A Novel Computational Proxy for Characterizing Cognitive Reserve in Alzheimer’s Disease

Abstract

Background: Although the abnormal depositions of amyloid plaques and neurofibrillary tangles are the hallmark of Alzheimer’s disease (AD), converging evidence shows that the individual’s neurodegeneration trajectory is regulated by the brain’s capability to maintain normal cognition. Objective: The concept of cognitive reserve has been introduced into the field of neuroscience, acting as a moderating factor for explaining the paradoxical relationship between the burden of AD pathology and the clinical outcome. It is of high demand to quantify the degree of conceptual cognitive reserve on an individual basis. Methods: We propose a novel statistical model to quantify an individual’s cognitive reserve against neuropathological burdens, where the predictors include demographic data (such as age and gender), socioeconomic factors (such as education and occupation), cerebrospinal fluid biomarkers, and AD-related polygenetic risk score. We conceptualize cognitive reserve as a joint product of AD pathology and socioeconomic factors where their interaction manifests a significant role in counteracting the progression of AD in our statistical model. Results: We apply our statistical models to re-investigate the moderated neurodegeneration trajectory by considering cognitive reserve, where we have discovered that 1) high education individuals have significantly higher reserve against the neuropathology than the low education group; however, 2) the cognitive decline in the high education group is significantly faster than low education individuals after the level of pathological burden increases beyond the tipping point. Conclusion: We propose a computational proxy of cognitive reserve that can be used in clinical routine to assess the progression of AD.