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Updated: Sep 7, 2025

Using Retinal Imaging to Study Dementia
Published on: November 6, 2017
Associations of Vascular Risk and Amyloid Burden with Subsequent Dementia
Rebecca F Gottesman1, Aozhou Wu2, Josef Coresh2
1National Institute of Neurological Disorders and Stroke Intramural Program, National Institutes of Health, Bethesda, MD, USA.
Objective:
Midlife vascular risk factors (MVRFs) are associated with incident dementia, as are amyloid β (Aβ) deposition and neurodegeneration. Whether vascular and Alzheimer disease-associated factors contribute to dementia independently or interact synergistically to reduce cognition is poorly understood.
Methods:
Participants in the Atherosclerosis Risk in Communities-Positron Emission Tomography study were followed from 1987-1989 (45-64 years old) through 2016-2017 (74-94 years old), with repeat cognitive assessment and dementia adjudication. In 2011-2013, dementia-free participants underwent brain magnetic resonance imaging (with white matter hyperintensity [WMH] and brain volume measurement) and florbetapir (Aβ) positron emission tomography. The relative contributions of vascular risk and injury (MVRFs, WMH volume), elevated Aβ standardized uptake value ratio (SUVR), and neurodegeneration (smaller temporoparietal brain regions) to incident dementia were evaluated with adjusted Cox models.
Results:
In 298 individuals, 36 developed dementia (median follow-up = 4.9 years). Midlife hypertension and Aβ each independently predicted dementia risk (hypertension: hazard ratio [HR] = 2.57, 95% confidence interval [CI] = 1.16-5.67; Aβ SUVR [per standard deviation (SD)]: HR = 2.57, 95% CI = 1.72-3.84), but did not interact significantly, whereas late life diabetes (HR = 2.50, 95% CI = 1.18-5.28) and Aβ independently predicted dementia risk. WMHs (per SD: HR = 1.51, 95% CI = 1.03-2.20) and Aβ SUVR (HR = 2.52, 95% CI = 1.83-3.47) independently contributed to incident dementia, but WMHs lost significance when MVRFs were included. Smaller temporoparietal brain regions were associated with incident dementia, independent of Aβ and MVRFs (HR = 2.18, 95% CI = 1.18-4.01).
Interpretation:
Midlife hypertension and late life Aβ are independently associated with dementia risk, without evidence for synergy on a multiplicative scale. Given the independent contributions of vascular and amyloid mechanisms, multiple pathways should be considered when evaluating interventions to reduce the burden of dementia. ANN NEUROL 2022;92:607-619.
Insights
Midlife hypertension and amyloid-beta (Aβ) independently increase dementia risk. These factors, along with neurodegeneration, contribute to cognitive decline through separate pathways, not synergistic effects.
Area of Science:
- Neurology
- Neuroscience
- Public Health
Background:
- Midlife vascular risk factors (MVRFs) and Alzheimer's disease (AD) pathologies like amyloid-beta (Aβ) deposition are linked to dementia.
- The independent or synergistic contributions of vascular and AD-related factors to cognitive decline remain unclear.
Purpose of the Study:
- To investigate the independent and interactive effects of MVRFs, Aβ deposition, and neurodegeneration on incident dementia risk.
Main Methods:
- Longitudinal Atherosclerosis Risk in Communities-Positron Emission Tomography (ARIC-PET) study data were analyzed.
- Participants (45-64 years) were followed for cognitive changes, with brain MRI and Aβ PET imaging conducted in late life.
- Cox models assessed the contributions of MVRFs, white matter hyperintensities (WMHs), Aβ, and neurodegeneration to dementia risk.
Main Results:
- Midlife hypertension and late-life Aβ independently predicted dementia risk.
- White matter hyperintensities (WMHs) and smaller brain volumes were also associated with increased dementia risk.
- No significant multiplicative interaction was found between vascular factors and Aβ for dementia risk.
Conclusions:
- Midlife hypertension and late-life Aβ independently contribute to dementia risk.
- Intervention strategies for dementia prevention should consider the distinct roles of vascular and amyloid pathways.
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