Network analysis of plasma proteomes in affective disorders.
Sang Jin RheeDongyoon ShinDaun ShinYoojin SongEun-Jeong JooHee Yeon JungSungwon RohSang-Hyuk LeeHyeyoung KimMinji BangKyu Young LeeJihyeon LeeJaenyeon KimYeongshin KimYoungsoo KimYong-Min AhnPublished in: Translational psychiatry (2023)
The conventional differentiation of affective disorders into major depressive disorder (MDD) and bipolar disorder (BD) has insufficient biological evidence. Utilizing multiple proteins quantified in plasma may provide critical insight into these limitations. In this study, the plasma proteomes of 299 patients with MDD or BD (aged 19-65 years old) were quantified using multiple reaction monitoring. Based on 420 protein expression levels, a weighted correlation network analysis was performed. Significant clinical traits with protein modules were determined using correlation analysis. Top hub proteins were determined using intermodular connectivity, and significant functional pathways were identified. Weighted correlation network analysis revealed six protein modules. The eigenprotein of a protein module with 68 proteins, including complement components as hub proteins, was associated with the total Childhood Trauma Questionnaire score (r = -0.15, p = 0.009). Another eigenprotein of a protein module of 100 proteins, including apolipoproteins as hub proteins, was associated with the overeating item of the Symptom Checklist-90-Revised (r = 0.16, p = 0.006). Functional analysis revealed immune responses and lipid metabolism as significant pathways for each module, respectively. No significant protein module was associated with the differentiation between MDD and BD. In conclusion, childhood trauma and overeating symptoms were significantly associated with plasma protein networks and should be considered important endophenotypes in affective disorders.
Keyphrases
- network analysis
- major depressive disorder
- bipolar disorder
- protein protein
- amino acid
- immune response
- binding protein
- gene expression
- magnetic resonance
- physical activity
- dna methylation
- toll like receptor
- cross sectional
- computed tomography
- bioinformatics analysis
- dendritic cells
- single cell
- psychometric properties
- functional connectivity