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Journal Article

Citation

Ruthirakuhan M, Lanctôt KL, Di Scipio M, Ahmed M, Herrmann N. Alzheimers Dement. 2018; 14(10): 1344-1376.

Affiliation

Hurvitz Brain Sciences Program, Sunnybrook Research Institute, Toronto, ON, USA; Geriatric Psychiatry, Sunnybrook Health Sciences Centre, Toronto, ON, USA; Department of Psychiatry, University of Toronto, Toronto, ON, USA. Electronic address: nathan.herrmann@sunnybrook.ca.

Copyright

(Copyright © 2018, Alzheimer's Association, Publisher Elsevier Publishing)

DOI

10.1016/j.jalz.2018.04.013

PMID

29940162

Abstract

INTRODUCTION: Agitation is one of the most challenging neuropsychiatric symptoms to treat in Alzheimer's disease and has significant implications for patient and caregiver. A major source of difficulty in identifying safe and effective treatments for agitation is the lack of validated biomarkers. As such, patients may not be appropriately targeted, and biological response to pharmacotherapy cannot be adequately monitored.

METHODS: This systematic review aimed to summarize evidence on the association between biomarkers and agitation/aggression in patients with Alzheimer's disease, utilizing the National Institute on Aging-Alzheimer's Association Research Framework and the Biomarkers, EndpointS, and other Tools Resource of the Food and Drug Association-National Institutes of Health Biomarker Working Group.

RESULTS: This review identified six classes of biomarkers (neuropathological, neurotransmitter, neuroimaging, apolipoprotein E (APOE) genotype, inflammatory, and clusterin) associated with agitation/aggression, which were mostly diagnostic in nature.

DISCUSSION: Future studies should investigate the predictive, prognostic, and monitoring capacity of biomarkers to provide insight into the longitudinal course of agitation/aggression, as well as predict and monitor biological response to a pharmacological intervention.

Copyright © 2018. Published by Elsevier Inc.


Language: en

Keywords

Aggression; Agitation; Alzheimer's disease; Amyloid; Biomarkers; Blood-based; Genetics; Neuroimaging; Neuropathology; Neurotransmitters; Tau

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