Fleury Samuel, Schnitzer Mireille E, Ledoux-Hutchinson Lawrence, Boukhatem Imane, Bélanger Jean-Christophe, Welman Mélanie, Busseuil David, Tardif Jean-Claude, D'Antono Bianca, Lordkipanidzé Marie
Research Centre, Montreal Heart Institute, Montreal, QC, Canada.
Faculty of Pharmacy, Université de Montréal, Montreal, QC, Canada.
Front Aging Neurosci. 2022 Feb 21;14:821865. doi: 10.3389/fnagi.2022.821865. eCollection 2022.
The p75 receptor binds all neurotrophins and is mostly known for its role in neuronal survival and apoptosis. Recently, the extracellular domain (ECD) of p75 has been reported in plasma, its levels being dysregulated in numerous neurological diseases. However, the factors associated with p75 ECD levels remain unknown. We investigated clinical correlates of plasma p75 ECD levels in older adults without clinically manifested neurological disorders. Circulating p75 levels were measured by enzyme-linked immunosorbent assay in plasma obtained from participants in the BEL-AGE cohort ( = 1,280). Determinants of plasma p75 ECD levels were explored using linear and non-linear statistical models. Plasma p75 ECD levels were higher in male participants; were positively correlated with circulating concentrations of pro-brain-derived neurotrophic factor, and inflammatory markers interleukin-6 and CD40 Ligand; and were negatively correlated with the platelet activation marker P-selectin. While most individuals had p75 levels ranging from 43 to 358 pg/ml, high p75 levels reaching up to 9,000 pg/ml were detectable in a subgroup representing 15% of the individuals studied. In this cohort of older adults without clinically manifested neurological disorders, there was no association between plasma p75 ECD levels and cognitive performance, as assessed by the Montreal Cognitive Assessment score. The physiological relevance of high p75 ECD levels in plasma warrants further investigation. Further research assessing the source of circulating p75 is needed for a deeper understanding of the direction of effect, and to investigate whether high p75 ECD levels are predictive biomarkers or consequences of neuropathology.
p75受体可结合所有神经营养因子,其在神经元存活和凋亡中的作用最为人所知。最近,有报道称p75的细胞外结构域(ECD)存在于血浆中,其水平在多种神经系统疾病中失调。然而,与p75 ECD水平相关的因素仍然未知。我们调查了无临床表现的神经系统疾病的老年人血浆p75 ECD水平的临床相关性。通过酶联免疫吸附测定法测量了从BEL-AGE队列(n = 1280)参与者获得的血浆中循环p75水平。使用线性和非线性统计模型探索血浆p75 ECD水平的决定因素。男性参与者的血浆p75 ECD水平较高;与脑源性神经营养因子前体、炎症标志物白细胞介素-6和CD40配体的循环浓度呈正相关;与血小板活化标志物P-选择素呈负相关。虽然大多数个体的p75水平在43至358 pg/ml之间,但在占研究个体15%的一个亚组中可检测到高达9000 pg/ml的高p75水平。在这个无临床表现的神经系统疾病的老年人群体中,根据蒙特利尔认知评估得分评估,血浆p75 ECD水平与认知表现之间没有关联。血浆中高p75 ECD水平的生理相关性值得进一步研究。需要进一步研究评估循环p75的来源,以更深入地了解其作用方向,并调查高p75 ECD水平是否为预测性生物标志物或神经病理学的后果。