Hsin-Hsi Tsai, Chia-Ju Liu, Bo-Ching Lee, Ya-Fang Chen, R. Yen, J. Jeng, Li-Kai Tsai
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Multivariable regression models were employed to assess radio-clinical features related to cerebral tau pathology in cerebral amyloid angiopathy.\n Cerebral amyloid angiopathy exhibited a higher cerebral tau burden in the inferior temporal lobe (1.25 [1.17‒1.42] vs. 1.08 [1.05‒1.22], P<0.001) and all Braak stage regions of interest (P<0.05) than hypertensive small vessel disease, though the differences were attenuated after age adjustment. Cerebral tau pathology was significantly associated with cerebral amyloid angiopathy-related vascular markers, including cortical superficial siderosis (β=0.12, 95% confidence interval 0.04‒0.21) and cerebral amyloid angiopathy score (β=0.12, 95% confidence interval 0.03‒0.21) after adjustment for age, ApoE4 status and whole cortex amyloid load. Tau pathology correlated significantly with cognitive score (Spearman’s ρ=-0.56, P=0.001) and hippocampal volume (-0.49, P=0.007), even after adjustment.\n In conclusion, tau pathology is more frequent in sporadic cerebral amyloid angiopathy than hypertensive small vessel disease. Cerebral amyloid angiopathy-related vascular pathologies, especially cortical superficial siderosis, are potential markers of cerebral tau pathology suggestive of concomitant Alzheimer’s disease.","PeriodicalId":9318,"journal":{"name":"Brain Communications","volume":"45 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-03-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Cerebral tau pathology in cerebral amyloid angiopathy\",\"authors\":\"Hsin-Hsi Tsai, Chia-Ju Liu, Bo-Ching Lee, Ya-Fang Chen, R. Yen, J. 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引用次数: 0
摘要
Tau是阿尔茨海默病的特征之一,但在脑淀粉样血管病中的特征并不明显。我们旨在评估 tau PET 扫描与脑淀粉样血管病之间的临床放射学相关性。我们使用 11C- 匹兹堡化合物 B 和 18F-T807 PET 评估了可能患有脑淀粉样血管病(31 人)和高血压小血管病(27 人)的患者的脑淀粉样蛋白和高磷酸化 tau。采用多变量回归模型评估与脑淀粉样血管病中脑tau病理相关的放射临床特征。与高血压性小血管病相比,脑淀粉样血管病在颞下叶(1.25 [1.17-1.42] vs. 1.08 [1.05-1.22],P<0.001)和所有布拉克分期相关区域(P<0.05)表现出更高的脑tau负荷,但经年龄调整后差异减小。在对年龄、载脂蛋白E4状态和整个皮层淀粉样蛋白负荷进行调整后,脑tau病理学与脑淀粉样血管病变相关的血管标记物显著相关,包括皮层浅层苷脂沉积(β=0.12,95%置信区间为0.04-0.21)和脑淀粉样血管病变评分(β=0.12,95%置信区间为0.03-0.21)。即使经过调整,Tau病理与认知评分(Spearman's ρ=-0.56,P=0.001)和海马体积(-0.49,P=0.007)也有显著相关性。总之,在散发性脑淀粉样血管病中,tau病理学比高血压小血管病更常见。与脑淀粉样血管病变相关的血管病变,尤其是皮质表层菱形细胞增多症,是脑tau病变的潜在标志物,提示可能并发阿尔茨海默病。
Cerebral tau pathology in cerebral amyloid angiopathy
Tau, a hallmark of Alzheimer’s disease, is poorly characterized in cerebral amyloid angiopathy. We aimed to assess the clinico-radiological correlations between tau PET scans and cerebral amyloid angiopathy.
We assessed cerebral amyloid and hyperphosphorylated tau in patients with probable cerebral amyloid angiopathy (n=31) and hypertensive small vessel disease (n=27) using 11C- Pittsburgh compound B and 18F-T807 PET. Multivariable regression models were employed to assess radio-clinical features related to cerebral tau pathology in cerebral amyloid angiopathy.
Cerebral amyloid angiopathy exhibited a higher cerebral tau burden in the inferior temporal lobe (1.25 [1.17‒1.42] vs. 1.08 [1.05‒1.22], P<0.001) and all Braak stage regions of interest (P<0.05) than hypertensive small vessel disease, though the differences were attenuated after age adjustment. Cerebral tau pathology was significantly associated with cerebral amyloid angiopathy-related vascular markers, including cortical superficial siderosis (β=0.12, 95% confidence interval 0.04‒0.21) and cerebral amyloid angiopathy score (β=0.12, 95% confidence interval 0.03‒0.21) after adjustment for age, ApoE4 status and whole cortex amyloid load. Tau pathology correlated significantly with cognitive score (Spearman’s ρ=-0.56, P=0.001) and hippocampal volume (-0.49, P=0.007), even after adjustment.
In conclusion, tau pathology is more frequent in sporadic cerebral amyloid angiopathy than hypertensive small vessel disease. Cerebral amyloid angiopathy-related vascular pathologies, especially cortical superficial siderosis, are potential markers of cerebral tau pathology suggestive of concomitant Alzheimer’s disease.