From the Hemorrhagic Stroke Research Program, J. Philip Kistler Stroke Research Center, Department of Neurology (T.P., P.F., M.P., G.B., L.X., A.D.W., K.M.S., J.R., M.E.G., S.M.G., A.V., A.C.), and Division of Neurocritical Care and Emergency Neurology (J.R.), Massachusetts General Hospital, and MIND Informatics, Massachusetts General Hospital Biomedical Informatics Core (J.R.), Harvard Medical School, Boston; and Department of Pharmacology, Faculty of Medicine (T.P.), Chulalongkorn University, Bangkok, Thailand.
Neurology. 2020 Apr 28;94(17):e1853-e1865. doi: 10.1212/WNL.0000000000009321. Epub 2020 Apr 13.
To investigate the prevalence, predictors, and clinical relevance of cortical superficial siderosis (cSS) progression in cerebral amyloid angiopathy (CAA).
Consecutive patients with symptomatic CAA meeting Boston criteria in a prospective cohort underwent baseline and follow-up MRI within 1 year. cSS progression was evaluated on an ordinal scale and categorized into mild (score 1-2 = cSS extension within an already present cSS focus or appearance of 1 new cSS focus) and severe progression (score 3-4 = appearance of ≥2 new cSS foci). Binominal and ordinal multivariable logistic regression were used to determine cSS progression predictors. We investigated future lobar intracerebral hemorrhage (ICH) risk in survival analysis models.
We included 79 patients with CAA (mean age, 69.2 years), 56 (71%) with lobar ICH at baseline. cSS progression was detected in 23 (29%) patients: 15 (19%) patients had mild and 8 (10%) severe progression. In binominal multivariable logistic regression, ICH presence (odds ratio [OR], 7.54; 95% confidence interval [CI], 1.75-53.52; = 0.016) and baseline cSS (OR, 10.41; 95% CI, 2.84-52.83; = 0.001) were independent predictors of cSS progression. In similar models, presence of disseminated (but not focal) cSS at baseline (OR, 5.58; 95% CI, 1.81-19.41; = 0.004) was an independent predictor of cSS progression. Results were similar in ordinal multivariable logistic regression models. In multivariable Cox regression analysis, severe cSS progression was independently associated with increased future ICH risk (HR, 5.90; 95% CI, 1.30-26.68; = 0.021).
cSS evolution on MRI is common in patients with symptomatic CAA and might be a potential biomarker for assessing disease severity and future ICH risk. External validation of these findings is warranted.
研究脑淀粉样血管病(CAA)中皮质表面铁沉积(cSS)进展的患病率、预测因素和临床相关性。
在一项前瞻性队列研究中,连续纳入符合波士顿标准的有症状 CAA 患者,在 1 年内进行基线和随访 MRI 检查。采用有序量表评估 cSS 进展情况,并分为轻度(评分 1-2=已有 cSS 灶内扩展或出现 1 个新 cSS 灶)和重度进展(评分 3-4=出现≥2 个新 cSS 灶)。采用二项式和有序多变量逻辑回归来确定 cSS 进展的预测因素。我们在生存分析模型中研究了未来的皮质下脑叶内出血(ICH)风险。
我们纳入了 79 例 CAA 患者(平均年龄 69.2 岁),其中 56 例(71%)患者在基线时存在脑叶 ICH。23 例(29%)患者出现 cSS 进展:15 例(19%)患者为轻度进展,8 例(10%)患者为重度进展。在二项式多变量逻辑回归中,ICH 存在(比值比[OR],7.54;95%置信区间[CI],1.75-53.52;P=0.016)和基线 cSS(OR,10.41;95%CI,2.84-52.83;P=0.001)是 cSS 进展的独立预测因素。在类似的模型中,基线时存在弥散性(而非局灶性)cSS(OR,5.58;95%CI,1.81-19.41;P=0.004)是 cSS 进展的独立预测因素。在有序多变量逻辑回归模型中,结果相似。在多变量 Cox 回归分析中,严重的 cSS 进展与未来 ICH 风险增加独立相关(HR,5.90;95%CI,1.30-26.68;P=0.021)。
有症状 CAA 患者的 MRI 上 cSS 演变很常见,可能是评估疾病严重程度和未来 ICH 风险的潜在生物标志物。需要进行这些发现的外部验证。