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作为淀粉样蛋白负担的函数,任务难度的 BOLD 调制在年龄上的差异。

Age differences in BOLD modulation to task difficulty as a function of amyloid burden.

机构信息

Center for Vital Longevity; Department of Psychology, School of Behavioral and Brain Sciences, University of Texas at Dallas, 1600 Viceroy Dr., Suite 800, Dallas, TX 75235, United States.

Department of Psychiatry, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390, United States.

出版信息

Cereb Cortex. 2024 Sep 3;34(9). doi: 10.1093/cercor/bhae357.


DOI:10.1093/cercor/bhae357
PMID:39227310
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11371418/
Abstract

Effective cognitive performance often requires the allocation of additional neural resources (i.e. blood-oxygen-level-dependent [BOLD] activation) as task demands increase, and this demand-related modulation is affected by amyloid-beta deposition and normal aging. The present study investigated these complex relationships between amyloid, modulation, and cognitive function (i.e. fluid ability). Participants from the Dallas Lifespan Brain Study (DLBS, n = 252, ages 50-89) completed a semantic judgment task during functional magnetic resonance imaging (fMRI) where the judgments differed in classification difficulty. Amyloid burden was assessed via positron emission tomography (PET) using 18F-florbetapir. A quadratic relationship between amyloid standardized value uptake ratios (SUVRs) and BOLD modulation was observed such that modulation was weaker in those with moderately elevated SUVRs (e.g. just reaching amyloid-positivity), whereas those with very high SUVRs (e.g. SUVR > 1.5) showed strong modulation. Greater modulation was related to better fluid ability, and this relationship was strongest in younger participants and those with lower amyloid burden. These results support the theory that effective demand-related modulation contributes to healthy cognitive aging, especially in the transition from middle age to older adulthood, whereas high modulation may be dysfunctional in those with substantial amyloid deposition.

摘要

有效的认知表现通常需要分配额外的神经资源(即血氧水平依赖 [BOLD] 激活),随着任务需求的增加,这种需求相关的调节受到淀粉样蛋白-β沉积和正常衰老的影响。本研究调查了淀粉样蛋白、调节和认知功能(即流体能力)之间的这些复杂关系。达拉斯寿命期脑研究(DLBS,n=252,年龄 50-89 岁)的参与者在功能磁共振成像(fMRI)期间完成了一项语义判断任务,其中判断在分类难度上有所不同。通过正电子发射断层扫描(PET)使用 18F-氟比他滨评估淀粉样蛋白负担。观察到淀粉样蛋白标准化摄取比值(SUVR)与 BOLD 调节之间的二次关系,即中度升高的 SUVR(例如刚刚达到淀粉样蛋白阳性)的调节较弱,而 SUVR 非常高的(例如 SUVR>1.5)显示出强烈的调节。更大的调节与更好的流体能力相关,这种关系在年轻参与者和淀粉样蛋白负担较低的参与者中最强。这些结果支持了这样一种理论,即有效的需求相关调节有助于健康的认知衰老,特别是从中年到老年的过渡,而在淀粉样蛋白大量沉积的情况下,高调节可能是功能失调的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db5a/11371418/1637649a95c7/bhae357f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db5a/11371418/5aadefd31e6c/bhae357f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db5a/11371418/61be7b604a24/bhae357f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db5a/11371418/08af50ab0b63/bhae357f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db5a/11371418/9536e1f25a28/bhae357f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db5a/11371418/1637649a95c7/bhae357f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db5a/11371418/5aadefd31e6c/bhae357f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db5a/11371418/61be7b604a24/bhae357f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db5a/11371418/08af50ab0b63/bhae357f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db5a/11371418/9536e1f25a28/bhae357f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db5a/11371418/1637649a95c7/bhae357f5.jpg

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Age differences in BOLD modulation to task difficulty as a function of amyloid burden.

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[2]
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[4]
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引用本文的文献

[1]
Validation of dementia-free status in the iranian brain imaging database using ADNI data: a transition point from middle age to older adulthood.

BMC Neurol. 2025-7-10

[2]
The Dallas Lifespan Brain Study: A Comprehensive Adult Lifespan Data Set of Brain and Cognitive Aging.

Sci Data. 2025-5-26

本文引用的文献

[1]
Unravelling the relationship between amyloid accumulation and brain network function in normal aging and very mild cognitive decline: a longitudinal analysis.

Brain Commun. 2022-11-2

[2]
Relationship of prefrontal brain lateralization to optimal cognitive function differs with age.

Neuroimage. 2022-12-1

[3]
Amyloid-driven disruption of default mode network connectivity in cognitively healthy individuals.

Brain Commun. 2021-9-6

[4]
Functional Brain Network Connectivity Patterns Associated With Normal Cognition at Old-Age, Local β-amyloid, Tau, and APOE4.

Front Aging Neurosci. 2020-3-9

[5]
Increased soluble amyloid-beta causes early aberrant brain network hypersynchronisation in a mature-onset mouse model of amyloidosis.

Acta Neuropathol Commun. 2019-11-14

[6]
Contributions of White Matter Connectivity and BOLD Modulation to Cognitive Aging: A Lifespan Structure-Function Association Study.

Cereb Cortex. 2020-3-14

[7]
Association Between Earliest Amyloid Uptake and Functional Connectivity in Cognitively Unimpaired Elderly.

Cereb Cortex. 2019-5-1

[8]
Regional amyloid accumulation and cognitive decline in initially amyloid-negative adults.

Neurology. 2018-10-10

[9]
Increasing beta-amyloid deposition in cognitively healthy aging predicts nonlinear change in BOLD modulation to difficulty.

Neuroimage. 2018-8-11

[10]
Age-related changes in the neural networks supporting semantic cognition: A meta-analysis of 47 functional neuroimaging studies.

Neurosci Biobehav Rev. 2017-11-26

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