Can a Data-Driven Measure of Neuroanatomic Dementia Risk be Considered a Measure of Brain Aging?. (17th December 2021)

• Record Type: Journal Article
• Authors: Casanova, Ramon; Anderson, Andrea; Justice, Jamie; Windham, Gwen; Gottesman, Rebecca; Mosley, Thomas; Wagenknecht, Lynne; Kritchevsky, Stephen
• Is Part Of: Innovation in aging. Volume 5(2021)Supplement 1
• Page Start: 962
• Page End: 963
• Publication Date: 2021-12-17
• Subjects: Aging -- Periodicals; Gerontology -- Periodicals; 612.67
• DOI: 10.1093/geroni/igab046.3470
• Languages: English
• ISSNs: 2399-5300

Abstract

Abstract: There is an increasing interest in identifying aging-related factors which may be permissive of Alzheimer's Disease (AD) emergence. We previously used machine learning to derive an index of neuroanatomic risk of dementia called AD pattern similarity (AD-PS) score using MRIs obtained in the Atherosclerosis Risk in Communities (ARIC) study. Here, we investigate the potential of the AD-PS scores as a brain-focused measure of biologic age. Among 1970 ARIC participants with MRI collected at ARIC Visit 5, we related AD-PS scores to three measures of aging: mortality (n=356) over 8 years of follow-up; an a priori panel of 32 proteins related to aging (N=1647); and a deficit accumulation index (DAI) based on 38 health-related measures. We found lower AD-PS scores associated with significantly lower mortality (HR=0.58, CI-95%, [0.45 - 0.75], p < 0.001) after adjusting for age, race, smoking and hypertension. Among the 32 proteins, nine were significantly associated to AD-PS scores (p < 0.05) with 4 remaining significant adjusting for multiple comparisons (Growth/differentiation factor 15, Tumor necrosis factor receptor superfamily member 1A and 1B and Collagen alpha-1(XVIII) chain). Finally, in a linear regression model after adjusting for age, race, sex, hypertension and smoking, AD-PS scores were associated with the DAI (p < 0.001). The consistent patterns of associations suggest that a data-driven measure of AD neuroanatomic risk may be capturing aspects of biologic age in older adults.