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寿命记忆差异的多种决定因素。

Multiple determinants of lifespan memory differences.

机构信息

Medical Research Council, Cognition and Brain Sciences Unit, Cambridge, UK.

Cambridge Centre for Ageing and Neuroscience, University of Cambridge and MRC Cognition and Brain Sciences Unit, Cambridge, USA.

出版信息

Sci Rep. 2016 Sep 7;6:32527. doi: 10.1038/srep32527.

DOI:10.1038/srep32527
PMID:27600595
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5013267/
Abstract

Memory problems are among the most common complaints as people grow older. Using structural equation modeling of commensurate scores of anterograde memory from a large (N = 315), population-derived sample (www.cam-can.org), we provide evidence for three memory factors that are supported by distinct brain regions and show differential sensitivity to age. Associative memory and item memory are dramatically affected by age, even after adjusting for education level and fluid intelligence, whereas visual priming is not. Associative memory and item memory are differentially affected by emotional valence, and the age-related decline in associative memory is faster for negative than for positive or neutral stimuli. Gray-matter volume in the hippocampus, parahippocampus and fusiform cortex, and a white-matter index for the fornix, uncinate fasciculus and inferior longitudinal fasciculus, show differential contributions to the three memory factors. Together, these data demonstrate the extent to which differential ageing of the brain leads to differential patterns of memory loss.

摘要

随着年龄的增长,记忆问题是最常见的抱怨之一。我们使用来自大型(N=315)人群样本的顺行记忆相当分数的结构方程建模(www.cam-can.org),为三个记忆因素提供了证据,这些因素由不同的大脑区域支持,并对年龄表现出不同的敏感性。即使在调整了教育水平和流体智力后,联想记忆和项目记忆也会受到年龄的显著影响,而视觉启动则不会。联想记忆和项目记忆受情绪效价的影响不同,并且与正性或中性刺激相比,负性刺激的联想记忆的年龄相关性下降更快。海马体、旁海马体和梭状回的灰质体积,以及穹窿、钩束和下纵束的白质指数,对三个记忆因素有不同的贡献。总的来说,这些数据表明大脑的不同衰老程度导致了不同的记忆丧失模式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/032d/5013267/fae7c2fde38b/srep32527-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/032d/5013267/3f3e83b0dcb1/srep32527-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/032d/5013267/524284511a67/srep32527-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/032d/5013267/2b2ee151190b/srep32527-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/032d/5013267/d33fc1e7e9a7/srep32527-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/032d/5013267/fae7c2fde38b/srep32527-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/032d/5013267/3f3e83b0dcb1/srep32527-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/032d/5013267/524284511a67/srep32527-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/032d/5013267/2b2ee151190b/srep32527-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/032d/5013267/d33fc1e7e9a7/srep32527-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/032d/5013267/fae7c2fde38b/srep32527-f5.jpg

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Extent of hippocampal atrophy predicts degree of deficit in recall.
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Alcohol Use Disorder and Dementia: A Review.酒精使用障碍与痴呆:综述。
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