A two-stage neural network prediction of chronic kidney disease

IF 1.9 4区 生物学 Q4 CELL BIOLOGY IET Systems Biology Pub Date : 2021-06-29 DOI:10.1049/syb2.12031
Hongquan Peng, Haibin Zhu, Chi Wa Ao Ieong, Tao Tao, Tsung Yang Tsai, Zhi Liu
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引用次数: 4

Abstract

Accurate detection of chronic kidney disease (CKD) plays a pivotal role in early diagnosis and treatment. Measured glomerular filtration rate (mGFR) is considered the benchmark indicator in measuring the kidney function. However, due to the high resource cost of measuring mGFR, it is usually approximated by the estimated glomerular filtration rate, underscoring an urgent need for more precise and stable approaches. With the introduction of novel machine learning methodologies, prediction performance is shown to be significantly improved across all available data, but the performance is still limited because of the lack of models in dealing with ultra-high dimensional datasets. This study aims to provide a two-stage neural network approach for prediction of GFR and to suggest some other useful biomarkers obtained from the blood metabolites in measuring GFR. It is a composite of feature shrinkage and neural network when the number of features is much larger than the number of training samples. The results show that the proposed method outperforms the existing ones, such as convolutionneural network and direct deep neural network.

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慢性肾脏疾病的两阶段神经网络预测
准确检测慢性肾脏疾病(CKD)在早期诊断和治疗中起着关键作用。测量肾小球滤过率(mGFR)被认为是衡量肾功能的基准指标。然而,由于测量mGFR的资源成本高,它通常由估计的肾小球滤过率来近似,这强调了迫切需要更精确和稳定的方法。随着新的机器学习方法的引入,所有可用数据的预测性能都得到了显着提高,但由于缺乏处理超高维数据集的模型,性能仍然受到限制。本研究旨在提供一种两阶段神经网络方法来预测GFR,并建议在测量GFR时从血液代谢物中获得一些其他有用的生物标志物。当特征的数量远远大于训练样本的数量时,它是特征收缩和神经网络的复合。结果表明,该方法优于现有的卷积神经网络和直接深度神经网络。
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来源期刊
IET Systems Biology
IET Systems Biology 生物-数学与计算生物学
CiteScore
4.20
自引率
4.30%
发文量
17
审稿时长
>12 weeks
期刊介绍: IET Systems Biology covers intra- and inter-cellular dynamics, using systems- and signal-oriented approaches. Papers that analyse genomic data in order to identify variables and basic relationships between them are considered if the results provide a basis for mathematical modelling and simulation of cellular dynamics. Manuscripts on molecular and cell biological studies are encouraged if the aim is a systems approach to dynamic interactions within and between cells. The scope includes the following topics: Genomics, transcriptomics, proteomics, metabolomics, cells, tissue and the physiome; molecular and cellular interaction, gene, cell and protein function; networks and pathways; metabolism and cell signalling; dynamics, regulation and control; systems, signals, and information; experimental data analysis; mathematical modelling, simulation and theoretical analysis; biological modelling, simulation, prediction and control; methodologies, databases, tools and algorithms for modelling and simulation; modelling, analysis and control of biological networks; synthetic biology and bioengineering based on systems biology.
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