Nomination of a novel plasma protein biomarker panel capable of classifying Alzheimer's disease dementia with high accuracy in an African American cohort
Lindsey A. KuchenbeckeriD, Kevin J. ThompsoniD, Cheyenne D. HurstiD, Bianca M. Opdenbosch, Michael G. HeckmaniD, Joseph S. ReddyiD, Thuy NguyeniD, Heidi L. CasellasiD, Katie D. Sotelo, Delila J. Reddy, John A. LucasiD, Gregory Scott DayiD, Floyd B. WillisiD, Neill R. Graff‐RadfordiD, Nilüfer Ertekin‐TaneriD, Krishna R. KalariiD, Minerva M. CarrasquilloiD
Abstract
IntroductionAfrican Americans (AA) are widely underrepresented in plasma biomarker studies for Alzheimers disease (AD) and current diagnostic biomarker candidates do not reflect the heterogeneity of AD. MethodsUntargeted proteome measurements were obtained using the SomaScan 7k platform to identify novel plasma biomarkers for AD in a cohort of AA clinically diagnosed as AD dementia (n=183) or cognitively unimpaired (CU, n=145). Machine learning approaches were implemented to identify the set of plasma proteins that yields the best classification accuracy. ResultsA plasma protein panel achieved an area under the curve (AUC) of 0.91 to classify AD dementia vs CU. The reproducibility of this finding was observed in the ANMerge plasma and AMP-AD Diversity brain datasets (AUC=0.83; AUC=0.94). DiscussionThis study demonstrates the potential of biomarker discovery through untargeted plasma proteomics and machine learning approaches. Our findings also highlight the potential importance of the matrisome and cerebrovascular dysfunction in AD pathophysiology.
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