| Literature DB >> 28188032 |
Stéphane Epelbaum1, Rémy Genthon2, Enrica Cavedo2, Marie Odile Habert3, Foudil Lamari4, Geoffroy Gagliardi5, Simone Lista6, Marc Teichmann5, Hovagim Bakardjian6, Harald Hampel7, Bruno Dubois5.
Abstract
Preclinical Alzheimer's disease (AD) is a relatively recent concept describing an entity characterized by the presence of a pathophysiological biomarker signature characteristic for AD in the absence of specific clinical symptoms. There is rising interest in the scientific community to define such an early target population mainly because of failures of all recent clinical trials despite evidence of biological effects on brain amyloidosis for some compounds. A conceptual framework has recently been proposed for this preclinical phase of AD. However, few data exist on this silent stage of AD. We performed a systematic review to investigate how the concept is defined across studies. The review highlights the substantial heterogeneity concerning the three main determinants of preclinical AD: "normal cognition," "cognitive decline," and "AD pathophysiological signature." We emphasize the need for a harmonized nomenclature of the preclinical AD concept and standardized population-based and case-control studies using unified operationalized criteria.Entities:
Keywords: Biomarker; Clinical trial; Cognition; Cohort; Cross-sectional; Familial Alzheimer's disease; Longitudinal; Neuropathology; Preclinical Alzheimer's disease; Systematic review
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Year: 2017 PMID: 28188032 DOI: 10.1016/j.jalz.2016.12.003
Source DB: PubMed Journal: Alzheimers Dement ISSN: 1552-5260 Impact factor: 21.566