Huang Xin, Zhou Yang, Tang Haoze, Liu Bing, Su Benzhe, Wang Qi
School of Mathematics and Information Science, Anshan Normal University, Anshan, 114007, China.
Liaoning Clinical Research Center for Lung Cancer, the Second Hospital of Dalian Medical University, Dalian, 116023, China.
J Biomed Inform. 2021 Jun;118:103796. doi: 10.1016/j.jbi.2021.103796. Epub 2021 Apr 29.
Individual variation in genetic and environmental factors can cause the differences in metabolic phenotypes, which may have an effect on drug responses of patients. Deep exploration of patients' responses to therapeutic agents is a crucial and urgent event in the personalized treatment study. Using machine learning methods for the discovery of suitability evaluation biomarkers can provide deep insight into the mechanism of disease therapy and facilitate the development of personalized medicine. To find important metabolic network signals for the prediction of patients' drug responses, a novel method referred to as differential metabolic network construction (DMNC) was proposed. In DMNC, concentration changes in metabolite ratios between different pathological states are measured to construct differential metabolic networks, which can be used to advance clinical decision-making. In this study, DMNC was applied to characterize type 2 diabetes mellitus (T2DM) patients' responses against gliclazide modified-release (MR) therapy. Two T2DM metabolomics datasets from different batches of subjects treated by gliclazide MR were analyzed in depth. A network biomarker was defined to assess the patients' suitability for gliclazide MR. It can be effective in the prediction of significant responders from nonsignificant responders, achieving area under the curve values of 0.893 and 1.000 for the discovery and validation sets, respectively. Compared with the metabolites selected by the other methods, the network biomarker selected by DMNC was more stable and precise to reflect the metabolic responses in patients to gliclazide MR therapy, thereby contributing for the personalized medicine of T2DM patients. The better performance of DMNC validated its potential for the identification of network biomarkers to characterize the responses against therapeutic treatments and provide valuable information for personalized medicine.
遗传和环境因素的个体差异会导致代谢表型的不同,这可能会影响患者的药物反应。深入探究患者对治疗药物的反应是个性化治疗研究中的关键且紧迫之事。利用机器学习方法发现适用性评估生物标志物能够深入洞察疾病治疗机制,并推动个性化医疗的发展。为了找到预测患者药物反应的重要代谢网络信号,提出了一种称为差异代谢网络构建(DMNC)的新方法。在DMNC中,测量不同病理状态之间代谢物比率的浓度变化以构建差异代谢网络,可用于推进临床决策。在本研究中,DMNC被应用于表征2型糖尿病(T2DM)患者对格列齐特缓释(MR)治疗的反应。对来自不同批次接受格列齐特MR治疗的受试者的两个T2DM代谢组学数据集进行了深入分析。定义了一个网络生物标志物来评估患者对格列齐特MR的适用性。它能有效区分显著反应者和非显著反应者,发现集和验证集的曲线下面积值分别达到0.893和1.000。与其他方法选择的代谢物相比,DMNC选择的网络生物标志物在反映患者对格列齐特MR治疗的代谢反应方面更稳定、精确,从而有助于T2DM患者的个性化医疗。DMNC的良好性能验证了其在识别网络生物标志物以表征对治疗的反应并为个性化医疗提供有价值信息方面的潜力。