Sudheimer Keith D, O'Hara Ruth, Spiegel David, Powers Bevin, Kraemer Helena C, Neri Eric, Weiner Michael, Hardan Antonio, Hallmayer Joachim, Dhabhar Firdaus S
Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford University Stanford, CA, USA.
Department of Radiology, University of California San Francisco, CA, USA ; Department of Veterans Affairs Medical Center, Center for Imaging of Neurodegenerative Diseases San Francisco, CA, USA.
Front Aging Neurosci. 2014 Jul 3;6:153. doi: 10.3389/fnagi.2014.00153. eCollection 2014.
Separate bodies of literature report that elevated pro-inflammatory cytokines and cortisol negatively affect hippocampal structure and cognitive functioning, particularly in older adults. Although interactions between cytokines and cortisol occur through a variety of known mechanisms, few studies consider how their interactions affect brain structure. In this preliminary study, we assess the impact of interactions between circulating levels of IL-1Beta, IL-6, IL-8, IL-10, IL-12, TNF-alpha, and waking cortisol on hippocampal volume. Twenty-eight community-dwelling older adults underwent blood draws for quantification of circulating cytokines and saliva collections to quantify the cortisol awakening response. Hippocampal volume measurements were made using structural magnetic resonance imaging. Elevated levels of waking cortisol in conjunction with higher concentrations of IL-6 and TNF-alpha were associated with smaller hippocampal volumes. In addition, independent of cortisol, higher levels of IL-1beta and TNF-alpha were also associated with smaller hippocampal volumes. These data provide preliminary evidence that higher cortisol, in conjunction with higher IL-6 and TNF-alpha, are associated with smaller hippocampal volume in older adults. We suggest that the dynamic balance between the hypothalamic-pituitary adrenal axis and inflammation processes may explain hippocampal volume reductions in older adults better than either set of measures do in isolation.
不同的文献报道称,促炎细胞因子和皮质醇水平升高会对海马体结构和认知功能产生负面影响,尤其是在老年人中。尽管细胞因子和皮质醇之间的相互作用通过多种已知机制发生,但很少有研究考虑它们的相互作用如何影响脑结构。在这项初步研究中,我们评估了循环中的白细胞介素-1β、白细胞介素-6、白细胞介素-8、白细胞介素-10、白细胞介素-12、肿瘤坏死因子-α水平与清醒时的皮质醇之间的相互作用对海马体体积的影响。28名居住在社区的老年人接受了血液抽取以量化循环细胞因子,并收集唾液以量化皮质醇觉醒反应。使用结构磁共振成像进行海马体体积测量。清醒时皮质醇水平升高,同时白细胞介素-6和肿瘤坏死因子-α浓度较高,与较小的海马体体积相关。此外,独立于皮质醇,白细胞介素-1β和肿瘤坏死因子-α水平较高也与较小的海马体体积相关。这些数据提供了初步证据,表明较高的皮质醇,连同较高的白细胞介素-6和肿瘤坏死因子-α,与老年人较小的海马体体积相关。我们认为,下丘脑-垂体-肾上腺轴与炎症过程之间的动态平衡可能比单独的任何一组测量更能解释老年人海马体体积的减少。