Abstract

Individuals with subjective cognitive decline (SCD) are at high risk of developing preclinical or clinical state of Alzheimer’s disease (AD). Resting state functional magnetic resonance imaging, which can indirectly reflect neuron activities by measuring the blood-oxygen-level-dependent (BOLD) signals, is promising in the early detection of SCD. This study aimed to explore whether the nonlinear complexity of BOLD signals can describe the subtle differences between SCD and normal aging, and uncover the underlying neuropsychological implications of these differences. In particular, we introduce amplitude-aware permutation entropy (AAPE) as the novel measure of brain entropy to characterize the complexity in BOLD signals in each brain region of the Brainnetome atlas. Our results demonstrate that AAPE can reflect the subtle differences between both groups, and the SCD group presented significantly decreased complexities in subregions of the superior temporal gyrus, the inferior parietal lobule, the postcentral gyrus, and the insular gyrus. Moreover, the results further reveal that lower complexity in SCD may correspond to poorer cognitive performance or even subtle cognitive impairment. Our findings demonstrated the effectiveness and sensitiveness of the novel brain entropy measured by AAPE, which may serve as the potential neuroimaging marker for exploring the subtle changes in SCD.

Highlights

  • Program of Jiangsu Province of China.Institutional Review Board Statement: The study was conducted according to the guidelines of the Declaration of Helsinki, and approved by the Institutional Review Board of the Alzheimer’s Disease Neuroimaging Initiative (ADNI) (National Institutes of Health Grant U01 AG024904).Informed Consent Statement: Informed consent was obtained from all subjects involved in the study

  • aware permutation entropy (AAPE) values of the subjective cognitive decline (SCD) group were relatively lower than those of the normal aging (NA) group for all of the eight regions of interests (ROI). These ROIs included the subregions of the bilateral superior temporal gyrus (STG) (A41/42.L, TE.L, TE.R and A22r.R), the rostroventral areas of the bilateral inferior parietal lobule (IPL) (A40rv.L and A40rv.R), the tongue and larynx region of the right postcentral gyrus (PoG) (A1/2/3tonIa.R) and the dorsal granular insula of the right insular gyrus (INS)

  • This study introduced AAPE as the novel measure of brain entropy to investigate the intergroup differences in complexity between NA and SCD

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Summary

Objectives

This study aimed to explore whether the nonlinear complexity of BOLD signals can describe the subtle differences between SCD and normal aging, and uncover the underlying neuropsychological implications of these differences.

Methods
Results
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Conclusion

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