Department of Bipolar Disorders, Clinic for Psychiatry, University Clinical Centre of Serbia, Pasterova 2, 11000 Belgrade, Serbia.
School of Medicine, University of Belgrade, Dr Subotica 8 st., 11000 Belgrade, Serbia.
Cells. 2024 Jul 18;13(14):1213. doi: 10.3390/cells13141213.
Increased immune-inflammatory activation has been repeatedly linked to etiopathogenesis and the progression of both major depressive disorder (MDD) and bipolar depression (BD). We explore the role of soluble intercellular cell adhesion molecule-1 (sICAM-1) and soluble vascular cell adhesion molecule-1 (sVCAM-1) in diagnostic differentiation and disorder progression in patients with MDD and BD. Serum levels of sICAM-1 and sVCAM-1 were measured in 137 patients (MDD = 93 and BD = 44) and compared with 73 healthy controls. The severity of psychopathology was assessed using the Hamilton Depression Rating Scale and Clinical Global Impression Scale. After adjustment for multiple confounders, we noticed significant downregulation of sVCAM-1 and upregulation of sICAM-1 levels in both patient groups. Decreased sVCAM-1 levels were detected in patients with acute episodes of BD when compared to MDD. Immune mediators were related to indicators of progression in both mood disorders. They also followed different post-treatment normalization patterns in MDD and BD and in relation to the stage of each disorder. Adhesion molecules could potentially be useful in discriminating between patients with MDD and BD and determining the possible progression of the disorders. Future nosological methods should include time-dependent pathoplasticity and biological correlates, at least for affective disorders.
免疫炎症激活与重性抑郁障碍(MDD)和双相抑郁障碍(BD)的发病机制和进展均密切相关。本研究旨在探讨可溶性细胞间黏附分子-1(sICAM-1)和可溶性血管细胞黏附分子-1(sVCAM-1)在 MDD 和 BD 患者的诊断区分和疾病进展中的作用。检测了 137 例患者(MDD=93 例,BD=44 例)和 73 例健康对照者的血清 sICAM-1 和 sVCAM-1 水平。采用汉密尔顿抑郁量表和临床总体印象量表评估精神病理学严重程度。校正多种混杂因素后,我们发现两组患者的 sVCAM-1 水平显著下调,sICAM-1 水平显著上调。与 MDD 相比,BD 急性发作患者的 sVCAM-1 水平降低。免疫介质与两种心境障碍的进展指标相关。它们还与每种疾病的阶段有关,在 MDD 和 BD 以及与治疗后正常化模式不同。黏附分子可能有助于区分 MDD 和 BD 患者,并确定疾病的可能进展。未来的分类方法应至少包括与情感障碍相关的时间依赖性病理可塑性和生物学相关性。