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老年人进展性痴呆的血液 DNA 甲基化模式。

Blood DNA Methylation Patterns in Older Adults With Evolving Dementia.

机构信息

Cancer Epigenetics and Nanomedicine Laboratory, Nanomaterials and Nanotechnology Research Center (CINN-CSIC), El Entrego, Spain.

Health Research Institute of Asturias (ISPA-FINBA), University of Oviedo, Oviedo, Spain.

出版信息

J Gerontol A Biol Sci Med Sci. 2022 Sep 1;77(9):1743-1749. doi: 10.1093/gerona/glac068.

Abstract

Dementia and cognitive disorders are major aging-associated pathologies. The prevalence and severity of these conditions are influenced by both genetic and environmental factors. Reflecting this, epigenetic alterations have been associated with each of these processes, especially at the level of DNA methylation, and such changes may help explain the observed interindividual variability in the development of the 2 pathologies. However, the importance of epigenetic alterations in explaining their etiology is unclear because little is known about the timing of when they appear. Here, using Illumina MethylationEPIC arrays, we have longitudinally analyzed the peripheral blood methylomes of cognitively healthy older adults (>70 year), some of whom went on to develop dementia while others stayed healthy. We have characterized 34 individuals at the prediagnosis stage and at a 4-year follow-up in the postdiagnosis stage (total n = 68). Our results show multiple DNA methylation alterations linked to dementia status, particularly at the level of differentially methylated regions. These loci are associated with several dementia-related genes, including PON1, AP2A2, MAGI2, POT1, ITGAX, PACSIN1, SLC2A8, and EIF4E. We also provide validation of the previously reported epigenetic alteration of HOXB6 and PM20D1. Importantly, we show that most of these regions are already altered in the prediagnosis stage of individuals who go on to develop dementia. In conclusion, our observations suggest that dementia-associated epigenetic patterns that have specific biological features are already present before diagnosis, and thus may be important in the design of epigenetic biomarkers for disease detection based on peripheral tissues.

摘要

痴呆和认知障碍是主要的与衰老相关的病理。这些疾病的患病率和严重程度受到遗传和环境因素的影响。反映这一点,表观遗传改变与这些过程中的每一个过程都有关联,尤其是在 DNA 甲基化水平上,这些变化可能有助于解释观察到的两种病理发展的个体间变异性。然而,由于对它们出现的时间知之甚少,因此表观遗传改变在解释其病因学中的重要性尚不清楚。在这里,我们使用 Illumina MethylationEPIC 阵列,对认知健康的老年人(>70 岁)的外周血甲基组进行了纵向分析,其中一些人后来发展为痴呆,而另一些人保持健康。我们在诊断前阶段和诊断后 4 年的随访阶段对 34 个人进行了特征描述(总共 n = 68)。我们的结果显示,与痴呆状态相关的多个 DNA 甲基化改变,特别是在差异甲基化区域水平上。这些基因座与几种与痴呆相关的基因有关,包括 PON1、AP2A2、MAGI2、POT1、ITGAX、PACSIN1、SLC2A8 和 EIF4E。我们还提供了先前报道的 HOXB6 和 PM20D1 表观遗传改变的验证。重要的是,我们表明,在发展为痴呆的个体的诊断前阶段,大多数这些区域已经发生改变。总之,我们的观察结果表明,与痴呆相关的具有特定生物学特征的表观遗传模式在诊断前就已经存在,因此可能对基于外周组织的疾病检测的表观遗传生物标志物的设计很重要。

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