Abstract

BackgroundThe key imaging features of cerebral amyloid angiopathy (CAA) are lobar, cortical, or cortico-subcortical microbleeds, macrohaemorrhages and cortical superficial siderosis (cSS). In contrast, hypertensive angiopathy is characterized by (micro) haemorrhages in the basal ganglia, thalami, periventricular white matter or the brain stem. Another distinct form of haemorrhagic microangiopathy is mixed cerebral microbleeds (mixed CMB) with features of both CAA and hypertensive angiopathy. The distinction between the two entities (CAA and mixed CMB) is clinically relevant because the risk of haemorrhage and stroke should be well balanced if oral anticoagulation is indicated in CAA patients. We aimed to comprehensively compare these two entities.MethodsPatients with probable CAA according to the modified Boston criteria and mixed CMB without macrohaemorrhage were retrospectively identified from our database. Comprehensive comparison regarding clinical and radiological parameters was performed between the two cohorts.ResultsPatients with CAA were older (78 ± 8 vs. 74 ± 9 years, p = 0.036) and had a higher prevalence of cSS (19% vs. 4%, p = 0.027) but a lower prevalence of lacunes (73% vs. 50%, p = 0.018) and deep lacunes (23% vs. 51%, p = 0.0003) compared to patients with mixed CMB. Logistic regression revealed an association between the presence of deep lacunes and mixed CMB. The other collected parameters did not reveal a significant difference between the two groups.ConclusionsCAA and mixed CMB demonstrate radiological differences in the absence of macrohaemorrhages. However, more clinically available biomarkers are needed to elucidate the contribution of CAA and hypertensive angiopathy in mixed CMB patients.

Highlights

  • The key pathological feature of cerebral amyloid angiopathy (CAA) is amyloid deposition in small cerebral parenchymal and leptomeningeal vessels [1]

  • Mixed CMB is characterized by additional deephaemorrhages in the basal ganglia, thalami, periventricular white matter or the brain stem whose presence preclude the diagnosis of CAA [4]

  • Patients screened for cerebral metastasis had no signs of intracranial malignant manifestation neither in the MRI of interest nor in follow-up imaging. 22 out of 33 and 18 out of 24 patients with suspected stroke were diagnosed with an acute ischemic stroke in the CAA and mixed CMB group respectively

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Summary

Introduction

The key pathological feature of cerebral amyloid angiopathy (CAA) is amyloid deposition in small cerebral parenchymal and leptomeningeal vessels [1]. Mixed CMB is characterized by additional deep (micro)haemorrhages in the basal ganglia, thalami, periventricular white matter or the brain stem whose presence preclude the diagnosis of CAA [4]. It is unclear whether mixed CMB is a mixed form of CAA with the additional feature of hypertensive haemorrhages. Hypertensive angiopathy is characterized by (micro) haemorrhages in the basal ganglia, thalami, periventricular white matter or the brain stem Another distinct form of haemorrhagic microangiopathy is mixed cerebral microbleeds (mixed CMB) with features of both CAA and hypertensive angiopathy. More clinically available biomarkers are needed to elucidate the contribution of CAA and hypertensive angiopathy in mixed CMB patients

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