4.6 Article

Aging-related markers in rat urine revealed by dynamic metabolic profiling using machine learning

期刊

AGING-US
卷 13, 期 10, 页码 14322-14341

出版社

IMPACT JOURNALS LLC
DOI: 10.18632/aging.203046

关键词

aging; metabolic trajectories; biomarkers; time-series; machine learning

资金

  1. National Natural Science Foundation of China [81973035]
  2. Applied Technology Research and Development Plan of Heilongjiang Province [GA20C012]
  3. Chinese Nutrition Society-Yihai Kerry Nutrition and Safety Research Foundation [CNS-W2018A41]

向作者/读者索取更多资源

The study identified reliable markers related to aging through machine learning, using metabolomic profiles generated from rat urine. These markers were validated in different age groups and can potentially be used as therapeutic antiaging targets.
The process of aging and metabolism is intimately intertwined; thus, developing biomarkers related to metabolism is critical for delaying aging. However, few studies have identified reliable markers that reflect aging trajectories based on machine learning. We generated metabolomic profiles from rat urine using ultra-performance liquid chromatography/mass spectrometry. This was dynamically collected at four stages of the rat's age (20, 50, 75, and 100 weeks) for both the training and test groups. Partial least squares-discriminant analysis score plots revealed a perfect separation trajectory in one direction with increasing age in the training and test groups. We further screened 25 aging-related biomarkers through the combination of four algorithms (VIP, time-series, LASSO, and SVM-RFE) in the training group. They were validated in the test group with an area under the curve of 1. Finally, six metabolites, known or novel aging-related markers, were identified, including epinephrine, glutarylcarnitine, L-kynurenine, taurine, 3-hydroxydodecanedioic acid, and N-acetylcitrulline. We also found that, except for N-acetylcitrulline (p < 0.05), the identified aging-related metabolites did not differ between tumor-free and tumor-bearing rats at 100 weeks (p > 0.05). Our findings reveal the metabolic trajectories of aging and provide novel biomarkers as potential therapeutic antiaging targets.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据