Ningbo Key Laboratory of Behavioral Neuroscience, Zhejiang Provincial Key Laboratory of Pathophysiology, School of Medicine, Ningbo University, Ningbo, Zhejiang 315211, P.R. China.
Department of Science and Education, Ningbo No. 9 Hospital, Ningbo, Zhejiang 315010, P.R. China.
Mol Med Rep. 2018 Nov;18(5):4297-4302. doi: 10.3892/mmr.2018.9424. Epub 2018 Aug 24.
Previous studies have suggested that increased opioid receptor κ1 (OPRK1) and opioid receptor δ1 (OPRD1) methylation levels are involved in Alzheimer's disease (AD). In the present study, the methylation levels of two opioid receptor genes, opioid receptor µ1 (OPRM1) and opioid related nociceptin receptor 1 (OPRL1), were analyzed for their association with AD. Gene methylation levels were measured using bisulfite pyrosequencing in DNA samples derived from blood samples of 51 AD patients and 63 controls. The results indicated that there were significantly elevated promoter methylation levels of OPRM1 and OPRL1 in AD (OPRM1: P=0.007; OPRL1: P=2.987x10‑6). Dual‑luciferase reporter gene assays demonstrated that the promoter fragments of these two genes were able to promote gene expression (OPRM1: Fold‑change=2.616, P=0.003; OPRL1: Fold change=11.395, P=0.007). In addition, receiver operating characteristic analyses further indicated that a methylation panel of four opioid receptor genes (area under the curve=0.848, sensitivity=0.723, and specificity=0.879) performed well in the prediction of AD. These results suggested that opioid receptor genes may be used as potential methylation biomarkers for the diagnosis of AD.
先前的研究表明,阿片受体 κ1(OPRK1)和阿片受体 δ1(OPRD1)的甲基化水平升高与阿尔茨海默病(AD)有关。在本研究中,分析了两种阿片受体基因,阿片受体 μ1(OPRM1)和阿片相关的痛敏受体 1(OPRL1)的甲基化水平与 AD 的相关性。通过对来自 51 例 AD 患者和 63 例对照者血液样本的 DNA 样本进行亚硫酸氢盐焦磷酸测序,测量了基因的甲基化水平。结果表明,AD 患者的 OPRM1 和 OPRL1 启动子甲基化水平显著升高(OPRM1:P=0.007;OPRL1:P=2.987x10-6)。双荧光素酶报告基因检测表明,这两个基因的启动子片段能够促进基因表达(OPRM1:Fold-change=2.616,P=0.003;OPRL1:Fold change=11.395,P=0.007)。此外,受试者工作特征分析进一步表明,四个阿片受体基因的甲基化谱(曲线下面积=0.848,敏感性=0.723,特异性=0.879)在 AD 的预测中表现良好。这些结果表明,阿片受体基因可能作为 AD 诊断的潜在甲基化生物标志物。