Abstract
Research criteria for Alzheimer's disease recommend the use of biomarkers for diagnosis, but whether biomarkers improve the diagnosis in clinical routine has not been systematically assessed. The aim is to evaluate the evidence for use of medial temporal lobe atrophy (MTA) as a biomarker for Alzheimer's disease at the mild cognitive impairment stage in routine clinical practice, with an adapted version of the 5-phase oncology framework for biomarker development. A literature review on visual assessment of MTA and hippocampal volumetry was conducted with other biomarkers addressed in parallel reviews. Ample evidence is available for phase 1 (rationale for use) and phase 2 (discriminative ability between diseased and control subjects). Phase 3 (early detection ability) is partly achieved: most evidence is derived from research cohorts or clinical populations with short follow-up, but validation in clinical mild cognitive impairment cohorts is required. In phase 4, only the practical feasibility has been addressed for visual rating of MTA. The rest of phase 4 and phase 5 have not yet been addressed. (C) 2016 Elsevier Inc. All rights reserved.
Original language | English |
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Pages (from-to) | 167-182 |
Number of pages | 16 |
Journal | Neurobiology of Aging |
Volume | 52 |
DOIs | |
Publication status | Published - Apr 2017 |
Keywords
- Alzheimer's disease
- Dementia
- Mild cognitive impairment
- Hippocampus
- Medial temporal lobe atrophy
- MRI
- Roadmap
- MILD COGNITIVE IMPAIRMENT
- ADNI HARMONIZED PROTOCOL
- REGISTERED SERIAL MRI
- VASCULAR RISK-FACTORS
- VISUAL RATING-SCALES
- LOBE ATROPHY
- HIPPOCAMPAL VOLUME
- MAGNETIC-RESONANCE
- APOLIPOPROTEIN-E
- FRONTOTEMPORAL DEMENTIA