Life and Health Sciences Research Institute, School of Medicine, University of Minho, Braga, Portugal.
ICVS/3B's - PT Government Associate Laboratory, Braga/Guimarães, Portugal.
Front Immunol. 2020 Sep 2;11:2045. doi: 10.3389/fimmu.2020.02045. eCollection 2020.
Cognition in the elderly is heterogeneous. Senescence of the immune system is increasingly considered as a potential player in cognitive performance. We explored here the interplay between cognitive performance and peripheral immune molecules in healthy older individuals.
A cross-sectional study of clinically well characterized senior healthy individuals (120; 51-87 years old) previously clustered as "Good" and "Poor" performers based on established tests that evaluate memory and executive function. A plasma concentration of 30 immune molecules was assessed by multiplex analysis and correlated with parameters of cognitive performance.
Participants with worse cognitive performance ("Poor") exhibited increased concentrations of IL-1β, IL-8, IL-13, and tumor necrosis factor (TNF) when compared to individuals with a better cognitive performance ("Good"). The cognitive dimensions memory and executive function, when considered separately, displayed a negative association with several immune molecules (IL-1β, IL-1RA, IL-6, IL-13, IP-10, and TNF with memory and only IL-1β with executive function), even controlling for age, sex, years of formal education, mood, and use of anti-inflammatory drugs. Regression analysis showed that several of these molecules (IL-1β, IL-6, IL-8, and IL-13) contribute to predicting whether an individual belongs to the "Good" or "Poor" cognitive performance group.
These results strengthen the hypothesis that increased concentrations of peripheral immune molecules, like IL-1β, are associated with worse cognitive performance in senior healthy individuals. It further highlights that some poorly studied immune molecules should be considered in the context of cognitive aging, such as IL-13, here revealed as a new player in such interaction.
老年人的认知能力存在异质性。免疫系统衰老越来越被认为是认知表现的潜在参与者。我们在这里探讨了健康老年人中认知表现与外周免疫分子之间的相互作用。
对临床特征明确的健康老年人(120 人;51-87 岁)进行横断面研究,这些老年人先前根据评估记忆和执行功能的既定测试聚类为“表现良好”和“表现不佳”。通过多重分析评估了 30 种免疫分子的血浆浓度,并将其与认知表现参数相关联。
与认知表现更好的个体(“表现良好”)相比,认知表现较差的个体(“表现不佳”)的 IL-1β、IL-8、IL-13 和肿瘤坏死因子(TNF)浓度增加。分别考虑记忆和执行功能这两个认知维度时,它们与几种免疫分子呈负相关(IL-1β、IL-1RA、IL-6、IL-13、IP-10 和 TNF 与记忆有关,而只有 IL-1β 与执行功能有关),即使控制了年龄、性别、受正规教育年限、情绪和使用抗炎药物等因素。回归分析显示,这些分子中的几种(IL-1β、IL-6、IL-8 和 IL-13)有助于预测个体属于“表现良好”还是“表现不佳”认知表现组。
这些结果加强了这样一种假设,即外周免疫分子(如 IL-1β)浓度增加与健康老年人认知表现较差有关。它进一步强调,在认知衰老的背景下,应考虑一些研究较少的免疫分子,如 IL-13,这是该相互作用中的一个新参与者。