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Published on: July 28, 2018
Pathological Changes of Small Vessel Disease in Intracerebral Hemorrhage: a Systematic Review and Meta-analysis
Mangmang Xu1,2, Yuyi Zhu1,2, Xindi Song1,2
1Department of Neurology, West China Hospital, Sichuan University, No. 37 Guo Xue Xiang, Chengdu, 610041, Sichuan Province, China.
Insights
Cerebral amyloid angiopathy (CAA) and arteriolosclerosis are linked in intracerebral hemorrhage (ICH). More microbleeds were found in ICH patients with CAA, suggesting a connection between these cerebral small vessel diseases.
Area of Science:
- Neurology
- Pathology
- Radiology
Background:
- Intracerebral hemorrhage (ICH) is often caused by underlying cerebral small vessel diseases (CSVD).
- Cerebral amyloid angiopathy (CAA) and arteriolosclerosis are common CSVD pathologies.
- Understanding the interplay between these pathologies is crucial for diagnosing and managing ICH.
Conclusions:
- Arteriolosclerosis may be associated with severe cerebral amyloid angiopathy in ICH.
- Pathological investigation of CSVD markers in relation to ICH etiology requires further research.
- Direct correlations between MRI and pathology for lacunes, enlarged perivascular spaces, and atrophy are limited.
Abstract:
In intracerebral hemorrhage (ICH) with pathology-proven etiology, we performed a systematic review and meta-analysis to elucidate the association between cerebral amyloid angiopathy (CAA) and arteriolosclerosis, and directly compared MRI and pathological changes of markers of cerebral small vessel disease (CSVD). Studies enrolling primary ICH who had received an etiological diagnosis through biopsy or autopsy were searched using Ovid MEDLINE, PubMed, and Web of Science from inception to June 8, 2022. We extracted pathological changes of CSVD for each patient whenever available. Patients were grouped into CAA + arteriolosclerosis, strict CAA, and strict arteriolosclerosis subgroups. Of 4155 studies identified, 28 studies with 456 ICH patients were included. The frequency of lobar ICH (p<0.001) and total microbleed number (p=0.015) differed among patients with CAA + arteriolosclerosis, strict CAA, and strict arteriolosclerosis. Concerning pathology, severe CAA was associated with arteriolosclerosis (OR 6.067, 95% CI 1.107-33.238, p=0.038), although this association was not statistically significant after adjusting for age and sex. Additionally, the total microbleed number (median 15 vs. 0, p=0.006) was higher in ICH patients with CAA evidence than those without CAA. The pathology of CSVD imaging markers was mostly investigated in CAA-ICH. There was inconsistency concerning CAA severity surrounding microbleeds. Small diffusion-weighted imaging lesions could be matched to acute microinfarct histopathologically. Studies that directly correlated MRI and pathology of lacunes, enlarged perivascular spaces, and atrophy were scarce. Arteriolosclerosis might be associated with severe CAA. The pathological changes of CSVD markers by ICH etiology are needed to be investigated further.
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