Di Gerlando Rosalinda, Dragoni Francesca, Rizzo Bartolo, Ferrari Riccardo Rocco, Zardini Elisabetta, Ramusino Matteo Cotta, Perini Giulia, Costa Alfredo, Poloni Tino Emanuele, Pansarasa Orietta, Davin Annalisa, Gagliardi Stella
Department of Biology and Biotechnology "L. Spallanzani", University of Pavia, 27100 Pavia, Italy.
Molecular Biology and Transcriptomics Unit, IRCCS Mondino Foundation, 27100 Pavia, Italy.
Aging Dis. 2024 Jun 24;16(3):1639-1651. doi: 10.14336/AD.2024.0350.
APOE ɛ4 allele is the major genetic risk factor for Alzheimer's Disease (AD). Furthermore, APOE methylation pattern has been described to be associated with the disease and to follow a bimodal pattern, with a hypermethylated CpG island and a hypomethylated promoter region. However, little is known about the methylation levels in the APOE 5'UTR region. Here, the methylation of two regions (R1 and R2) within APOE 5'UTR was investigated in both peripheral blood mononuclear cells (PBMCs) and hippocampus (HIC) samples to identify differentially methylated CpG sites and to associate clinical, genetic features and cerebrospinal fluid (CSF) biomarkers levels. DNA was extracted from PBMCs of 20 AD and 20 healthy controls (HC) and from 6 AD and 3 HC HIC samples. The methylation analysis was carried out by means of pyrosequencing. In AD PBMCs we found that R1 region displayed a higher methylation level, while the opposite trend was observed in R2. The presence of ɛ4 allele highlighted a marked increase in R1 methylation level and a decrease in R2. In AD PBMCs and HIC, age progression resulted to be associated with an increase in the methylation level of R1. Lastly, the methylation of a CpG site in R2 was found to be related to CSF biomarkers. Despite the lack of a statistical significance, the outcome from this exploratory analysis highlighted the presence of a difference in methylation in APOE 5'UTR in PBMCs of AD patients which seemed to be associated also with APOE genotype, age and CSF biomarkers level.
APOE ε4等位基因是阿尔茨海默病(AD)的主要遗传风险因素。此外,已有研究表明APOE甲基化模式与该疾病相关,并呈双峰模式,即一个CpG岛高甲基化而启动子区域低甲基化。然而,关于APOE 5'非翻译区(UTR)的甲基化水平却知之甚少。在此,我们对外周血单核细胞(PBMCs)和海马体(HIC)样本中APOE 5'UTR内的两个区域(R1和R2)进行了甲基化研究,以确定差异甲基化的CpG位点,并将其与临床、遗传特征及脑脊液(CSF)生物标志物水平相关联。从20例AD患者和20例健康对照(HC)的PBMCs以及6例AD患者和3例HC的HIC样本中提取DNA。通过焦磷酸测序进行甲基化分析。在AD患者的PBMCs中,我们发现R1区域显示出较高的甲基化水平,而R2区域则呈现相反的趋势。ε4等位基因的存在突出表明R1甲基化水平显著升高而R2甲基化水平降低。在AD患者的PBMCs和HIC中,年龄增长与R1甲基化水平的升高相关。最后,发现R2中一个CpG位点的甲基化与CSF生物标志物有关。尽管缺乏统计学意义,但这项探索性分析的结果突出显示AD患者PBMCs中APOE 5'UTR的甲基化存在差异,这似乎也与APOE基因型、年龄和CSF生物标志物水平相关。