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Updated: Jun 18, 2025

Using Retinal Imaging to Study Dementia
Published on: November 6, 2017
Intracranial Atherosclerotic Disease and Incident Dementia: The ARIC Study (Atherosclerosis Risk in Communities)
Di Zhao1, Eliseo Guallar1,2, Ye Qiao3
1Department of Epidemiology, Bloomberg School of Public Health (D.Z., E.G.), Johns Hopkins University, Baltimore, MD.
Insights
Intracranial atherosclerotic disease (ICAD) significantly increases dementia risk, independent of cerebral small vessel disease (CSVD) and other factors. This finding highlights ICAD as a crucial target for dementia prevention strategies.
Area of Science:
- Neuroscience
- Vascular Neurology
- Epidemiology
Background:
- Cerebral small vessel disease (CSVD) is a known contributor to dementia.
- The impact of intracranial atherosclerotic disease (ICAD) on dementia risk in the general population is not well understood.
- This study investigates the association between ICAD and incident dementia.
Purpose of the Study:
- To determine the risk of developing dementia associated with intracranial atherosclerotic disease (ICAD).
- To assess this risk while accounting for cerebral small vessel disease (CSVD) and common cardiovascular risk factors.
- To explore the role of ICAD in dementia development within a US community-based cohort.
Main Methods:
- Utilized brain MRI from 1980 participants in the Atherosclerosis Risk in Communities (ARIC) study.
- Identified ICAD using high-resolution vessel wall MRI and MRA.
- Assessed incident dementia over a median follow-up of 5.6 years using Cox proportional hazard models, adjusting for CSVD markers, APOE4, and cardiovascular risk factors.
Main Results:
- Intracranial atherosclerotic disease (ICAD) was detected in 34.6% of participants.
- ICAD was associated with a 57% increased risk of incident dementia (HR, 1.57; 95% CI, 1.17-2.11) after full adjustment.
- Increased dementia risk was observed even with low-grade ICAD and in individuals with low CSVD burden.
Conclusions:
- Intracranial atherosclerotic disease (ICAD) is an independent risk factor for incident dementia.
- The findings suggest ICAD may mediate the impact of cardiovascular risk factors on cognitive decline.
- Both ICAD and CSVD are critical considerations for understanding vascular contributions to dementia.
Background:
Studies of the neurovascular contribution to dementia have largely focused on cerebral small vessel disease (CSVD), but the role of intracranial atherosclerotic disease (ICAD) remains unknown in the general population. The objective of this study was to determine the risk of incident dementia from ICAD after adjusting for CSVD and cardiovascular risk factors in a US community-based cohort.
Methods:
We acquired brain magnetic resonance imaging examinations from 2011 through 2013 in 1980 Black and White participants in the ARIC study (Atherosclerosis Risk in Communities), a prospective cohort conducted in 4 US communities. Magnetic resonance imaging examinations included high-resolution vessel wall magnetic resonance imaging and magnetic resonance angiography to identify ICAD. Of these participants, 1590 without dementia, without missing covariates, and with adequate magnetic resonance image quality were followed through 2019 for incident dementia. Associations between ICAD and incident dementia were assessed using Cox proportional hazard ratios adjusted for CSVD (characterized by white matter hyperintensities, lacunar infarctions, and microhemorrhages), APOE4 genotype (apolipoprotein E gene ε4), and cardiovascular risk factors.
Results:
The mean age (SD) of study participants was 77.4 (5.2) years. ICAD was detected in 34.6% of participants. After a median follow-up of 5.6 years, 286 participants developed dementia. Compared with participants without ICAD, the fully adjusted hazard ratios (95% CIs) for incident dementia in participants with any ICAD, with ICAD only causing stenosis ≤50%, and with ICAD causing stenosis >50% in ≥1 vessel were 1.57 (1.17-2.11), 1.41 (1.02-1.95), and 1.94 (1.32-2.84), respectively. ICAD was associated with dementia even among participants with low white matter hyperintensities burden, a marker of CSVD.
Conclusions:
ICAD was associated with an increased risk of incident dementia, independent of CSVD, APOE4 genotype, and cardiovascular risk factors. The increased risk of dementia was evident even among participants with low CSVD burden, a group less likely to be affected by vascular dementia, and in participants with ICAD causing only low-grade stenosis. Our results suggest that ICAD may partially mediate the effect that cardiovascular risk factors have on the brain leading to dementia. Both ICAD and CSVD must be considered to understand the vascular contributions to cognitive decline.
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