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Mixed-location cerebral hemorrhage/microbleeds: Underlying microangiopathy and recurrence risk
Marco Pasi1, Andreas Charidimou1, Gregoire Boulouis1
1From the Hemorrhagic Stroke Research Program (M.P., A.C., G.B., E.A., A.A., K.M.S., A.V., S.M.G., M.E.G.), Department of Neurology, Massachusetts General Hospital Stroke Research Center, Harvard Medical School, Boston; NEUROFARBA Department (M.P., L.P.), Neuroscience Section, University of Florence, Italy; Université Paris-Descartes (G.B.), INSERM UMR 894, Department of Neuroradiology, Centre Hospitalier Sainte-Anne, France; and Division of Neurocritical Care and Emergency Neurology (J.N.G., J.R.), Massachusetts General Hospital, Harvard Medical School, Boston.
Objective:
To assess the predominant type of cerebral small vessel disease (SVD) and recurrence risk in patients who present with a combination of lobar and deep intracerebral hemorrhage (ICH)/microbleed locations (mixed ICH).
Methods:
Of 391 consecutive patients with primary ICH enrolled in a prospective registry, 75 (19%) had mixed ICH. Their demographics, clinical/laboratory features, and SVD neuroimaging markers were compared to those of 191 patients with probable cerebral amyloid angiopathy (CAA-ICH) and 125 with hypertensive strictly deep microbleeds and ICH (HTN-ICH). ICH recurrence and case fatality were also analyzed.
Results:
Patients with mixed ICH showed a higher burden of vascular risk factors reflected by a higher rate of left ventricular hypertrophy, higher creatinine values, and more lacunes and severe basal ganglia (BG) enlarged perivascular spaces (EPVS) than patients with CAA-ICH (all p < 0.05). In multivariable models mixed ICH diagnosis was associated with higher creatinine levels (odds ratio [OR] 2.5, 95% confidence interval [CI] 1.2-5.0, p = 0.010), more lacunes (OR 3.4, 95% CI 1.7-6.8), and more severe BG EPVS (OR 5.8, 95% CI 1.7-19.7) than patients with CAA-ICH. Conversely, when patients with mixed ICH were compared to patients with HTN-ICH, they were independently associated with older age (OR 1.03, 95% CI 1.02-1.1), more lacunes (OR 2.4, 95% CI 1.1-5.3), and higher microbleed count (OR 1.6, 95% CI 1.3-2.0). Among 90-day survivors, adjusted case fatality rates were similar for all 3 categories. Annual risk of ICH recurrence was 5.1% for mixed ICH, higher than for HTN-ICH but lower than for CAA-ICH (1.6% and 10.4%, respectively).
Conclusions:
Mixed ICH, commonly seen on MRI obtained during etiologic workup, appears to be driven mostly by vascular risk factors similar to HTN-ICH but demonstrates more severe parenchymal damage and higher ICH recurrence risk.
Insights
Mixed intracerebral hemorrhage (ICH) is linked to vascular risk factors and shows severe brain damage. Patients with mixed ICH face a higher risk of stroke recurrence compared to those with hypertensive ICH.
Area of Science:
- Neurology
- Radiology
- Vascular Medicine
Background:
- Cerebral small vessel disease (SVD) is a common cause of intracerebral hemorrhage (ICH).
- Distinguishing the underlying cause of ICH is crucial for predicting recurrence risk.
Purpose of the Study:
- To evaluate the predominant SVD type and recurrence risk in patients with mixed lobar and deep ICH.
- To compare the characteristics of mixed ICH with cerebral amyloid angiopathy (CAA-ICH) and hypertensive ICH (HTN-ICH).
Main Methods:
- Prospective registry of 391 primary ICH patients.
- Comparison of demographics, clinical features, and neuroimaging markers between mixed ICH (n=75), CAA-ICH (n=191), and HTN-ICH (n=125) groups.
- Analysis of ICH recurrence and case fatality rates.
Main Results:
- Mixed ICH patients exhibited more vascular risk factors, lacunes, and enlarged perivascular spaces compared to CAA-ICH.
- Mixed ICH was independently associated with older age, more lacunes, and higher microbleed counts versus HTN-ICH.
- Annual ICH recurrence risk was 5.1% for mixed ICH, lower than CAA-ICH (10.4%) but higher than HTN-ICH (1.6%).
Conclusions:
- Mixed ICH is often associated with vascular risk factors, similar to HTN-ICH.
- Mixed ICH demonstrates more severe parenchymal damage and a higher risk of recurrence than HTN-ICH.
- Understanding mixed ICH is vital for accurate diagnosis and management of SVD.
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