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中老年大脑形态的年龄相关性差异及其调节因素。

Age-Related Differences in Brain Morphology and the Modifiers in Middle-Aged and Older Adults.

机构信息

Laboratory of Neuro Imaging, USC Mark and Mary Stevens Neuroimaging and Informatics Institute, University of Southern California, Los Angeles, CA 90033, USA.

Statistics Online Computational Resource, HBBS, University of Michigan, Ann Arbor, MI 48109-2003, USA.

出版信息

Cereb Cortex. 2019 Sep 13;29(10):4169-4193. doi: 10.1093/cercor/bhy300.

Abstract

Brain structural morphology differs with age. This study examined age-differences in surface-based morphometric measures of cortical thickness, volume, and surface area in a well-defined sample of 8137 generally healthy UK Biobank participants aged 45-79 years. We illustrate that the complexity of age-related brain morphological differences may be related to the laminar organization and regional evolutionary history of the cortex, and age of about 60 is a break point for increasing negative associations between age and brain morphology in Alzheimer's disease (AD)-prone areas. We also report novel relationships of age-related cortical differences with individual factors of sex, cognitive functions of fluid intelligence, reaction time and prospective memory, cigarette smoking, alcohol consumption, sleep disruption, genetic markers of apolipoprotein E, brain-derived neurotrophic factor, catechol-O-methyltransferase, and several genome-wide association study loci for AD and further reveal joint effects of cognitive functions, lifestyle behaviors, and education on age-related cortical differences. These findings provide one of the most extensive characterizations of age associations with major brain morphological measures and improve our understanding of normal structural brain aging and its potential modifiers.

摘要

大脑结构形态随年龄而变化。本研究在一个明确的、由 8137 名年龄在 45-79 岁的、通常健康的英国生物银行参与者组成的样本中,考察了皮质厚度、体积和表面积的基于表面的形态测量指标的年龄差异。我们表明,与年龄相关的大脑形态差异的复杂性可能与皮质的层状组织和区域进化历史有关,大约 60 岁是阿尔茨海默病(AD)易感区域中年龄与大脑形态之间负相关关系增加的转折点。我们还报告了与个体因素(性别、流体智力认知功能、反应时间和前瞻性记忆)、吸烟、饮酒、睡眠障碍、载脂蛋白 E、脑源性神经营养因子、儿茶酚-O-甲基转移酶的遗传标志物以及几个与 AD 相关的全基因组关联研究位点相关的皮质差异的新关系,并进一步揭示了认知功能、生活方式行为和教育对与年龄相关的皮质差异的联合影响。这些发现提供了与大脑主要形态测量指标的年龄相关性的最广泛描述之一,提高了我们对正常结构大脑老化及其潜在修饰物的理解。

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