| NEUROBIOLOGY OF AGING | 卷:76 |
| Increased cerebral blood volume in small arterial vessels is a correlate of amyloid-β-related cognitive decline | |
| Article | |
| Hua, Jun1,2  Lee, SeungWook3  Blair, Nicholas I. S.3  Wyss, Michael4,5  van Bergen, Jiri M. G.6  Schreiner, Simon J.6,7  Kagerer, Sonja M.6,7  Leh, Sandra E.6  Gietl, Anton E.6  Treyer, Valerie6,8  Buck, Alfred8  Nitsch, Roger M.6  Pruessmann, Klaas P.4,5  Lu, Hanzhang1,2  Van Zijl, Peter C. M.1,2  Albert, Marilyn9  Hock, Christoph6  Unschuld, Paul G.6,7  | |
| [1] Johns Hopkins Univ, Sch Med, Dept Radiol, Neurosect,Div MRI Res, Baltimore, MD 21205 USA | |
| [2] Kennedy Krieger Inst, FM Kirby Res Ctr Funct Brain Imaging, Baltimore, MD USA | |
| [3] Johns Hopkins Univ, Dept Biomed Engn, Baltimore, MD USA | |
| [4] Univ Zurich, Inst Biomed Engn, Zurich, Switzerland | |
| [5] Swiss Fed Inst Technol, Zurich, Switzerland | |
| [6] Univ Zurich, Inst Regenerat Med IREM, Schlieren, Switzerland | |
| [7] Psychiat Univ Hosp Zurich PUK, Hosp Psychogeriatr Med, Zurich, Switzerland | |
| [8] Univ Hosp Zurich, Dept Nucl Med, Zurich, Switzerland | |
| [9] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21205 USA | |
| 关键词: MRI; PET; CBV; 7 Tesla; Imaging; Biomarker; Vascular; Perfusion; High field; Aging; Cerebral autoregulation; Alzheimer's disease; | |
| DOI : 10.1016/j.neurobiolaging.2019.01.001 | |
| 来源: Elsevier | |
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【 摘 要 】
The protracted accumulation of amyloid-beta (A beta) is a major pathologic hallmark of Alzheimer's disease and may trigger secondary pathological processes that include neurovascular damage. This study was aimed at investigating long-term effects of A beta burden on cerebral blood volume of arterioles and pial arteries (CBVa), possibly present before manifestation of dementia. A beta burden was assessed by 11C Pittsburgh compound-B positron emission tomography in 22 controls and 18 persons with mild cognitive impairment (MCI), [ages: 75(+/-6) years]. After 2 years, inflow-based vascular space occupancy at ultra-high field strength of 7-Tesla was administered for measuring CBVa, and neuropsychological testing for cognitive decline. Crushing gradients were incorporated during MR-imaging to suppress signals from fast-flowing blood in large arteries, and thereby sensitize inflow-based vascular space occupancy to CBVa in pial arteries and arterioles. CBVa was significantly elevated in MCI compared to cognitively normal controls and regional CBVa related to local A beta deposition. For both MCI and controls, A beta burden and follow-up CBVa in several brain regions synergistically predicted cognitive decline over 2 years. Orbitofrontal CBVa was positively associated with apolipoprotein E e4 carrier status. Increased CBVa may reflect long-term effects of region-specific pathology associated with A beta deposition. Additional studies are needed to clarify the role of the arteriolar system and the potential of CBVa as a biomarker for A beta-related vascular downstream pathology. (C) 2019 The Authors. Published by Elsevier Inc.
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| 10_1016_j_neurobiolaging_2019_01_001.pdf | 1761KB |
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