Potential Therapeutic Approaches for Cerebral Amyloid Angiopathy and Alzheimer’s Disease

Cerebral amyloid angiopathy (CAA) is a cerebrovascular disease directly implicated in Alzheimer’s disease (AD) pathogenesis through amyloid-β (Aβ) deposition, which may cause the development and progression of dementia. Despite extensive studies to explore drugs targeting...

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Main Authors: Masashi Tanaka, Satoshi Saito, Takayuki Inoue, Noriko Satoh-Asahara, Masafumi Ihara
Format: Article
Language:English
Published: MDPI AG 2020-03-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/21/6/1992
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spelling doaj-f99ce6c50a924544af7e31a78bb5a71a2020-11-25T01:54:55ZengMDPI AGInternational Journal of Molecular Sciences1422-00672020-03-01216199210.3390/ijms21061992ijms21061992Potential Therapeutic Approaches for Cerebral Amyloid Angiopathy and Alzheimer’s DiseaseMasashi Tanaka0Satoshi Saito1Takayuki Inoue2Noriko Satoh-Asahara3Masafumi Ihara4Department of Physical Therapy, Health Science University, 7187 Kodachi, Fujikawaguchiko-machi, Minamitsuru-gun, Yamanashi 401-0380, JapanDepartment of Neurology, National Cerebral and Cardiovascular Center, 6-1 Kishibe-Shimmachi, Suita, Osaka 564-8565, JapanDepartment of Endocrinology, Metabolism, and Hypertension Research, Clinical Research Institute, National Hospital Organization Kyoto Medical Center, 1-1 Fukakusa Mukaihata-cho, Fushimi-ku, Kyoto 612-8555, JapanDepartment of Endocrinology, Metabolism, and Hypertension Research, Clinical Research Institute, National Hospital Organization Kyoto Medical Center, 1-1 Fukakusa Mukaihata-cho, Fushimi-ku, Kyoto 612-8555, JapanDepartment of Neurology, National Cerebral and Cardiovascular Center, 6-1 Kishibe-Shimmachi, Suita, Osaka 564-8565, JapanCerebral amyloid angiopathy (CAA) is a cerebrovascular disease directly implicated in Alzheimer’s disease (AD) pathogenesis through amyloid-β (Aβ) deposition, which may cause the development and progression of dementia. Despite extensive studies to explore drugs targeting Aβ, clinical benefits have not been reported in large clinical trials in AD patients or presymptomatic individuals at a risk for AD. However, recent studies on CAA and AD have provided novel insights regarding CAA- and AD-related pathogenesis. This work has revealed potential therapeutic targets, including Aβ drainage pathways, Aβ aggregation, oxidative stress, and neuroinflammation. The functional significance and therapeutic potential of bioactive molecules such as cilostazol and taxifolin have also become increasingly evident. Furthermore, recent epidemiological studies have demonstrated that serum levels of a soluble form of triggering receptor expressed on myeloid cells 2 (TREM2) may have clinical significance as a potential novel predictive biomarker for dementia incidence. This review summarizes recent advances in CAA and AD research with a focus on discussing future research directions regarding novel therapeutic approaches and predictive biomarkers for CAA and AD.https://www.mdpi.com/1422-0067/21/6/1992alzheimer’s diseaseamyloid-βantioxidantscerebral amyloid angiopathycilostazolglycationinflammationintramural peri-arterial drainagetaxifolintriggering receptor expressed on myeloid cells 2
collection DOAJ
language English
format Article
sources DOAJ
author Masashi Tanaka
Satoshi Saito
Takayuki Inoue
Noriko Satoh-Asahara
Masafumi Ihara
spellingShingle Masashi Tanaka
Satoshi Saito
Takayuki Inoue
Noriko Satoh-Asahara
Masafumi Ihara
Potential Therapeutic Approaches for Cerebral Amyloid Angiopathy and Alzheimer’s Disease
International Journal of Molecular Sciences
alzheimer’s disease
amyloid-β
antioxidants
cerebral amyloid angiopathy
cilostazol
glycation
inflammation
intramural peri-arterial drainage
taxifolin
triggering receptor expressed on myeloid cells 2
author_facet Masashi Tanaka
Satoshi Saito
Takayuki Inoue
Noriko Satoh-Asahara
Masafumi Ihara
author_sort Masashi Tanaka
title Potential Therapeutic Approaches for Cerebral Amyloid Angiopathy and Alzheimer’s Disease
title_short Potential Therapeutic Approaches for Cerebral Amyloid Angiopathy and Alzheimer’s Disease
title_full Potential Therapeutic Approaches for Cerebral Amyloid Angiopathy and Alzheimer’s Disease
title_fullStr Potential Therapeutic Approaches for Cerebral Amyloid Angiopathy and Alzheimer’s Disease
title_full_unstemmed Potential Therapeutic Approaches for Cerebral Amyloid Angiopathy and Alzheimer’s Disease
title_sort potential therapeutic approaches for cerebral amyloid angiopathy and alzheimer’s disease
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2020-03-01
description Cerebral amyloid angiopathy (CAA) is a cerebrovascular disease directly implicated in Alzheimer’s disease (AD) pathogenesis through amyloid-β (Aβ) deposition, which may cause the development and progression of dementia. Despite extensive studies to explore drugs targeting Aβ, clinical benefits have not been reported in large clinical trials in AD patients or presymptomatic individuals at a risk for AD. However, recent studies on CAA and AD have provided novel insights regarding CAA- and AD-related pathogenesis. This work has revealed potential therapeutic targets, including Aβ drainage pathways, Aβ aggregation, oxidative stress, and neuroinflammation. The functional significance and therapeutic potential of bioactive molecules such as cilostazol and taxifolin have also become increasingly evident. Furthermore, recent epidemiological studies have demonstrated that serum levels of a soluble form of triggering receptor expressed on myeloid cells 2 (TREM2) may have clinical significance as a potential novel predictive biomarker for dementia incidence. This review summarizes recent advances in CAA and AD research with a focus on discussing future research directions regarding novel therapeutic approaches and predictive biomarkers for CAA and AD.
topic alzheimer’s disease
amyloid-β
antioxidants
cerebral amyloid angiopathy
cilostazol
glycation
inflammation
intramural peri-arterial drainage
taxifolin
triggering receptor expressed on myeloid cells 2
url https://www.mdpi.com/1422-0067/21/6/1992
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