Neurofibrillary Tangles and Conversion to Mild Cognitive Impairment with Certain Antihypertensives

• Type of Material: Article
• Authors: Whitney Wharton, Emory University; Liping Zhao, Emory University; Nelson Steenland, Emory University; Felicia Goldstein, Emory University; Julie A. Schneider, Rush University; Lisa L. Barnes, Rush University; Marla Gearing, Emory University; Sevil Yasar, Johns Hopkins University
• Language: English
• Date: 2019-01-01
• Publisher: IOS Press
• Publication Version: Author Accepted Manuscript (After Peer Review)
• Copyright Statement: © 2019 IOS Press.
• Final Published Version (URL): http://dx.doi.org/10.3233/JAD-190011
• Title of Journal or Parent Work: Journal of Alzheimers Disease
• Volume: 70
• Issue: 1
• Start Page: 153
• End Page: 161
• Grant/Funding Information: This work was supported by the Emory and Rush Alzheimer’s Disease Research Centers (NIH-NIA 5 P50 AG025688, P30AG10161) and National Institute on Aging (K01AG042498, R13AG030995, R01AG017917).
• Keywords: Life Sciences & Biomedicine; Older adults; tau; Disease; ACE inhibitors; neuropathology; mild cognitive impairment; National institute; blood pressure; Science & Technology; Alzheimers association workgroups; Neurosciences & Neurology; Dementia; Decline; renin angiotensin system; Neurosciences; hypertension; Diagnostic guidelines; Alzheimer's disease; prevention; Receptor blockers
• Research Categories: Biology, Biostatistics; Health Sciences, Pathology; Biology, Neuroscience; Biology, Bioinformatics

Abstract

Background: Individuals taking renin angiotensin system (RAS) acting antihypertensives exhibit slower cognitive decline and are less likely to progress from mild cognitive impairment (MCI) to Alzheimer’s disease (AD), but the mechanism remains unclear. Objective: We tested the hypothesis that individuals taking RAS acting antihypertensives exhibit less AD-related neuropathology and slower disease progression than individuals taking non-RAS acting antihypertensives. Method: Participants included 83 individuals with MCI who were taking an antihypertensive at baseline, had at least two follow-up visits, and had postmortem neuropathological data. Participants were old (M = 83.1 years), 32% male, well educated (M = 15.7 years), and 9.2% Black. Results: RAS medication users (N = 38) were less likely to progress to AD than non-RAS users (N = 45). RAS users exhibited fewer neurofibrillary tangles than non-RAS users in the hippocampal CA1 region (p < 0.01), entorhinal cortex (p = 0.03), and the angular gyrus, inferior temporal, mid-frontal cortex, and superior frontal (p = 0.01). Conclusion: Prevention or clearance of neurofibrillary tangles represents a mechanism by which RAS medications may slow disease progression.