Fernández-Pereira Carlos, Agís-Balboa Roberto Carlos
Neuro Epigenetics Lab, Health Research Institute of Santiago de Compostela (IDIS), Santiago University Hospital Complex, 15706 Santiago de Compostela, Spain.
Translational Research in Neurological Diseases (ITEN) Group, Health Research Institute of Santiago de Compostela (IDIS), Santiago University Hospital Complex, SERGAS-USC, 15706 Santiago de Compostela, Spain.
Int J Mol Sci. 2025 Mar 12;26(6):2561. doi: 10.3390/ijms26062561.
Psychiatric disorders (PDs), including schizophrenia (SZ), major depressive disorder (MDD), bipolar disorder (BD), autism spectrum disorder (ASD), among other disorders, represent a significant global health burden. Despite advancements in understanding their biological mechanisms, there is still no reliable objective and reliable biomarker; therefore, diagnosis remains largely reliant on subjective clinical assessments. Peripheral biomarkers in plasma or serum are interesting due to their accessibility, low cost, and potential to reflect central nervous system processes. Among these, the insulin-like growth factor (IGF) family, IGF-1, IGF-2, and IGF-binding proteins (IGFBPs), has gained attention for its roles in neuroplasticity, cognition, and neuroprotection, as well as for their capability to cross the blood-brain barrier. This review evaluates the evidence for IGF family alterations in PDs, with special focus on SZ, MDD, and BD, while also addressing other PDs covering almost 40 years of history. In SZ patients, IGF-1 alterations have been linked to metabolic dysregulation, treatment response, and hypothalamic-pituitary-adrenal axis dysfunction. In MDD patients, IGF-1 appears to compensate for impaired neurogenesis, although findings are inconsistent. Emerging studies on IGF-2 and IGFBPs suggest potential roles across PDs. While promising, heterogeneity among studies and methodological limitations highlights the need for further research to validate IGFs as reliable psychiatric biomarkers.
精神疾病(PDs),包括精神分裂症(SZ)、重度抑郁症(MDD)、双相情感障碍(BD)、自闭症谱系障碍(ASD)以及其他疾病,是全球重大的健康负担。尽管在了解其生物学机制方面取得了进展,但仍没有可靠的客观生物标志物;因此,诊断在很大程度上仍依赖于主观临床评估。血浆或血清中的外周生物标志物因其易获取、成本低以及反映中枢神经系统过程的潜力而备受关注。其中,胰岛素样生长因子(IGF)家族,即IGF-1、IGF-2和IGF结合蛋白(IGFBPs),因其在神经可塑性、认知和神经保护中的作用以及穿过血脑屏障的能力而受到关注。本综述评估了PDs中IGF家族改变的证据,特别关注SZ、MDD和BD,同时也涉及其他PDs,涵盖了近40年的历史。在SZ患者中,IGF-1的改变与代谢失调、治疗反应和下丘脑-垂体-肾上腺轴功能障碍有关。在MDD患者中,尽管研究结果不一致,但IGF-1似乎可以补偿受损的神经发生。关于IGF-2和IGFBPs的新兴研究表明它们在各种PDs中可能发挥作用。虽然前景广阔,但研究之间的异质性和方法学局限性凸显了进一步研究以验证IGFs作为可靠精神生物标志物的必要性。