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Regional changes in cerebral perfusion with age when accounting for changes in gray-matter volume
被引:0
|作者:
Hu, Jian
[1
,2
]
Craig, Martin S.
[1
,2
]
Knight, Silvin P.
[3
,4
]
De Looze, Celine
[3
,4
]
Meaney, James F.
[4
,5
]
Kenny, Rose Anne
[3
,4
,6
,7
]
Chen, Xin
[8
]
Chappell, Michael A.
[1
,2
]
机构:
[1] Univ Nottingham, Mental Hlth & Clin Neurosci, Sch Med, Nottingham, England
[2] Univ Nottingham, Sir Peter Mansfield Imaging Ctr, Sch Med, Nottingham, England
[3] Trinity Coll Dublin, Irish Longitudinal Study Ageing, Sch Med, Dublin, Ireland
[4] Trinity Coll Dublin, Sch Med, Dublin, Ireland
[5] St James Hosp, Natl Ctr Adv Med Imaging, Dublin, Ireland
[6] Trinity Coll Dublin, Global Brain Hlth Inst, Dublin, Ireland
[7] St James Hosp, Mercers Inst Successful Ageing, Dublin, Ireland
[8] Univ Nottingham, Sch Comp Sci, Intelligent Modelling & Anal Grp, Nottingham, England
基金:
英国工程与自然科学研究理事会;
关键词:
arterial spin labeling;
brain atrophy;
partial volume effects correction;
perfusion;
surface-based analysis;
SURFACE-BASED ANALYSIS;
BLOOD-FLOW;
ARTERIAL;
BRAIN;
CORTEX;
MRI;
PET;
HEMODYNAMICS;
OPTIMIZATION;
DEPENDENCE;
D O I:
暂无
中图分类号:
R8 [特种医学];
R445 [影像诊断学];
学科分类号:
1002 ;
100207 ;
1009 ;
摘要:
Purpose: One possible contributing factor for cerebral blood flow (CBF) decline in normal aging is the increase in partial volume effects due to brain atrophy, as cortical thinning can exacerbate the contamination of gray-matter (GM) voxels by other tissue types. This work investigates CBF changes in normal aging of a large elderly cohort aged 54 to 84 and how correction for partial volume effects that would accommodate potential changes in GM might affect this. Methods: The study cohort consisted of 474 participants aged 54 to 84years using pseudo-continuous arterial spin labeling MRI. A volumetric pipeline and a surface-based pipeline were applied to measure global and regional perfusion. Volumetric regions of interest (ROIs) included GM, cerebral white matter, vascular territories, and the brain atlas from the UK Biobank. The cortical parcellation was using Desikan-Killiany atlas. Non-partial volume effect correction (PVEc) and PVEc GM-CBF changes with aging were modeled using linear regressions. Results: Global GM CBF decreased by 0.17mL/100g/min per year with aging before PVEc (p<0.05) and was 0.18mL/100g/min after PVEc (p<0.05). All cortical parcels exhibited CBF decreases with age before PVEc. After PVEc, seven parcels retained decreasing trends. However, GM CBF demonstrated increase with age after PVEc in three parcels. Conclusion: Although decreases in global perfusion are observed with aging before PVEc, perfusion variations appear to be more regionally selective after PVEc. This supports the understanding that variation in cerebral perfusion with age observed with imaging is influenced by regional changes in anatomy that can be accommodated with PVEc, but perfusion variation is still observable even after PVE is accounted for.
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页码:1807 / 1820
页数:14
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