Microbleed topography, leukoaraiosis, and cognition in probable Alzheimer disease from the Sunnybrook dementia study
Jacqueline A Pettersen1, Gayathri Sathiyamoorthy, Fu-Qiang Gao
1Division of Neurology, Department of Medicine, Sunnybrook Health Sciences Centre, A421-2075 Bayview Ave, Toronto, ON M4N 3M5, Canada. jacqui.pettersen@utoronto.ca
Background:
Microbleeds are hemosiderin deposits around small vessels and are well visualized with T2*-weighted gradient-recalled echo (GRE) imaging.
Objectives:
To determine frequency and topography of microbleeds in Alzheimer disease (AD) and to assess their association with leukoaraiosis and cognition.
Design:
Case-control cross-sectional analysis. Microbleeds were counted using GRE imaging. Leukoaraiosis was rated on T2-weighted and proton density-weighted scans using the Age-Related White Matter Changes Rating Scale (ARWMC). Neuropsychological tests indexed cognition.
Setting:
The Cognitive Neurology Clinic, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.
Patients:
Individuals with probable AD (n = 80) and healthy controls (n = 25) from a longitudinal cohort with GRE sequences as part of standard imaging protocol (2002-2006).
Results:
Microbleeds occurred in 29% of patients with AD and 12% of controls and were multiple (> 1) in 48% of patients with AD and 33% of controls. There was lobar (vs centrencephalic) predominance in 92% of AD patients, with occipital lobes accounting for 57% of these microbleeds. The ARWMC scores (P < .005) were significantly higher in AD patients with microbleeds than in those without, and microbleeds correlated with total (r = 0.39, P = .01) and parietooccipital (r = 0.28, P < .01) ARWMC scores. We were unable to demonstrate an association between microbleeds (or leukoaraiosis) and cognitive performance.
Conclusions:
Occipital predominance of microbleeds with corresponding parietooccipital leukoaraiosis has not been well described in prior imaging studies of AD. Microbleeds were frequent, often multiple, and predicted greater leukoaraiosis. These findings illustrate the complexity of AD vasculopathy and the need for additional studies in dementia and stroke populations.
Insights
Microbleeds, often multiple, are frequent in Alzheimer disease (AD) patients and show a distinct occipital lobe pattern. These findings highlight the complex vasculopathy in AD.
Area of Science:
- Neuroimaging
- Neurology
- Vascular Dementia
Background:
- Microbleeds, visualized by T2*-weighted gradient-recalled echo (GRE) imaging, represent hemosiderin deposits around small cerebral vessels.
- Alzheimer disease (AD) is a progressive neurodegenerative disorder with complex underlying pathologies.
Purpose of the Study:
- To determine the frequency and topographical distribution of microbleeds in individuals with probable AD.
- To assess the association between microbleeds, leukoaraiosis, and cognitive function in AD.
Main Methods:
- A case-control, cross-sectional analysis was performed using GRE imaging to count microbleeds.
- Leukoaraiosis was evaluated using the Age-Related White Matter Changes Rating Scale (ARWMC) on T2-weighted and proton density-weighted scans.
- Cognitive performance was assessed using standardized neuropsychological tests.
Main Results:
- Microbleeds were observed in 29% of AD patients versus 12% of controls, frequently occurring as multiple lesions (48% in AD).
- A significant lobar predominance of microbleeds was noted in AD patients (92%), particularly in the occipital lobes (57%).
- AD patients with microbleeds exhibited higher ARWMC scores, with correlations found between microbleeds and total/parietooccipital ARWMC scores.
Conclusions:
- The study identified an occipital predominance of microbleeds and associated parietooccipital leukoaraiosis in AD, a pattern not extensively documented previously.
- Microbleeds were frequent, often multiple, and correlated with increased leukoaraiosis, suggesting a role in AD vasculopathy.
- Further research in dementia and stroke populations is warranted to elucidate the implications of these vascular findings in AD.
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