Institute of Neuroscience, Campus for Ageing and Vitality,Newcastle University,Newcastle upon Tyne,UK.
Department of Psychiatry,University of Cambridge,Cambridge,UK.
Int Psychogeriatr. 2019 Apr;31(4):551-560. doi: 10.1017/S1041610218001126. Epub 2019 Mar 11.
ABSTRACTObjectives and design:To Investigate the peripheral inflammatory profile in patients with mild cognitive impairment (MCI) from three subgroups - probable Lewy body disease (probable MCI-LB), possible Lewy body disease, and probable Alzheimer's disease (probable MCI-AD) - as well as associations with clinical features.
Memory clinics and dementia services.
Patients were classified based on clinical symptoms as probable MCI-LB (n = 38), possible MCI-LB (n = 18), and probable MCI-AD (n = 21). Healthy comparison subjects were recruited (n = 20).
Ten cytokines were analyzed from plasma samples: interferon (IFN)-gamma, interleukin (IL)-1beta, IL-2, IL-4, IL-6, IL-8, IL-10, IL-12p70, IL-13, and tumor necrosis factor (TNF)-alpha. C-reactive protein levels were investigated.
There was a higher level of IL-10, IL-1beta, IL-2, and IL-4 in MCI groups compared to the healthy comparison group (p < 0.0085). In exploratory analyses to understand these findings, the MC-AD group lower IL-1beta (p = 0.04), IL-2 (p = 0.009), and IL-4 (p = 0.012) were associated with increasing duration of memory symptoms, and in the probable MCI-LB group, lower levels of IL-1beta were associated with worsening motor severity (p = 0.002). In the possible MCI-LB, longer duration of memory symptoms was associated with lower levels of IL-1beta (p = 0.003) and IL-4 (p = 0.026).
There is increased peripheral inflammation in patients with MCI compared to healthy comparison subjects regardless of the MCI subtype. These possible associations with clinical features are consistent with other work showing that inflammation is increased in early disease but require replication. Such findings have importance for timing of putative therapeutic strategies aimed at lowering inflammation.
调查轻度认知障碍(MCI)患者的外周炎症特征,这些患者来自三个亚组:可能的路易体病(可能的 MCI-LB)、可能的路易体病和可能的阿尔茨海默病(可能的 MCI-AD),以及与临床特征的关联。
记忆诊所和痴呆症服务机构。
根据临床症状,将患者分为可能的 MCI-LB(n = 38)、可能的 MCI-LB(n = 18)和可能的 MCI-AD(n = 21)。招募了健康对照组(n = 20)。
从血浆样本中分析了十种细胞因子:干扰素(IFN)-γ、白细胞介素(IL)-1β、IL-2、IL-4、IL-6、IL-8、IL-10、IL-12p70、IL-13 和肿瘤坏死因子(TNF)-α。还研究了 C 反应蛋白水平。
与健康对照组相比,MCI 组的 IL-10、IL-1β、IL-2 和 IL-4 水平更高(p < 0.0085)。在探索性分析中,为了理解这些发现,MCI-AD 组的 IL-1β(p = 0.04)、IL-2(p = 0.009)和 IL-4(p = 0.012)随着记忆症状持续时间的增加而降低,而在可能的 MCI-LB 组中,IL-1β 水平的降低与运动严重程度的恶化有关(p = 0.002)。在可能的 MCI-LB 中,记忆症状持续时间较长与 IL-1β(p = 0.003)和 IL-4(p = 0.026)水平降低有关。
与健康对照组相比,MCI 患者的外周炎症增加,无论 MCI 亚型如何。这些与临床特征的可能关联与其他表明炎症在早期疾病中增加的工作一致,但需要复制。这些发现对于确定针对降低炎症的潜在治疗策略的时间具有重要意义。