使用决策树的代谢综合征预测和分类途径的发展和验证

Brian Miller, M. Fridline
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引用次数: 8

摘要

目的:当前研究的目的是创建、比较和验证性别特异性决策树模型,以对代谢综合征进行分类。方法:使用代谢综合征分类标准、受试者特征和来自全国健康与营养检查队列数据的心血管预测变量,对性别特异性卡方自动交互检测、穷举式卡方自动交互检测以及分类和回归树算法进行重复运行。使用1999-2012年的数据(n=10,639;1999-2010年的队列用于模型创建,2011-2012年的队列用于模型验证)。代谢综合征被归类为存在美国心脏协会国家心肺血液研究所代谢综合征分类标准中的3个。第一次运行使用所有预测变量,第二次运行排除代谢综合征分类预测变量。考虑到所包含的决策树算法是非参数过程,将所有决策树模型与基于逻辑回归的模型进行比较,以提供参数比较。结果:分类回归树算法的特异性分别为0.908和0.952,敏感性分别为0.896和0.848,男性和女性的误分类误差分别为0.096和0.080,优于其他决策树模型和逻辑回归。在女性模型中,除了代谢综合征分类外,只有一个预测变量(年龄)具有显著性。所有代谢综合征分类预测变量在男性模型中均达到显著性。女性模特的腰围没有达到显著性。在每个模型中,根据<3美国心脏协会国家心肺和血液研究所代谢综合征分类标准建立的5个女性和3个男性途径导致出现代谢综合征的可能性增加。结论:在目前的分类标准之前,所提出的途径在识别具有<3个预测变量的代谢综合征方面比其他现有的代谢综合征分类模型更有希望。
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Development and Validation of Metabolic Syndrome Prediction and Classification-Pathways using Decision Trees
Purpose: The purpose of the current investigation was to create, compare, and validate sex-specific decision tree models to classify metabolic syndrome. Methods: Sex-specific Chi-Squared Automatic Interaction Detection, Exhaustive Chi-Squared Automatic Interaction Detection, and Classification and Regression Tree algorithms were run in duplicate using metabolic syndrome classification criteria, subject characteristics, and cardiovascular predictor variable from the National Health and Nutrition Examination Survey cohort data. Data from 1999-2012 were used (n=10,639; 1999-2010 cohorts for model creation and 2011-2012 cohort for model validation). Metabolic Syndrome was classified as the presence of 3 of 5 American Heart Association National Heart Lung and Blood Institute Metabolic Syndrome classification criteria. The first run was made with all predictor variables and the second run was made excluding metabolic syndrome classification predictor variables. Given that the included decision tree algorithms are non-parametric procedures, all decision tree models were compared to a logistic regression based model to provide a parametric comparison. Results: The Classification and Regression Tree algorithm outperformed all other decision tree models and logistic regression with a specificity of 0.908 and 0.952, sensitivity of 0.896 and 0.848, and misclassification error of 0.096 and 0.080 for males and females, respectively. Only one predictor variable outside of the metabolic syndrome classification reached significance in the female model (age). All metabolic syndrome classification predictor variables reached significance in the male model. Waist circumference did not reach significance in the female model. Within each model, 5 female and 3 male pathways built off of <3 American Heart Association National Heart Lung and Blood Institute Metabolic Syndrome classification criteria resulted in an increased likelihood of presenting Metabolic Syndrome. Conclusion: The proposed pathways show promise over other current metabolic syndrome classification models in identifying Metabolic Syndrome with <3 predictor variables, before current classification criteria.
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