Suppr超能文献

用于预测美国拉丁裔和拉丁美洲人华法林稳定剂量的机器学习

Machine Learning for Prediction of Stable Warfarin Dose in US Latinos and Latin Americans.

作者信息

Steiner Heidi E, Giles Jason B, Patterson Hayley Knight, Feng Jianglin, El Rouby Nihal, Claudio Karla, Marcatto Leiliane Rodrigues, Tavares Leticia Camargo, Galvez Jubby Marcela, Calderon-Ospina Carlos-Alberto, Sun Xiaoxiao, Hutz Mara H, Scott Stuart A, Cavallari Larisa H, Fonseca-Mendoza Dora Janeth, Duconge Jorge, Botton Mariana Rodrigues, Santos Paulo Caleb Junior Lima, Karnes Jason H

机构信息

Department of Pharmacy Practice and Science, University of Arizona College of Pharmacy, Tucson, AZ, United States.

Department of Pharmacotherapy and Translational Research and Center for Pharmacogenomics and Precision Medicine, University of Florida College of Pharmacy, Gainesville, FL, United States.

出版信息

Front Pharmacol. 2021 Oct 29;12:749786. doi: 10.3389/fphar.2021.749786. eCollection 2021.

Abstract

Populations used to create warfarin dose prediction algorithms largely lacked participants reporting Hispanic or Latino ethnicity. While previous research suggests nonlinear modeling improves warfarin dose prediction, this research has mainly focused on populations with primarily European ancestry. We compare the accuracy of stable warfarin dose prediction using linear and nonlinear machine learning models in a large cohort enriched for US Latinos and Latin Americans (ULLA). Each model was tested using the same variables as published by the International Warfarin Pharmacogenetics Consortium (IWPC) and using an expanded set of variables including ethnicity and warfarin indication. We utilized a multiple linear regression model and three nonlinear regression models: Bayesian Additive Regression Trees, Multivariate Adaptive Regression Splines, and Support Vector Regression. We compared each model's ability to predict stable warfarin dose within 20% of actual stable dose, confirming trained models in a 30% testing dataset with 100 rounds of resampling. In all patients ( = 7,030), inclusion of additional predictor variables led to a small but significant improvement in prediction of dose relative to the IWPC algorithm (47.8 versus 46.7% in IWPC, = 1.43 × 10). Nonlinear models using IWPC variables did not significantly improve prediction of dose over the linear IWPC algorithm. In ULLA patients alone ( = 1,734), IWPC performed similarly to all other linear and nonlinear pharmacogenetic algorithms. Our results reinforce the validity of IWPC in a large, ethnically diverse population and suggest that additional variables that capture warfarin dose variability may improve warfarin dose prediction algorithms.

摘要

用于创建华法林剂量预测算法的人群在很大程度上缺乏报告西班牙裔或拉丁裔种族的参与者。虽然先前的研究表明非线性建模可改善华法林剂量预测,但这项研究主要集中在主要具有欧洲血统的人群上。我们比较了在一个富含美国拉丁裔和拉丁美洲人(ULLA)的大型队列中使用线性和非线性机器学习模型进行稳定华法林剂量预测的准确性。每个模型都使用与国际华法林药物遗传学联盟(IWPC)公布的相同变量进行测试,并使用包括种族和华法林适应症在内的一组扩展变量进行测试。我们使用了多元线性回归模型和三种非线性回归模型:贝叶斯加法回归树、多元自适应回归样条和支持向量回归。我们比较了每个模型在实际稳定剂量的20%范围内预测稳定华法林剂量的能力,在一个30%的测试数据集中通过100轮重采样对训练模型进行了验证。在所有患者(n = 7,030)中,相对于IWPC算法,纳入额外的预测变量导致剂量预测有小幅但显著的改善(IWPC为46.7%,纳入额外变量后为47.8%,p = 1.43×10⁻⁴)。使用IWPC变量的非线性模型在剂量预测方面并未比线性IWPC算法有显著改善。仅在ULLA患者(n = 1,734)中,IWPC的表现与所有其他线性和非线性药物遗传学算法相似。我们的结果强化了IWPC在一个大型、种族多样化人群中的有效性,并表明捕获华法林剂量变异性的额外变量可能会改善华法林剂量预测算法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6265/8585774/6c10c538df2b/fphar-12-749786-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验