Individual differences in associative memory among older adults explained by hippocampal subfield structure and function

被引:53
|
作者
Carr, Valerie A. [1 ]
Bernstein, Jeffrey D. [2 ]
Favila, Serra E. [1 ]
Rutt, Brian K. [3 ]
Kerchner, Geoffrey A. [2 ]
Wagner, Anthony D. [1 ,4 ]
机构
[1] Stanford Univ, Dept Psychol, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Neurol & Neurol Sci, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Radiol, Stanford, CA 94305 USA
[4] Stanford Univ, Stanford Neurosci Inst, Stanford, CA 94305 USA
关键词
episodic memory; hippocampus; aging; mild cognitive impairment; Alzheimer's disease; MEDIAL TEMPORAL-LOBE; MILD COGNITIVE IMPAIRMENT; APICAL NEUROPIL ATROPHY; ALZHEIMERS-DISEASE; ENTORHINAL CORTEX; MRI MEASURES; AGE; CA1; DECLINE; NEURODEGENERATION;
D O I
10.1073/pnas.1713308114
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Older adults experience impairments in episodic memory, ranging from mild to clinically significant. Given the critical role of the medial temporal lobe (MTL) in episodic memory, age-related changes in MTL structure and function may partially account for individual differences in memory. Using ultra-high-field 7T structural MRI and high-resolution 3T functional MRI (hr-fMRI), we evaluated MTL subfield thickness and function in older adults representing a spectrum of cognitive health. Participants performed an associative memory task during hr-fMRI in which they encoded and later retrieved face-name pairs. Motivated by prior research, we hypothesized that differences in performance would be explained by the following: (i) entorhinal cortex (ERC) and CA1 apical neuropil layer [CA1-stratum radiatum lacunosum moleculare (SRLM)] thickness, and (ii) activity in ERC and the dentate gyrus (DG)/CA3 region. Regression analyses revealed that this combination of factors significantly accounted for variability in memory performance. Among these metrics, CA1-SRLM thickness was positively associated with memory, whereas DG/CA3 retrieval activity was negatively associated with memory. Furthermore, including structural and functional metrics in the same model better accounted for performance than did single-modality models. These results advance the understanding of how independent but converging influences of both MTL subfield structure and function contribute to age-related memory impairment, complementing findings in the rodent and human postmortem literatures.
引用
收藏
页码:12075 / 12080
页数:6
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