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Motoric Cognitive Risk Syndrome: Predictor of Dementia and Age-Related Negative Outcomes
- Source :
- Frontiers in Medicine, Vol 4 (2017), Frontiers in Medicine
- Publication Year :
- 2017
- Publisher :
- Frontiers Media S.A., 2017.
-
Abstract
- Cognitive disorders represent a leading cause of disability in the aging population, of which dementia has the highest global burden. Early signs of dementia such as slow gait and memory complaints are known to present well before the overt manifestation of the disease. Motoric cognitive risk (MCR) syndrome characterized by the simultaneous presence of gait disturbances and memory complaints in older subjects has been proposed to study the close interactions between the physical and cognitive domains as well as a possible approach to identify individuals at increased risk of dementia. In addition, studies have shown MCR as a predictor of other negative outcomes in older adults, including disability, falls and death. However, the concept of MCR is still in its early stage and approach to the syndrome is still not well established. This review aims to put together the various aspects of MCR syndrome including its pathophysiology, diagnosis, epidemiology, and relationship with other geriatric conditions.
- Subjects :
- cognition
medicine.medical_specialty
Population ageing
Mini Review
motoric cognitive risk
Disease
gait
03 medical and health sciences
0302 clinical medicine
Age related
Epidemiology
medicine
Dementia
030212 general & internal medicine
Psychiatry
geriatric disorders
lcsh:R5-920
business.industry
Gait Disturbance
Cognition
General Medicine
medicine.disease
Gait
subjective memory complaint
Medicine
business
lcsh:Medicine (General)
030217 neurology & neurosurgery
hormones, hormone substitutes, and hormone antagonists
Clinical psychology
dementia
Subjects
Details
- Language :
- English
- Volume :
- 4
- Database :
- OpenAIRE
- Journal :
- Frontiers in Medicine
- Accession number :
- edsair.doi.dedup.....b8705d5e880806feb7eb4314f7d271b4
- Full Text :
- https://doi.org/10.3389/fmed.2017.00166/full