Explainable machine learning framework to predict personalized physiological aging

Author:

Bernard David12,Doumard Emmanuel1,Ader Isabelle1,Kemoun Philippe13,Pagès Jean‐Christophe14,Galinier Anne14,Cussat‐Blanc Sylvain25,Furger Felix1,Ferrucci Luigi6ORCID,Aligon Julien2,Delpierre Cyrille7,Pénicaud Luc1,Monsarrat Paul135ORCID,Casteilla Louis1

Affiliation:

1. RESTORE Research Center Université de Toulouse, INSERM 1301, CNRS 5070, EFS, ENVT France

2. Université Toulouse 1 – Capitole, Institute of Research in Informatics (IRIT) of Toulouse, CNRS Toulouse France

3. Oral Medicine Department and Hospital of Toulouse Toulouse Institute of Oral Medicine and Science, CHU de Toulouse Toulouse France

4. UFR Santé, Département Médecine, Institut Fédératif de Biologie, CHU de Toulouse Toulouse France

5. Artificial and Natural Intelligence Toulouse Institute ANITI Toulouse France

6. Biomedical Research Centre, National Institute on Aging NIH Baltimore Maryland USA

7. CERPOP, UMR1295 (Equity) Université P. Sabatier Toulouse France

Abstract

AbstractAttaining personalized healthy aging requires accurate monitoring of physiological changes and identifying subclinical markers that predict accelerated or delayed aging. Classic biostatistical methods most rely on supervised variables to estimate physiological aging and do not capture the full complexity of inter‐parameter interactions. Machine learning (ML) is promising, but its black box nature eludes direct understanding, substantially limiting physician confidence and clinical usage. Using a broad population dataset from the National Health and Nutrition Examination Survey (NHANES) study including routine biological variables and after selection of XGBoost as the most appropriate algorithm, we created an innovative explainable ML framework to determine a Personalized physiological age (PPA). PPA predicted both chronic disease and mortality independently of chronological age. Twenty‐six variables were sufficient to predict PPA. Using SHapley Additive exPlanations (SHAP), we implemented a precise quantitative associated metric for each variable explaining physiological (i.e., accelerated or delayed) deviations from age‐specific normative data. Among the variables, glycated hemoglobin (HbA1c) displays a major relative weight in the estimation of PPA. Finally, clustering profiles of identical contextualized explanations reveal different aging trajectories opening opportunities to specific clinical follow‐up. These data show that PPA is a robust, quantitative and explainable ML‐based metric that monitors personalized health status. Our approach also provides a complete framework applicable to different datasets or variables, allowing precision physiological age estimation.

Funder

Agence Nationale de la Recherche

Inserm transfert

European Regional Development Fund

Publisher

Wiley

Subject

Cell Biology,Aging

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3