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DeepQA: A Unified Transcriptome-Based Aging Clock Using Deep Neural Networks

delete2025-01-05
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OA
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H
Hongqian Qi
H
Hongchen Zhao
E
Enyi Li
于宁波 cover
于宁波 (Ningbo Yu)
J
Jinchao Liu
韩建达 cover
韩建达 (Jianda Han) *
DOI:10.1111/acel.14471delete
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Abstract

Abstract

En 中文
Understanding the complex biological process of aging is of great value, especially as it can help develop therapeutics to prolong healthy life. Predicting biological age from gene expression data has shown to be an effective means to quantify aging of a subject, and to identify molecular and cellular biomarkers of aging. A typical approach for estimating biological age, adopted by almost all existing aging clocks, is to train machine learning models only on healthy subjects, but to infer on both healthy and unhealthy subjects. However, the inherent bias in this approach results in inaccurate biological age as shown in this study. Moreover, almost all existing transcriptome-based aging clocks were built around an inefficient procedure of gene selection followed by conventional machine learning models such as elastic nets, linear discriminant analysis etc. To address these limitations, we proposed DeepQA, a unified aging clock based on mixture of experts. Unlike existing methods, DeepQA is equipped with a specially designed Hinge-Mean-Absolute-Error (Hinge-MAE) loss so that it can train on both healthy and unhealthy subjects of multiple cohorts to reduce the bias of inferring biological age of unhealthy subjects. Our experiments showed that DeepQA significantly outperformed existing methods for biological age estimation on both healthy and unhealthy subjects. In addition, our method avoids the inefficient exhaustive search of genes, and provides a novel means to identify genes activated in aging prediction, alternative to such as differential gene expression analysis.
Keywords:
DISEASE
AGE
CELLS
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Journal

Aging Cell cover
Aging Cell
IF:
7.1
Papers:
3.7K
Citations:
1.9W

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nankai university
Scholars:
4.7W
Papers: 3.2W
Citations: 74