Deep biomarkers of human aging: Application of deep neural networks to biomarker development

Evgeny Putin(ITMO University), Polina Mamoshina(Urology Foundation), Alexander Aliper(Insilico Medicine (United States)), Mikhail Korzinkin(Insilico Medicine (United States)), Alexey Moskalev(George Mason University), Alexey Kolosov, Alexander Ostrovskiy, Charles R. Cantor(Boston University), Jan Vijg(Albert Einstein College of Medicine), Alex Zhavoronkov(Urology Foundation)
Aging
May 18, 2016
Cited by 376Open Access
Full Text

Abstract

One of the major impediments in human aging research is the absence of a comprehensive and actionable set of biomarkers that may be targeted and measured to track the effectiveness of therapeutic interventions. In this study, we designed a modular ensemble of 21 deep neural networks (DNNs) of varying depth, structure and optimization to predict human chronological age using a basic blood test. To train the DNNs, we used over 60,000 samples from common blood biochemistry and cell count tests from routine health exams performed by a single laboratory and linked to chronological age and sex. The best performing DNN in the ensemble demonstrated 81.5 % epsilon-accuracy r = 0.90 with R(2) = 0.80 and MAE = 6.07 years in predicting chronological age within a 10 year frame, while the entire ensemble achieved 83.5% epsilon-accuracy r = 0.91 with R(2) = 0.82 and MAE = 5.55 years. The ensemble also identified the 5 most important markers for predicting human chronological age: albumin, glucose, alkaline phosphatase, urea and erythrocytes. To allow for public testing and evaluate real-life performance of the predictor, we developed an online system available at http://www.aging.ai. The ensemble approach may facilitate integration of multi-modal data linked to chronological age and sex that may lead to simple, minimally invasive, and affordable methods of tracking integrated biomarkers of aging in humans and performing cross-species feature importance analysis.


Related Papers

No related papers found

Powered by citation graph analysis