Dementia after Ischemic Stroke, from Molecular Biomarkers to Therapeutic Options

被引:0
|
作者
Dammavalam, Vikalpa [1 ]
Rupert, Deborah [2 ]
Lanio, Marcos [1 ]
Jin, Zhaosheng [3 ]
Nadkarni, Neil [1 ]
Tsirka, Stella E. [4 ]
Bergese, Sergio D. [1 ]
机构
[1] Stony Brook Univ Hosp, Dept Neurol, Stony Brook, NY 11794 USA
[2] SUNY Stony Brook, Renaissance Sch Med, Stony Brook, NY 11794 USA
[3] Stony Brook Univ Hosp, Dept Anesthesiol, Stony Brook, NY 11794 USA
[4] SUNY Stony Brook, Renaissance Sch Med, Dept Pharmacol Sci, Stony Brook, NY 11794 USA
关键词
ischemic stroke; cognitive decline; dementia; biomarkers; novel therapy; VASCULAR COGNITIVE IMPAIRMENT; C-REACTIVE PROTEIN; WHITE-MATTER CHANGES; ANGIOTENSIN-CONVERTING ENZYME; TEMPORAL-LOBE ATROPHY; MINI-MENTAL-STATE; POSTSTROKE DEMENTIA; ALZHEIMERS-DISEASE; DOUBLE-BLIND; FUNCTIONAL RECOVERY;
D O I
10.3390/ijms25147772
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ischemic stroke is a leading cause of disability worldwide. While much of post-stroke recovery is focused on physical rehabilitation, post-stroke dementia (PSD) is also a significant contributor to poor functional outcomes. Predictive tools to identify stroke survivors at risk for the development of PSD are limited to brief screening cognitive tests. Emerging biochemical, genetic, and neuroimaging biomarkers are being investigated in an effort to unveil better indicators of PSD. Additionally, acetylcholinesterase inhibitors, NMDA receptor antagonists, dopamine receptor agonists, antidepressants, and cognitive rehabilitation are current therapeutic options for PSD. Focusing on the chronic sequelae of stroke that impair neuroplasticity highlights the need for continued investigative trials to better assess functional outcomes in treatments targeted for PSD.
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页数:22
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