<i>APOE</i> ε4–associated heterogeneity of neuroimaging biomarkers across the Alzheimer's disease continuum

An extensive study was performed on the apolipoprotein E (APOE) ε4-associated heterogeneity in neuroimaging biomarkers from the Alzheimer's Disease Neuroimaging Initiative. Robust APOE ε4-associated increases in amyloid beta (Aβ) deposition throughout the brain, in every diagnostic group, were observed. APOE ε4-associated increases in tau pathology, decreases in glucose uptake, and increases in brain atrophy, which expand in regional scope and magnitude with disease progression, were observed. Significant sex- and age-related differences in APOE ε4-associated neuroimaging biomarker heterogeneity, with overall increases in pathological presentation in female APOE ε4 carriers, were observed. Regional differences in Aβ deposition, tau accumulation, glucose uptake, ventricle size, and white matter hyperintensities were observed in cognitively normal participants who converted to mild cognitive impairment/Alzheimer's disease, which may hold potential predictive value.

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Publication Details

Journal
Alzheimer s & Dementia
Published
2024-11-22
DOI
https://doi.org/10.1002/alz.14392
Citations
6
Primary Topic
Alzheimer's disease research and treatments
Type
article
Field-Weighted Citation Impact
1.96

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article

APOE ε4–associated heterogeneity of neuroimaging biomarkers across the Alzheimer's disease continuum

Jason Mares, Vilas Menon, Anurag Sharma, Laura Beth McIntire et al.
6 citations
Alzheimer s & Dementia
Alzheimer's disease research and treatments
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article

APOE ε4–associated heterogeneity of neuroimaging biomarkers across the Alzheimer's disease continuum

Jason Mares, Vilas Menon, Anurag Sharma, Laura Beth McIntire, Tal Nuriel, Sheina Emrani, Jia Guo, Gautam Kumar
article en
6 citations

Abstract

An extensive study was performed on the apolipoprotein E (APOE) ε4-associated heterogeneity in neuroimaging biomarkers from the Alzheimer's Disease Neuroimaging Initiative. Robust APOE ε4-associated increases in amyloid beta (Aβ) deposition throughout the brain, in every diagnostic group, were observed. APOE ε4-associated increases in tau pathology, decreases in glucose uptake, and increases in brain atrophy, which expand in regional scope and magnitude with disease progression, were observed. Significant sex- and age-related differences in APOE ε4-associated neuroimaging biomarker heterogeneity, with overall increases in pathological presentation in female APOE ε4 carriers, were observed. Regional differences in Aβ deposition, tau accumulation, glucose uptake, ventricle size, and white matter hyperintensities were observed in cognitively normal participants who converted to mild cognitive impairment/Alzheimer's disease, which may hold potential predictive value.

Alzheimer s & DementiaVol. 21(1)
University of Maryland, Baltimore (US), Cornell University (US), Weill Cornell Medicine (US), Columbia University (US), University of Pennsylvania (US)
Foundation for the National Institutes of Health, Alzheimer's Association, Bristol-Myers Squibb, Eli Lilly and Company, Pfizer, Biogen, Meso Scale Diagnostics, BioClinica, Novartis Pharmaceuticals Corporation, Northern California Institute for Research and Education, Eisai, Servier, H. Lundbeck A/S, IXICO, National Institutes of Health, Genentech, Canadian Institutes of Health Research, National Institute on Aging
Good health and well-being
Openalex Percentile: Top 13%
Alzheimer's disease research and treatments
1.96
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