Deep learning approach to parameter optimization for physiological models.

Xiaoyu Duan, Vipul Periwal
{"title":"Deep learning approach to parameter optimization for physiological models.","authors":"Xiaoyu Duan, Vipul Periwal","doi":"10.1101/2025.02.25.639944","DOIUrl":null,"url":null,"abstract":"<p><p>The inference of nonlinear dynamics and parameters in biological data modeling is challenging. Conventional methodologies, based on hypothetical underlying mechanisms, complicate inference because standard parameter optimization methods are difficult to constrain to biological ranges. Here, we propose a novel method to evaluate and improve putative models using neural networks to simultaneously address biological modeling, parametrization, and parameter inference. As an example, utilizing data from clinical frequently sampled intravenous glucose tolerance testing, we introduce two physiological lipolysis models (with parameters) of the dynamics of glucose, insulin, and free fatty acids (FFA). Parameter values are obtained via optimization from the limited clinical data. We then generate large quantities of simulated data from the model by sampling parameters within physiological ranges. A convolutional neural network is trained to take the simulated data time courses of glucose, insulin, and FFA as input and output the model parameters. The performance of the trained neural network is evaluated for both parameter inference and reconstruction of trajectories over a testing dataset and from optimized model-fitting curves. We show that our methodology enables accurate parameter inference and trajectory reconstruction over the testing dataset and optimized model-fitting curves. The trained neural network produces consistently high <math> <msup><mrow><mi>R</mi></mrow> <mrow><mn>2</mn></mrow> </msup> </math> values and low <math><mi>p</mi></math> -values across different feature engineering strategies and training dataset sizes. We assess the impact of feature engineering choices and training dataset size on inference performance, demonstrating that appropriately designed feature transformations and certain activation function improve accuracy. Our results establish a deep learning framework for parameter inference in mathematical models, which can be adapted to various physiological systems.</p>","PeriodicalId":519960,"journal":{"name":"bioRxiv : the preprint server for biology","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-02-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11888287/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"bioRxiv : the preprint server for biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2025.02.25.639944","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The inference of nonlinear dynamics and parameters in biological data modeling is challenging. Conventional methodologies, based on hypothetical underlying mechanisms, complicate inference because standard parameter optimization methods are difficult to constrain to biological ranges. Here, we propose a novel method to evaluate and improve putative models using neural networks to simultaneously address biological modeling, parametrization, and parameter inference. As an example, utilizing data from clinical frequently sampled intravenous glucose tolerance testing, we introduce two physiological lipolysis models (with parameters) of the dynamics of glucose, insulin, and free fatty acids (FFA). Parameter values are obtained via optimization from the limited clinical data. We then generate large quantities of simulated data from the model by sampling parameters within physiological ranges. A convolutional neural network is trained to take the simulated data time courses of glucose, insulin, and FFA as input and output the model parameters. The performance of the trained neural network is evaluated for both parameter inference and reconstruction of trajectories over a testing dataset and from optimized model-fitting curves. We show that our methodology enables accurate parameter inference and trajectory reconstruction over the testing dataset and optimized model-fitting curves. The trained neural network produces consistently high R 2 values and low p -values across different feature engineering strategies and training dataset sizes. We assess the impact of feature engineering choices and training dataset size on inference performance, demonstrating that appropriately designed feature transformations and certain activation function improve accuracy. Our results establish a deep learning framework for parameter inference in mathematical models, which can be adapted to various physiological systems.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
生理模型参数优化的深度学习方法。
生物数据建模中非线性动力学和参数的推断具有挑战性。传统的方法,基于假设的潜在机制,使推理复杂化,因为标准参数优化方法难以约束在生物范围内。在这里,我们提出了一种新的方法来评估和改进假设模型,使用神经网络同时解决生物建模,参数化和参数推理。作为一个例子,我们利用临床频繁采样的静脉葡萄糖耐量试验数据,介绍了葡萄糖、胰岛素和游离脂肪酸(FFA)动态的两种生理脂肪分解模型(带参数)。参数值是通过优化有限的临床数据得到的。然后,我们通过在生理范围内的采样参数从模型中生成大量模拟数据。训练卷积神经网络,以模拟葡萄糖、胰岛素和FFA的数据时间过程作为模型参数的输入和输出。通过测试数据集和优化的模型拟合曲线来评估训练后的神经网络的性能,包括参数推理和轨迹重建。我们表明,我们的方法能够在测试数据集和优化的模型拟合曲线上实现准确的参数推断和轨迹重建。经过训练的神经网络在不同的特征工程策略和训练数据集大小中产生一致的高r2值和低p值。我们评估了特征工程选择和训练数据集大小对推理性能的影响,证明了适当设计的特征转换和一定的激活函数可以提高准确率。我们的研究结果为数学模型中的参数推理建立了一个深度学习框架,该框架可以适应各种生理系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Coarse-Grained Simulations of Mycobacterial Outer Membranes Reveal Fluidity-Dependent PDIM Redistribution Across Different Lipid Environments. Process for Standardizing and Assessing the Parameters Governing MS2 Virus-Like Particle Reassembly around Nucleic Acid Cargo. Next generation protein-corrole bio-assemblies provide effective tumoricidal treatment in a metastatic triple-negative breast cancer model. Rapid Histone Post-Translational Modification Analysis Using Alternative Proteases and Tandem Mass Tags. HDAC5 -encoded Microprotein NISM Mediates Nucleolar Formation and Ribosomal RNA Synthesis.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1