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加速的表观遗传衰老及其在青年期脑动力学和认知中的作用。

Accelerated Epigenetic Aging and Its Role in Brain Dynamics and Cognition in Young Adulthood.

作者信息

Jordánek Tomáš, Mareček Radek, Pačínková Anna, Andrýsková Lenka, Brázdil Milan, Marečková Klára

机构信息

Brain and Mind Research, Central European Institute of Technology, Masaryk University (CEITEC MU), Brno, Czech Republic.

First Department of Neurology, St. Anne's University Hospital and Faculty of Medicine, Masaryk University, Brno, Czech Republic.

出版信息

Hum Brain Mapp. 2025 Jul;46(10):e70261. doi: 10.1002/hbm.70261.

Abstract

Accelerated epigenetic aging has been associated with changes in cognition. However, due to the lack of neuroimaging epigenetics studies, it is still unclear whether accelerated epigenetic. Aging in young adulthood might underlie the relationship between altered brain dynamics and cognitive functioning. We conducted neuroimaging epigenetics follow-up of the European Longitudinal Study of Pregnancy and Childhood (ELSPAC) prenatal birth cohort in young adulthood and tested the possible mediatory role of accelerated epigenetic aging in the relationship between dynamic functional connectivity (DFC) and worse cognition. A total of 240 young adults (51% men; 28-30 years, all of European ancestry) participated in the neuroimaging epigenetics follow-up. Buccal swabs were collected to assess DNA methylation and calculate epigenetic aging using Horvath's epigenetic clock. Full-scale IQ was assessed using the Wechsler adult intelligence scale (WAIS). Resting-state functional magnetic resonance imaging (rs-fMRI) was acquired using a 3T Siemens Prisma MRI scanner, and DFC was assessed using mixture factor analysis, revealing information about the coverage of different DFC states. In women (but not men), lower coverage of DFC state 4 and thus lower frequency of epochs with high connectivity within the default mode network and between default mode, fronto-parietal, and visual networks was associated with lower full-scale IQ (AdjR = 0.05, std. beta = 0.245, p = 0.008). This relationship was mediated by accelerated epigenetic aging (ab = 7.660, SE = 4.829, 95% CI [0.473, 19.264]). In women, accelerated epigenetic aging in young adulthood mediates the relationship between altered brain dynamics and cognitive functioning. Prevention of cognitive decline should target women already in young adulthood.

摘要

表观遗传加速衰老与认知变化有关。然而,由于缺乏神经影像学表观遗传学研究,目前仍不清楚青年期表观遗传加速衰老是否可能是大脑动态变化与认知功能之间关系的基础。我们对欧洲孕期和儿童纵向研究(ELSPAC)出生队列中的青年进行了神经影像学表观遗传学随访,并测试了表观遗传加速衰老在动态功能连接(DFC)与较差认知之间关系中可能的中介作用。共有240名青年(51%为男性;年龄28 - 30岁,均为欧洲血统)参与了神经影像学表观遗传学随访。采集颊拭子以评估DNA甲基化,并使用霍瓦斯表观遗传时钟计算表观遗传衰老。使用韦氏成人智力量表(WAIS)评估全量表智商。使用3T西门子Prisma MRI扫描仪进行静息态功能磁共振成像(rs - fMRI),并使用混合因子分析评估DFC,以揭示不同DFC状态的覆盖信息。在女性(而非男性)中,DFC状态4的覆盖率较低,因此默认模式网络内以及默认模式、额顶叶和视觉网络之间高连接性时段的频率较低,这与较低的全量表智商相关(调整后R = 0.05,标准β = 0.245,p = 0.008)。这种关系由表观遗传加速衰老介导(ab = 7.660,标准误 = 4.829,95%置信区间[0.473, 19.264])。在女性中,青年期表观遗传加速衰老介导了大脑动态变化与认知功能之间的关系。预防认知衰退应针对已处于青年期女性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce0e/12199205/e85bff3a8cdd/HBM-46-e70261-g003.jpg

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