Department of Medicine and Aging Sciences, University "G. d'Annunzio", Chieti, Italy.
Department of Neuroscience, Catholic University of Sacred Heart, Rome, Italy.
J Alzheimers Dis. 2024;99(3):1147-1158. doi: 10.3233/JAD-231471.
Neuroinflammation, with altered peripheral proinflammatory cytokine production, plays a major role in the pathogenesis of neurodegenerative diseases, such as Alzheimer's disease (AD), while the role of inflammation in dementia with Lewy bodies (DLB) is less known and the results of different studies are often in disagreement.
The present study aimed to investigate the levels of TNFα and IL-6 in serum and supernatants, and the related DNA methylation in patients affected by DLB and AD compared to healthy controls (HCs), to clarify the role of epigenetic mechanisms of DNA promoter methylation on of pro-inflammatory cytokines overproduction.
Twenty-one patients with DLB and fourteen with AD were frequency-matched for age and sex with eleven HCs. Clinical evaluation, TNFα and IL-6 gene methylation status, cytokine gene expression levels and production in serum and peripheral blood mononuclear cell (PBMC) supernatants were performed.
In AD and DLB patients, higher serum levels of IL-6 and TNFα were detected than in HCs. Differences in LPS-stimulated versus spontaneous PBMCs were observed between DLB, AD, and HC in the levels of TNFα (p = 0.027) and IL-6 (p < 0.001). Higher levels were also revealed for sIL-6R in DLB (p < 0.001) and AD (p < 0.001) in comparison with HC.DNA hypomethylation in IL-6 and TNFα CpG promoter sites was detected for DLB and AD patients compared to the corresponding site in HCs.
Our preliminary study documented increased levels of IL-6 and TNFα in DLB and AD patients to HCs. This overproduction can be due to epigenetic mechanisms regarding the hypomethylation of DNA promoters.
神经炎症通过改变外周促炎细胞因子的产生,在神经退行性疾病(如阿尔茨海默病)的发病机制中发挥重要作用,而炎症在路易体痴呆(DLB)中的作用知之甚少,不同研究的结果往往存在分歧。
本研究旨在比较 DLB 和 AD 患者与健康对照者(HC)血清和上清液中 TNFα 和 IL-6 的水平以及相关 DNA 甲基化,以阐明 DNA 启动子甲基化的表观遗传机制在促炎细胞因子过度产生中的作用。
对 21 例 DLB 患者和 14 例 AD 患者进行年龄和性别频率匹配,共 11 例 HC。进行临床评估、TNFα 和 IL-6 基因甲基化状态、细胞因子基因表达水平以及血清和外周血单个核细胞(PBMC)上清液中的产生。
与 HC 相比,AD 和 DLB 患者血清中 IL-6 和 TNFα 水平升高。与 HC 相比,在 LPS 刺激和自发 PBMC 中,DLB、AD 和 HC 之间 TNFα(p=0.027)和 IL-6(p<0.001)的水平存在差异。与 HC 相比,DLB(p<0.001)和 AD(p<0.001)中 sIL-6R 的水平也更高。与相应的 HC 相比,DLB 和 AD 患者的 IL-6 和 TNFα CpG 启动子位点的 DNA 低甲基化。
我们的初步研究记录了 DLB 和 AD 患者中 IL-6 和 TNFα 水平高于 HC。这种过度产生可能归因于 DNA 启动子低甲基化的表观遗传机制。