| Literature DB >> 27702618 |
Marion Mortamais1, Jessica A Ash2, John Harrison3, Jeffrey Kaye4, Joel Kramer5, Christopher Randolph6, Carine Pose7, Bruce Albala8, Michael Ropacki9, Craig W Ritchie10, Karen Ritchie11.
Abstract
Significant progress has been made in characterizing the biological changes occurring in preclinical Alzheimer's disease (AD). Cognitive dysfunction has been viewed, however, as a late-stage phenomenon, despite increasing evidence that changes may be detected in the decades preceding dementia. In the absence of comprehensive evidence-based guidelines for preclinical cognitive assessment, longitudinal cohort and neuroimaging studies have been reviewed to determine the temporal order and brain biomarker correlates of specific cognitive functions. Episodic memory decline was observed to be the most salient cognitive function, correlating with high levels of amyloid deposition and hypoconnectivity across large-scale brain networks. Prospective studies point to early decline in both episodic and semantic memory processing as well as executive functions in the predementia period. The cognitive tests have, however, been principally those used to diagnose dementia. New procedures are required which target more finely the medial temporal lobe subregions first affected by clinically silent AD pathology.Entities:
Keywords: Alzheimer's disease; Cognition; Diagnosis; Neuropsychology; Preclinical markers
Mesh:
Year: 2016 PMID: 27702618 DOI: 10.1016/j.jalz.2016.06.2365
Source DB: PubMed Journal: Alzheimers Dement ISSN: 1552-5260 Impact factor: 21.566