Cerebral Amyloid Angiopathy and Cerebral Amyloid Angiopathy-Related Inflammation: Comparison of Hemorrhagic and DWI MRI Features

被引:21
|
作者
Renard, Dimitri [1 ]
Tatu, Lavinia [1 ]
Collombier, Laurent [2 ]
Wacongne, Anne [1 ]
Ayrignac, Xavier [3 ]
Charif, Mahmoud [3 ]
Boukriche, Yassine [4 ]
Chiper, Laura [4 ]
Fourcade, Genevieve [5 ]
Azakri, Souhayla [3 ]
Gaillard, Nicolas [6 ]
Mercier, Erick [7 ]
Lehmann, Sylvain [8 ]
Thouvenot, Eric [1 ,9 ]
机构
[1] Nimes Univ Hosp, Dept Neurol, Nimes, France
[2] Nimes Univ Hosp, Dept Nucl Med, Nimes, France
[3] Montpellier Univ Hosp, Dept Neurol, Montpellier, France
[4] CH Beziers, Dept Neurol, Beziers, France
[5] CH Narbonne, Dept Neurol, Narbonne, France
[6] CH Perpignan, Dept Neurol, Perpignan, France
[7] Nimes Univ Hosp, Dept Hematol, Nimes, France
[8] Univ Montpellier, Hop St Eloi, CHU Montpellier, Lab Biochim Prote Clin IRMB CRB Inserm U11183, Montpellier, France
[9] Univ Montpellier, UMR5203, Inst Genom Fonct, Montpellier, France
关键词
Amyloid imaging; apolipoprotein E genotype; cerebral amyloid angiopathy; cerebral amyloid angiopathy-related inflammation; cerebral microbleeds; cerebrospinal fluid; florbetaben; intracerebral hemorrhage; positron emission tomography; BETA-RELATED ANGIITIS; CORTICAL SUPERFICIAL SIDEROSIS; CENTRAL-NERVOUS-SYSTEM; SUBARACHNOID HEMORRHAGE; CEREBROSPINAL-FLUID; BOSTON CRITERIA; DIAGNOSIS; PET; MICROBLEEDS; VALIDATION;
D O I
10.3233/JAD-180269
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Cerebral amyloid angiopathy (CAA) can be associated with primary vasculitis of small/medium-sized leptomeningeal and cortical arteries, called CAA-related inflammation (CAA-ri). Objective: To compare hemorrhagic and diffusion-weighted imaging (DWI) MRI features in CAA and CAA-ri. Methods: We prospectively scored in a consecutive CAA and CAA-ri cohort: presence/number of chronic intracerebral hemorrhage (ICH), cerebral microbleeds (CMB), and cortical superficial siderosis (CSS) on initial T2*-weighted imaging, and DWI lesions on both initial and follow-up imaging. In a subgroup, ApoE, CSF, and 18F-florbetaben-positron emission tomography (FBB-PET) were also analyzed. Results: In CAA-ri, CMB presence was more frequent (100% versus 40%, p < 0.001) and CMB numbers higher (mean 137 versus 8, p < 0.001). No difference was observed for chronic ICH or CSS. DWI lesions were more frequent in acute compared to chronic CAA-ri (p = 0.025), whereas no such difference was observed between acute and chronic CAA (p = 0.18). Both ApoE4 (genotyping available in 22 CAA-ri and 48 CAA patients) carriers and homozygosity were more frequent in CAA-ri (48% versus 19% [p = 0.014] and 32% versus 2% [p < 0.001] respectively). CSF biomarker analyses (performed in 20 CAA-ri and 45 CAA patients) showed lower A1342 levels in CAA-ri compared to CAA (median 312 versus 422 pg/mL, p = 0.0032). FBB-PET (performed in 11 CAA-ri and 20 CAA patients) showed higher standardized uptake value ratios in CAA-ri compared with CAA, only significant when the pons was used as reference (p = 0.037). Conclusion: Compared to CAA, CAA-ri was associated with higher CMB numbers, more frequent ApoE4 carriers and homozygotes, lower CSF A1342 levels, and more severe amyloid load on FBB-PET.
引用
收藏
页码:1113 / 1121
页数:9
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