Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Alzheimer's Disease Research Unit, McGill Centre for Studies in Aging, Montreal, Canada.
Ann Neurol. 2023 Sep;94(3):442-456. doi: 10.1002/ana.26710. Epub 2023 Jun 14.
OBJECTIVES: Glymphatic function has not yet been explored in behavioral variant frontotemporal dementia (bvFTD). The spatial correlation between regional glymphatic function and bvFTD remains unknown. METHOD: A total of 74 patients with bvFTD and 67 age- and sex-matched healthy controls (HCs) were selected from discovery dataset and replication dataset. All participants underwent neuropsychological assessment. Glymphatic measures including choroid plexus (CP) volume, diffusion tensor imaging along the perivascular (DTI-ALPS) index, and coupling between blood-oxygen-level-dependent signals and cerebrospinal fluid signals (BOLD-CSF coupling), were compared between the two groups. Regional glymphatic function was evaluated by dividing DTI-ALPS and BOLD-CSF coupling into anterior, middle, and posterior regions. The bvFTD-related metabolic pattern was identified using spatial covariance analysis based on F-FDG-PET. RESULTS: Patients with bvFTD showed higher CP volume (p < 0.001); anterior and middle DTI-ALPS (p < 0.001); and weaker anterior BOLD-CSF coupling (p < 0.05) than HCs after controlling for cortical gray matter volume in both datasets. In bvFTD from the discovery dataset, the anterior DTI-ALPS was negatively associated with the expression of the bvFTD-related metabolic pattern (r = -0.52, p = 0.034) and positively related with regional standardized uptake value ratios of F-FDG-PET in bvFTD-related brain regions (r range: 0.49 to 0.62, p range: 0.017 to 0.047). Anterior and middle glymphatic functions were related to global cognition and disease severity. INTERPRETATION: Our findings reveal abnormal glymphatic function, especially in the anterior and middle regions of brain in bvFTD. Regional glymphatic dysfunction may contribute to the pathogenesis of bvFTD. ANN NEUROL 2023;94:442-456.
目的:糖质新生功能在行为变异型额颞叶痴呆(bvFTD)中尚未得到探索。区域糖质新生功能与 bvFTD 之间的空间相关性尚不清楚。
方法:从发现数据集和复制数据集中共选择了 74 名 bvFTD 患者和 67 名年龄和性别匹配的健康对照者(HCs)。所有参与者均接受神经心理学评估。比较两组之间脉络丛(CP)体积、血管周围弥散张量成像(DTI-ALPS)指数、血氧水平依赖性信号与脑脊液信号之间的耦合(BOLD-CSF 耦合)等糖质新生指标。通过将 DTI-ALPS 和 BOLD-CSF 耦合分为前、中、后三个区域来评估区域糖质新生功能。基于 18F-FDG-PET 的空间协方差分析确定与 bvFTD 相关的代谢模式。
结果:与 HCs 相比,bvFTD 患者 CP 体积较高(p<0.001),前、中 DTI-ALPS 较高(p<0.001),前 BOLD-CSF 耦合较弱(p<0.05),而在两个数据集均控制皮质灰质体积后。在发现数据集中的 bvFTD 中,前 DTI-ALPS 与 bvFTD 相关代谢模式的表达呈负相关(r=-0.52,p=0.034),与 bvFTD 相关脑区 18F-FDG-PET 的区域标准化摄取比值呈正相关(r 范围:0.49 至 0.62,p 范围:0.017 至 0.047)。前、中糖质新生功能与整体认知和疾病严重程度相关。
结论:我们的发现揭示了 bvFTD 中异常的糖质新生功能,尤其是在前、中脑区。区域糖质新生功能障碍可能有助于 bvFTD 的发病机制。ANN NEUROL 2023;94:442-456。
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