatedAuthorRoh, Sung won-
dc.identifier.doi10.1021/acs.jproteome.1c00058-
dc.identifier.scopusid2-s2.0-85106463122-
dc.identifier.wosid000661127000016-
dc.identifier.bibliographicCitationJournal of Proteome Research, v.20, no.6, pp.3188 - 3203-
dc.relation.isPartOfJournal of Proteome Research-
dc.citation.titleJournal of Proteome Research-
dc.citation.volume20-
dc.citation.number6-
dc.citation.startPage3188-
dc.citation.endPage3203-
dc.type.rimsART-
dc.type.docTypeArticle in Press-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiochemical Research Methods-
dc.subject.keywordPlusGENOME-WIDE ASSOCIATION-
dc.subject.keywordPlusHEPATOCELLULAR-CARCINOMA-
dc.subject.keywordPlusBETA-THROMBOGLOBULIN-
dc.subject.keywordPlusSERUM-
dc.subject.keywordPlusPLASMA-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordPlusPROTEINS-
dc.subject.keywordPlusBIOMARKERS-
dc.subject.keywordPlusPATHWAYS-
dc.subject.keywordPlusC1Q-
dc.subject.keywordAuthorbipolar disorder (BD)-
dc.subject.keywordAuthorgeneralizable model-
dc.subject.keywordAuthormajor depressive disorder (MDD)-
dc.subject.keywordAuthormultiple reaction monitoring-mass spectrometry (MRM-MS)-
dc.subject.keywordAuthorquantitative targeted proteomics-
dc.identifier.urlhttps://pubs.acs.org/doi/10.1021/acs.jproteome.1c00058-
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