Medical College of Wisconsin
CTSICores SearchResearch InformaticsREDCap

Five-Year Longitudinal Brain Volume Change in Healthy Elders at Genetic Risk for Alzheimer's Disease. J Alzheimers Dis 2017;55(4):1363-1377

Date

11/12/2016

Pubmed ID

27834774

Pubmed Central ID

PMC5924681

DOI

10.3233/JAD-160504

Scopus ID

2-s2.0-85007275582 (requires institutional sign-in at Scopus site)   34 Citations

Abstract

Neuropathological changes associated with Alzheimer's disease (AD) precede symptom onset by more than a decade. Possession of an apolipoprotein E (APOE) ɛ4 allele is the strongest genetic risk factor for late onset AD. Cross-sectional studies of cognitively intact elders have noted smaller hippocampal/medial temporal volumes in ɛ4 carriers (ɛ4+) compared to ɛ4 non-carriers (ɛ4-). Few studies, however, have examined long-term, longitudinal, anatomical brain changes comparing healthy ɛ4+ and ɛ4- individuals. The current five-year study examined global and regional volumes of cortical and subcortical grey and white matter and ventricular size in 42 ɛ4+ and 30 ɛ4- individuals. Cognitively intact participants, ages 65-85 at study entry, underwent repeat anatomical MRI scans on three occasions: baseline, 1.5, and 4.75 years. Results indicated no between-group volumetric differences at baseline. Over the follow-up interval, the ɛ4+ group experienced a greater rate of volume loss in total grey matter, bilateral hippocampi, right hippocampal subfields, bilateral lingual gyri, bilateral parahippocampal gyri, and right lateral orbitofrontal cortex compared to the ɛ4- group. Greater loss in grey matter volumes in ɛ4+ participants were accompanied by greater increases in lateral, third, and fourth ventricular volumes. Rate of change in white matter volumes did not differentiate the groups. The current results indicate that longitudinal measurements of brain atrophy can serve as a sensitive biomarker for identifying neuropathological changes in persons at genetic risk for AD and potentially, for assessing the efficacy of treatments designed to slow or prevent disease progression during the preclinical stage of AD.

Author List

Reiter K, Nielson KA, Durgerian S, Woodard JL, Smith JC, Seidenberg M, Kelly DA, Rao SM

Author

Kristy Nielson PhD Professor in the Psychology department at Marquette University




MESH terms used to index this publication - Major topics in bold

Aged
Aged, 80 and over
Aging
Alzheimer Disease
Apolipoprotein E4
Atrophy
Brain
Cognition Disorders
Female
Functional Laterality
Humans
Image Processing, Computer-Assisted
Lateral Ventricles
Longitudinal Studies
Magnetic Resonance Imaging
Male
Mental Status Schedule
Middle Aged
Statistics as Topic