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

Cited 8 time in Web of Science Cited 8 time in Scopus
Authors

Shin, Dongyoon; Rhee, Sang Jin; Lee, Jihyeon; Yeo, Injoon; Do, Misol; Joo, Eun-Jeong; Jung, Hee Yeon; Roh, Sungwon; Lee, Sang-Hyuk; Kim, Hyeyoung; Bang, Minji; Lee, Kyu Young; Kwon, Jun Soo; Ha, Kyooseob; Ahn, Yong Min; Kim, Youngsoo

Issue Date
2021-06
Publisher
American Chemical Society
Citation
Journal of Proteome Research, Vol.20 No.6, pp.3188-3203
Abstract
Because 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.
ISSN
1535-3893
URI
https://hdl.handle.net/10371/180114
DOI
https://doi.org/10.1021/acs.jproteome.1c00058
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