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Published on: March 7, 2019
Differences in lobar microbleed topography in cerebral amyloid angiopathy and hypertensive arteriopathy
Pin-Yan Kuo1, Hsin-Hsi Tsai2, Bo-Ching Lee3
1Department of Medical Education, National Taiwan University Hospital, Taipei, Taiwan.
Insights
Cerebral amyloid angiopathy (CAA) is strongly linked to intracortical lobar microbleeds, while hypertensive arteriolosclerosis is associated with subcortical ones. Anatomical location of microbleeds helps differentiate these conditions.
Area of Science:
- Neurology
- Neuroimaging
- Cerebrovascular Diseases
Background:
- Lobar cerebral microbleeds are observed in both cerebral amyloid angiopathy (CAA) and hypertensive arteriolosclerosis.
- Distinguishing between these conditions based on microbleed location is crucial for accurate diagnosis.
Purpose of the Study:
- To investigate the association between the anatomical location of lobar microbleeds and the underlying microangiopathy (CAA vs. hypertensive arteriolosclerosis).
- To determine if microbleed categorization can improve neuroimaging accuracy for cerebral small vessel disease.
Main Methods:
- Ninety-one intracerebral hemorrhage survivors with lobar microbleeds underwent brain MRI and amyloid PET.
- Lobar microbleeds were categorized as intracortical, juxtacortical, or subcortical.
- Associations between microbleed location, microangiopathy subtypes, and amyloid deposition (Pittsburgh Compound-B PET SUVR) were assessed.
Main Results:
- Patients with CAA showed a higher prevalence of intracortical lobar microbleeds (80.0%) and lower prevalence of subcortical ones (13.3%) compared to hypertensive arteriolosclerosis patients.
- Strictly intracortical/juxtacortical microbleeds were associated with CAA (OR 18.9), while subcortical microbleeds were linked to hypertensive arteriolosclerosis (OR 10.9).
- Higher amyloid retention correlated with intracortical microbleeds and inversely with subcortical microbleeds.
Conclusions:
- Strictly intracortical/juxtacortical lobar microbleeds are more strongly associated with CAA and cortical amyloid deposition than subcortical microbleeds.
- Categorizing lobar microbleeds by location aids in differentiating underlying microangiopathies.
- This approach may enhance the accuracy of neuroimaging for cerebral small vessel disease diagnosis.
Abstract:
Lobar cerebral microbleeds are a characteristic neuroimaging finding in cerebral amyloid angiopathy (CAA) but can also be found in hypertensive arteriolosclerosis. We aimed to investigate whether CAA is more associated with intracortical lobar microbleeds than hypertensive arteriosclerosis. Ninety-one survivors of spontaneous intracerebral hemorrhage with at least one lobar microbleed were included and underwent brain MRI and amyloid PET. We categorized lobar microbleeds as intracortical, juxtacortical, or subcortical. We assessed the associations between the lobar microbleed categories and microangiopathy subtypes or cerebral amyloid load based on the Pittsburgh Compound-B PET standardized uptake value ratio (SUVR). Patients with CAA had a higher prevalence of intracortical lobar microbleeds (80.0% vs. 50.8%, P = 0.011) and lower prevalence of subcortical lobar microbleeds (13.3% vs. 60.1%, P < 0.001) than patients with hypertensive arteriolosclerosis. Strictly intracortical/juxtacortical lobar microbleeds were associated with CAA (OR 18.9 [1.9-191.4], P = 0.013), while the presence of subcortical lobar microbleeds was associated with hypertensive arteriolosclerosis (OR 10.9 [1.8-68.1], P = 0.010). Amyloid retention was higher in patients with strictly intracortical/juxtacortical CMBs than those without (SUVR = 1.15 [1.05-1.52] vs. 1.08 [1.02-1.19], P = 0.039). Amyloid retention positively correlated with the number of intracortical lobar microbleeds (P < 0.001) and negatively correlated with the number of subcortical lobar microbleeds (P = 0.018). CAA and cortical amyloid deposition are more strongly associated with strictly intracortical/juxtacortical microbleeds than subcortical lobar microbleeds. Categorization of lobar microbleeds based on anatomical location may help differentiate the underlying microangiopathy and potentially improve the accuracy of current neuroimaging criteria for cerebral small vessel disease.
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