Fernández-Pereira Carlos, Penedo Maria Aránzazu, Alonso-Núñez Adrián, Rivera-Baltanás Tania, Viéitez Irene, Prieto-González José María, Vilariño-Vilariño María Isabel, Olivares José Manuel, Ortolano Saida, Agís-Balboa Roberto Carlos
Translational Neuroscience Group, Galicia Sur Health Research Institute (IIS Galicia Sur), Área Sanitaria de Vigo-Hospital Álvaro Cunqueiro, SERGAS-UVIGO, CIBERSAM-ISCIII, Vigo, Spain.
Neuro Epigenetics Lab, Health Research Institute of Santiago de Compostela (IDIS), Santiago University Hospital Complex, Santiago de Compostela, Spain.
Front Pharmacol. 2024 Apr 24;15:1384198. doi: 10.3389/fphar.2024.1384198. eCollection 2024.
Bipolar disorder (BD) is a recurrent and disabling psychiatric disorder related to low-grade peripheral inflammation and altered levels of the members of the insulin-like growth factor (IGF) family. The aim of this study was to evaluate the plasma levels of IGF-2, insulin-like growth factor-binding protein 1 (IGFBP-1), IGFBP-3, IGFBP-5, IGFBP-7, and inflammatory markers such as tumor necrosis factor α (TNF-α), monocyte chemoattractant protein 1 (MCP-1), and macrophage inflammatory protein 1β (MIP-1β). We used the Young Mania Rating Scale (YMRS) to determine the severity of the symptomatology, while proteins were measured by enzyme-linked immunosorbent assay (ELISA). We included 20 patients with BD who suffered a manic episode and 20 controls. Some BD patients ( = 10) were evaluated after a period (17 ± 8 days) of pharmacological treatment. No statistical difference was found in IGF-2, IGFBP-1, IGFBP-7, TNF-α, and MIP-1β levels. However, IGFBP-3 and IGFBP-5 levels were found to be statistically decreased in BD patients. Conversely, the MCP-1 level was significantly increased in BD patients, but their levels were normalized after treatment. Intriguingly, only IGFBP-1 levels were significantly decreased after treatment. No significant correlation was found between the YMRS and any of the proteins studied either before or after treatment or between IGF proteins and inflammatory markers. To some extent, IGFBP-3 and IGFBP-5 might be further explored as potential indicators of treatment responsiveness or diagnosis biomarkers in BD.
双相情感障碍(BD)是一种复发性且致残的精神疾病,与低度外周炎症以及胰岛素样生长因子(IGF)家族成员水平的改变有关。本研究的目的是评估血浆中IGF-2、胰岛素样生长因子结合蛋白1(IGFBP-1)、IGFBP-3、IGFBP-5、IGFBP-7的水平,以及肿瘤坏死因子α(TNF-α)、单核细胞趋化蛋白1(MCP-1)和巨噬细胞炎性蛋白1β(MIP-1β)等炎症标志物的水平。我们使用青年躁狂评定量表(YMRS)来确定症状的严重程度,同时通过酶联免疫吸附测定(ELISA)来检测蛋白质。我们纳入了20例经历过躁狂发作的双相情感障碍患者和20名对照者。部分双相情感障碍患者(n = 10)在经过一段时间(17±8天)的药物治疗后接受了评估。在IGF-2、IGFBP-1、IGFBP-7、TNF-α和MIP-1β水平方面未发现统计学差异。然而,发现双相情感障碍患者的IGFBP-3和IGFBP-5水平在统计学上有所降低。相反,双相情感障碍患者的MCP-1水平显著升高,但治疗后其水平恢复正常。有趣的是,仅治疗后IGFBP-1水平显著降低。在治疗前或治疗后,YMRS与所研究的任何蛋白质之间,以及IGF蛋白与炎症标志物之间均未发现显著相关性。在某种程度上,IGFBP-3和IGFBP-5可能作为双相情感障碍治疗反应性的潜在指标或诊断生物标志物有待进一步探索。