Brain perivascular space imaging across the human lifespan

被引:16
|
作者
Lynch, Kirsten M. [1 ,3 ]
Sepehrband, Farshid [1 ,2 ]
Toga, Arthur W. [1 ]
Choupan, Jeiran [1 ,2 ]
机构
[1] USC Keck Sch Med, USC Mark & Mary Stevens Inst Neuroimaging & Inform, Lab Neuro Imaging LONI, Los Angeles, CA 90033 USA
[2] NeuroScope Inc, New York, NY USA
[3] Univ Southern Calif, USC Stevens Neuroimaging & Informat Inst, Keck Sch Med USC, 2025 Zonal Ave, Los Angeles, CA 90033 USA
基金
美国国家卫生研究院;
关键词
Perivascular spaces; Waste clearance; Lifespan; Aging; Morphology; Neuroimaging; Cerebrovascular; VIRCHOW-ROBIN SPACES; CYTOKINE-INDUCED CYCLOOXYGENASE-2; SMALL VESSEL DISEASE; BLOOD-PRESSURE; MRI; ESTROGEN; PATHWAYS; ARTERY; ATHEROSCLEROSIS; SEGMENTATION;
D O I
10.1016/j.neuroimage.2023.120009
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Enlarged perivascular spaces (PVS) are considered a biomarker for vascular pathology and are observed in normal aging and neurological conditions; however, research on the role of PVS in health and disease are hindered by the lack of knowledge regarding the normative time course of PVS alterations with age. To this end, we characterized the influence of age, sex and cognitive performance on PVS anatomical characteristics in a large cross-sectional cohort ( similar to 1400) of healthy subjects between 8 and 90 years of age using multimodal structural MRI data. Our results show age is associated with wider and more numerous MRI-visible PVS over the course of the lifetime with spatially-varying patterns of PVS enlargement trajectories. In particular, regions with low PVS volume fraction in childhood are associated with rapid age-related PVS enlargement (e.g., temporal regions), while regions with high PVS volume fraction in childhood are associated with minimal age-related PVS alterations (e.g., limbic regions). PVS burden was significantly elevated in males compared to females with differing morphological time courses with age. Together, these findings contribute to our understanding of perivascular physiology across the healthy lifespan and provide a normative reference for the spatial distribution of PVS enlargement patterns to which pathological alterations can be compared.
引用
收藏
页数:15
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