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基于核支持向量回归的华法林抗凝药物调整初始治疗剂量的确定。

Determining the adjusted initial treatment dose of warfarin anticoagulant medicine using kernel-based support vector regression.

机构信息

Department of Computer Engineering, Science and Research Branch,Islamic Azad University, Tehran, Iran.

Department of Computer Engineering, Science and Research Branch,Islamic Azad University, Tehran, Iran.

出版信息

Comput Methods Programs Biomed. 2022 Feb;214:106589. doi: 10.1016/j.cmpb.2021.106589. Epub 2021 Dec 17.

DOI:10.1016/j.cmpb.2021.106589
PMID:34963093
Abstract

BACKGROUND AND OBJECTIVE

A novel research field in bioinformatics is pharmacogenomics and the corresponding applications of artificial intelligence tools. Pharmacogenomics is the study of the relationship between genotype and responses to medical measures such as drug use. One of the most effective drugs is warfarin anticoagulant, but determining its initial treatment dose is challenging. Mistakes in the determination of the initial treatment dose can result directly in patient death.

METHODS

Some of the most successful techniques for estimating the initial treatment dose are kernel-based methods. However, all the available studies use pre-defined and constant kernels that might not necessarily address the problem's intended requirements. The present study seeks to define and present a new computational kernel extracted from a data set. This process aims to utilize all the data-related statistical features to generate a dose determination tool proportional to the data set with minimum error rate. The kernel-based version of the least square support vector regression estimator was defined. Through this method, a more appropriate approach was proposed for predicting the adjusted dose of warfarin.

RESULTS AND CONCLUSION

This paper benefits from the International Warfarin Pharmacogenomics Consortium (IWPC) Database. The results obtained in this study demonstrate that the support vector regression with the proposed new kernel can successfully estimate the ideal dosage of warfarin for approximately 68% of patients.

摘要

背景与目的

生物信息学中的一个新研究领域是药物基因组学和人工智能工具的相应应用。药物基因组学是研究基因型与药物使用等医疗措施反应之间的关系。其中一种最有效的药物是华法林抗凝剂,但确定其初始治疗剂量具有挑战性。初始治疗剂量确定中的错误可能直接导致患者死亡。

方法

估计初始治疗剂量最成功的技术之一是基于核的方法。然而,所有现有的研究都使用预定义和恒定的核,这些核不一定能满足问题的预期要求。本研究旨在定义和提出一种从数据集提取的新计算核。该过程旨在利用所有与数据相关的统计特征,生成一个与数据集成比例的剂量确定工具,误差率最小。定义了基于核的最小二乘支持向量回归估计量的版本。通过这种方法,提出了一种更合适的方法来预测华法林的调整剂量。

结果与结论

本文受益于国际华法林药物基因组学联合会(IWPC)数据库。本研究的结果表明,带有所提出的新核的支持向量回归可以成功地估计约 68%患者的华法林理想剂量。

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