Ioannou Magdalini, Borkent Jenny, Severance Emily G, Yolken Robert H, Fasano Alessio, Sommer Iris E C, Haarman Bartholomeus C M
Department of Psychiatry, University of Groningen and University Medical Centre Groningen, Groningen, the Netherlands; Department of Biomedical Sciences, University of Groningen and University Medical Centre Groningen, Groningen, the Netherlands.
Department of Biomedical Sciences, University of Groningen and University Medical Centre Groningen, Groningen, the Netherlands.
Prog Neuropsychopharmacol Biol Psychiatry. 2025 Jun 20;139:111405. doi: 10.1016/j.pnpbp.2025.111405. Epub 2025 May 26.
Zonulin, lipopolysaccharide-binding protein (LBP), and soluble CD14 (sCD14) are frequently used as proxy biomarkers of intestinal permeability in studies involving patients with psychiatric disorders. Although often used interchangeably, these biomarkers reflect distinct biological processes.
This review integrates evidence from basic research on the mechanisms of action of zonulin, LBP, and sCD14 with findings from studies on major depressive disorder, bipolar disorder, and schizophrenia spectrum disorders, aiming to refine their application in gut-brain axis research.
Zonulin is consistently elevated in schizophrenia spectrum disorders and appears most closely linked to gut barrier integrity and systemic immune activation. LBP is consistently elevated in major depressive disorder and may reflect underlying alterations in gut permeability, metabolic status, and psychological stress. sCD14 has been primarily studied in schizophrenia spectrum disorders, where findings are more heterogeneous, and is thought to reflect generalized monocyte activation. These biomarkers were largely unrelated to clinical symptom severity, with the exception of sCD14, which showed associations with positive symptoms, aggression, and the number of manic episodes.
Zonulin, LBP, and sCD14 each capture unique aspects of gut and immune system function. Their interchangeable use risks misinterpretation. A more nuanced, context-dependent application-tailored to specific research questions or intervention targets-is essential for advancing gut-brain axis research in psychiatry.
在涉及精神疾病患者的研究中,闭合蛋白、脂多糖结合蛋白(LBP)和可溶性CD14(sCD14)常被用作肠道通透性的替代生物标志物。尽管这些生物标志物经常互换使用,但它们反映的是不同的生物学过程。
本综述整合了关于闭合蛋白、LBP和sCD14作用机制的基础研究证据以及关于重度抑郁症、双相情感障碍和精神分裂症谱系障碍的研究结果,旨在优化它们在肠-脑轴研究中的应用。
闭合蛋白在精神分裂症谱系障碍中持续升高,似乎与肠道屏障完整性和全身免疫激活关系最为密切。LBP在重度抑郁症中持续升高,可能反映了肠道通透性、代谢状态和心理压力的潜在改变。sCD14主要在精神分裂症谱系障碍中进行了研究,研究结果更为多样,被认为反映了全身性单核细胞激活。除了sCD14与阳性症状、攻击性和躁狂发作次数有关外,这些生物标志物在很大程度上与临床症状严重程度无关。
闭合蛋白、LBP和sCD14各自反映了肠道和免疫系统功能的独特方面。互换使用它们可能会导致误解。为推进精神病学中的肠-脑轴研究,根据具体研究问题或干预目标进行更细致入微、因地制宜的应用至关重要。