Journal article
P50: A candidate ERP biomarker of prodromal Alzheimer's disease
Brain research, v 1624, pp 390-397
22 Oct 2015
PMID: 26256251
Featured in Collection : UN Sustainable Development Goals @ Drexel
Abstract
Reductions of cerebrospinal fluid (CSF) amyloid-beta (Aβ42) and elevated phosphorylated-tau (p-Tau) reflect in vivo Alzheimer's disease (AD) pathology and show utility in predicting conversion from mild cognitive impairment (MCI) to dementia. We investigated the P50 event-related potential component as a noninvasive biomarker of AD pathology in non-demented elderly.
36 MCI patients were stratified into amyloid positive (MCI-AD, n=17) and negative (MCI-Other, n=19) groups using CSF levels of Aβ42. All amyloid positive patients were also p-Tau positive. P50s were elicited with an auditory oddball paradigm.
MCI-AD patients yielded larger P50s than MCI-Other. The best amyloid-status predictor model showed 94.7% sensitivity, 94.1% specificity and 94.4% total accuracy.
P50 predicted amyloid status in MCI patients, thereby showing a relationship with AD pathology versus MCI from another etiology. The P50 may have clinical utility for inexpensive pre-screening and assessment of Alzheimer's pathology.
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Details
- Title
- P50: A candidate ERP biomarker of prodromal Alzheimer's disease
- Creators
- Deborah L Green - Drexel UniversityLisa Payne - Brandeis UniversityRobi Polikar - Rowan UniversityPaul J Moberg - University of PennsylvaniaDavid A Wolk - University of PennsylvaniaJohn Kounios - Drexel University
- Publication Details
- Brain research, v 1624, pp 390-397
- Publisher
- Elsevier
- Grant note
- P30 AG010124 / NIA NIH HHS
- Resource Type
- Journal article
- Language
- English
- Academic Unit
- Psychological and Brain Sciences (Psychology)
- Web of Science ID
- WOS:000365050100039
- Scopus ID
- 2-s2.0-84954285919
- Other Identifier
- 991019168770404721
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- Collaboration types
- Domestic collaboration
- Web of Science research areas
- Neurosciences