Searching for just a few words should be enough to get started. If you need to make more complex queries, use the tips below to guide you.
Article type: Research Article
Authors: Nagaraja, Nandakumara; 1; * | Wang, Wei-enb | Duara, Ranjanc | DeKosky, Steven T.a; d | Vaillancourt, Davidb; e
Affiliations: [a] Department of Neurology, College of Medicine, University of Florida, Gainesville, FL, USA | [b] Laboratory for Rehabilitation Neuroscience, Department of Applied Physiology and Kinesiology, University of Florida, Gainesville, FL, USA | [c] Department of Neurology, Mount Sinai Medical Center, Miami Beach, FL, USA | [d] McKnight Brain Institute, University of Florida, Gainesville, FL, USA | [e] Department of Biomedical Engineering, University of Florida, Gainesville, FL, USA
Correspondence: [*] Correspondence to: Nandakumar Nagaraja, MD, MS, FAHA, Department of Neurology, Penn State College of Medicine, Milton S. Hershey Medical Center, 30 Hope Drive, Suite 2800, PO Box 859, EC037, Hershey, PA 17033, USA. Tel.: +1 717 531 0003 /Ext 289694; Fax: +1 717 531 0384; E-mail: [email protected].
Note: [1] Present address: Department of Neurology, Penn State College of Medicine, Milton S. Hershey Medical Center, Hershey, PA, USA.
Abstract: Background:Hippocampal atrophy in cerebral amyloid angiopathy (CAA) has been reported to be similar to that in Alzheimer’s disease (AD). Objective:To evaluate if CAA pathology partly mediates reduced hippocampal volume in patients with AD. Methods:Patients with a clinical diagnosis of AD and neuropathological confirmation of AD+/-CAA in the National Alzheimer’s Coordinating Center database were included in the study. The volumes of temporal lobe structures were calculated on T1-weighted imaging (T1-MRI) using automated FreeSurfer software, from images acquired on average 5 years prior to death. Multivariate regression analysis was performed to compare brain volumes in four CAA groups. The hippocampal volume on T1-MRI was correlated with Clinical Dementia Rating sum of boxes (CDRsb) score, apolipoprotein E (APOE) genotype, and hippocampal atrophy at autopsy. Results:The study included 231 patients with no (n = 45), mild (n = 70), moderate (n = 67), and severe (n = 49) CAA. Among the four CAA groups, patients with severe CAA had a smaller mean left hippocampal volume (p = 0.023) but this was not significant when adjusted for APOE ɛ4 (p = 0.07). The left hippocampal volume on MRI correlated significantly with the hippocampal atrophy grading on neuropathology (p = 0.0003). Among patients with severe CAA, the left hippocampal volume on T1-MRI: (a) decreased with an increase in the number of APOE ɛ4 alleles (p = 0.04); but (b) had no evidence of correlation with CDRsb score (p = 0.57). Conclusion:Severe CAA was associated with smaller left hippocampal volume on T1-MRI up to five years prior to death among patients with neuropathologically confirmed AD. This relationship was dependent on APOE ɛ4 genotype.
Keywords: Alzheimer’s disease, trophy, cerebral amyloid angiopathy, hippocampus
DOI: 10.3233/JAD-220624
Journal: Journal of Alzheimer's Disease, vol. 93, no. 2, pp. 495-507, 2023
IOS Press, Inc.
6751 Tepper Drive
Clifton, VA 20124
USA
Tel: +1 703 830 6300
Fax: +1 703 830 2300
[email protected]
For editorial issues, like the status of your submitted paper or proposals, write to [email protected]
IOS Press
Nieuwe Hemweg 6B
1013 BG Amsterdam
The Netherlands
Tel: +31 20 688 3355
Fax: +31 20 687 0091
[email protected]
For editorial issues, permissions, book requests, submissions and proceedings, contact the Amsterdam office [email protected]
Inspirees International (China Office)
Ciyunsi Beili 207(CapitaLand), Bld 1, 7-901
100025, Beijing
China
Free service line: 400 661 8717
Fax: +86 10 8446 7947
[email protected]
For editorial issues, like the status of your submitted paper or proposals, write to [email protected]
如果您在出版方面需要帮助或有任何建, 件至: [email protected]