Amino acid metabolomics and machine learning-driven assessment of future liver remnant growth after hepatectomy in livers of various backgrounds

IF 3.1 3区 医学 Q2 CHEMISTRY, ANALYTICAL Journal of pharmaceutical and biomedical analysis Pub Date : 2024-07-23 DOI:10.1016/j.jpba.2024.116369
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Abstract

Accurate assessment of future liver remnant growth after partial hepatectomy (PH) in patients with different liver backgrounds is a pressing clinical issue. Amino acid (AA) metabolism plays a crucial role in liver regeneration. In this study, we combined metabolomics and machine learning (ML) to develop a generalized future liver remnant assessment model for multiple liver backgrounds. The liver index was calculated at 0, 6, 24, 48, 72 and 168 h after 70 % PH in healthy mice and mice with nonalcoholic steatohepatitis or liver fibrosis. The serum levels of 39 amino acids (AAs) were measured using UPLC–MS/MS. The dataset was randomly divided into training and testing sets at a 2:1 ratio, and orthogonal partial least squares regression (OPLS) and minimally biased variable selection in R (MUVR) were used to select a metabolite signature of AAs. To assess liver remnant growth, nine ML models were built, and evaluated using the coefficient of determination (R2), mean absolute error (MAE), and root mean square error (RMSE). The post-Pareto technique for order preference by similarity to the ideal solution (TOPSIS) was employed for ranking the ML algorithms, and a stacking technique was utilized to establish consensus among the superior algorithms. Compared with those of OPLS, the signature AAs set identified by MUVR (Thr, Arg, EtN, Phe, Asa, 3MHis, Abu, Asp, Tyr, Leu, Ser, and bAib) are more concise. Post-Pareto TOPSIS ranking demonstrated that the majority of ML algorithm in combinations with MUVR outperformed those with OPLS. The established SVM-KNN consensus model performed best, with an R2 of 0.79, an MAE of 0.0029, and an RMSE of 0.0035 for the testing set. This study identified a metabolite signature of 12 AAs and constructed an SVM-KNN consensus model to assess future liver remnant growth after PH in mice with different liver backgrounds. Our preclinical study is anticipated to establish an alternative and generalized assessment method for liver regeneration.

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氨基酸代谢组学和机器学习驱动的对不同背景肝脏肝切除术后未来残肝生长的评估。
准确评估不同肝脏背景患者肝部分切除术(PH)后残余肝脏的未来生长情况是一个亟待解决的临床问题。氨基酸(AA)代谢在肝脏再生中起着至关重要的作用。在这项研究中,我们将代谢组学与机器学习(ML)相结合,建立了一个适用于多种肝脏背景的通用未来残肝评估模型。在健康小鼠和患有非酒精性脂肪性肝炎或肝纤维化的小鼠中,分别在70% PH后的0、6、24、48、72和168小时计算肝脏指数。使用 UPLC-MS/MS 测定了血清中 39 种氨基酸 (AA) 的水平。数据集以 2:1 的比例随机分为训练集和测试集,并使用正交偏最小二乘法回归(OPLS)和 R 中最小偏置变量选择(MUVR)来选择 AAs 代谢物特征。为了评估肝脏残余物的增长,建立了九个 ML 模型,并使用决定系数(R2)、平均绝对误差(MAE)和均方根误差(RMSE)进行评估。在对 ML 算法进行排序时,采用了与理想解相似的后帕累托排序偏好技术(TOPSIS),并利用堆叠技术在优势算法之间达成共识。与 OPLS 相比,MUVR 确定的特征 AA(Thr、Arg、EtN、Phe、Asa、3MHis、Abu、Asp、Tyr、Leu、Ser 和 bAib)更为简洁。帕雷托后 TOPSIS 排序表明,大多数 ML 算法与 MUVR 的组合优于与 OPLS 的组合。已建立的 SVM-KNN 共识模型表现最佳,测试集的 R2 为 0.79,MAE 为 0.0029,RMSE 为 0.0035。本研究确定了 12 种 AA 的代谢物特征,并构建了 SVM-KNN 共识模型,用于评估不同肝脏背景的小鼠 PH 后肝脏残余物的未来生长情况。我们的临床前研究有望为肝脏再生建立一种可供选择的通用评估方法。
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来源期刊
CiteScore
6.70
自引率
5.90%
发文量
588
审稿时长
37 days
期刊介绍: This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome. Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.
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