Shoamanesh Ashkan, Martinez-Ramirez Sergi, Oliveira-Filho Jamary, Reijmer Yael, Falcone Guido J, Ayres Alison, Schwab Kristin, Goldstein Joshua N, Rosand Jonathan, Gurol M Edip, Viswanathan Anand, Greenberg Steven M
From the Hemorrhagic Stroke Research Program, Massachusetts General Hospital, Harvard Medical School, Boston, MA.
Neurology. 2014 Nov 11;83(20):1838-43. doi: 10.1212/WNL.0000000000000984. Epub 2014 Oct 15.
We sought to explore the mechanisms leading to cerebral amyloid angiopathy (CAA)-related cortical superficial siderosis (cSS) by examining its neuroimaging and genetic association with cerebral microbleeds (CMBs).
MRI scans of 84 subjects with probable or definite CAA participating in a longitudinal research study were graded for cSS presence and severity (focal, restricted to ≤ 3 sulci vs disseminated, ≥ 4 sulci), and CMB count. APOE ε variants were directly genotyped. We performed cross-sectional analysis comparing CMB counts and APOE ε2 and ε4 allele frequency between subjects with no, focal, or disseminated cSS.
cSS was present in 48% (n = 40) of the population. APOE ε2 was overrepresented among participants with focal (odds ratio [OR] 7.0, 95% confidence interval [CI] 1.7-29.3, p = 0.008) and disseminated (OR 11.5, 95% CI 2.8-46.2, p = 0.001) cSS relative to individuals without cSS. CMB counts decreased with increasing severity of cSS (median: 41, 38, and 15 for no cSS, focal cSS, and disseminated cSS, respectively, p = 0.09). The highest CMB count tertile was associated with APOE ε4 (OR 3.0, 95% CI 1.4-6.6, p = 0.006) relative to the lowest tertile.
Among individuals with advanced CAA, cSS tends to occur in individuals with relatively lower CMB counts and with a distinct pattern of APOE genotypes. These results suggest that CAA-related cSS and CMBs may arise from distinct vasculopathic mechanisms.
我们试图通过研究脑淀粉样血管病(CAA)相关的皮质表面铁沉积(cSS)的神经影像学表现及其与脑微出血(CMB)的基因关联,来探索导致CAA相关cSS的机制。
对84名参与纵向研究的可能或确诊为CAA的受试者进行MRI扫描,对cSS的存在情况和严重程度(局灶性,局限于≤3个脑沟;弥漫性,≥4个脑沟)以及CMB数量进行分级。对APOE ε变异体进行直接基因分型。我们进行了横断面分析,比较了无cSS、局灶性cSS或弥漫性cSS的受试者之间的CMB数量以及APOE ε2和ε4等位基因频率。
48%(n = 40)的人群存在cSS。与无cSS的个体相比,APOE ε2在局灶性(优势比[OR] 7.0,95%置信区间[CI] 1.7 - 29.3,p = 0.008)和弥漫性(OR 11.5,95% CI 2.8 - 46.2,p = 0.001)cSS的参与者中占比过高。CMB数量随着cSS严重程度的增加而减少(无cSS、局灶性cSS和弥漫性cSS的中位数分别为41、38和15,p = 0.09)。相对于最低三分位数,最高CMB数量三分位数与APOE ε4相关(OR 3.0,95% CI 1.4 - 6.6,p = 0.006)。
在晚期CAA患者中,cSS往往发生在CMB数量相对较低且具有独特APOE基因型模式的个体中。这些结果表明,CAA相关的cSS和CMB可能源于不同的血管病变机制。