多模态数据驱动的垂直可视化预测模型,用于早期预测新发高血压患者的动脉粥样硬化性心血管疾病。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2024-10-01 Epub Date: 2024-06-17 DOI:10.1097/HJH.0000000000003798
Jian Wang, Yanan Xu, Jiajun Zhu, Bing Wu, Yijun Wang, Liguo Tan, Long Tang, Jun Wang
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引用次数: 0

摘要

背景:高血压是动脉粥样硬化性心血管疾病(ASCVD)的重要诱因,而多种危险因素(其中许多与代谢紊乱有关)是导致高血压的原因。尽管多模态数据驱动预测模型前景广阔,但目前尚无此类预测模型用于预测中国新发高血压且无ASCVD病史者的ASCVD风险:方法:我们将 514 名患者随机分配到训练组和验证组(比例为 7:3)。我们采用 Boruta 特征选择法并进行多变量 Cox 回归分析,以确定这些患者中与 ASCVD 相关的变量,然后利用这些变量构建预测模型。从判别能力(C-指数)、校准(校准曲线)和临床实用性[决策曲线分析(DCA)]等方面对预测模型的性能进行了评估:该模型由四个临床变量得出:24 小时 SBP 变异系数、24 小时 DBP 变异系数、尿素氮和甘油三酯-葡萄糖(TyG)指数。对 C 指数进行了 500 次重复的 Bootstrapping 调整:C 指数 = 0.731,95% 置信区间(CI)0.620-0.794;C 指数 = 0.799,95% 置信区间(CI)0.620-0.794:训练组和验证组的 C 指数分别为 0.799,95% 置信区间为 0.677-0.892。500 次引导迭代的校准图显示,在训练队列和验证队列中,预测的 ASCVD 发生率与观察到的发生率之间存在很强的相关性。DCA分析证实了该预测模型的临床实用性。与整体 ASCVD 风险评估相比,所构建的提名图在 C 指数、净再分类改进、综合辨别改进和 DCA 方面均有改进,这证明所构建的提名图在 ASCVD 的预后方面具有显著的额外效用:结论:基于多模态数据开发的纵向预测模型可有效预测初诊高血压患者的 ASCVD 风险:该试验已在中国临床试验注册中心注册(ChiCTR2300074392)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multimodal data-driven, vertical visualization prediction model for early prediction of atherosclerotic cardiovascular disease in patients with new-onset hypertension.

Background: : Hypertension is an important contributing factor to atherosclerotic cardiovascular disease (ASCVD), and multiple risk factors, many of which are implicated in metabolic disorders, contribute to the cause of hypertension. Despite the promise of multimodal data-driven prediction model, no such prediction model was available to predict the risk of ASCVD in Chinese individuals with new-onset hypertension and no history of ASCVD.

Methods: : A total of 514 patients were randomly allocated to training and verification cohorts (ratio, 7 : 3). We employed Boruta feature selection and conducted multivariate Cox regression analyses to identify variables associated with ASCVD in these patients, which were subsequently utilized for constructing the predictive model. The performance of prediction model was assessed in terms of discriminatory power (C-index), calibration (calibration curves), and clinical utility [decision curve analysis (DCA)].

Results: : This model was derived from four clinical variables: 24-h SBP coefficient of variation, 24-h DBP coefficient of variation, urea nitrogen and the triglyceride-glucose (TyG) index. Bootstrapping with 500 iterations was conducted to adjust the C-indexes were C-index = 0.731, 95% confidence interval (CI) 0.620-0.794 and C-index: 0.799, 95% CI 0.677-0.892 in the training and verification cohorts, respectively. Calibration plots with 500 bootstrapping iterations exhibited a strong correlation between the predicted and observed occurrences of ASCVD in both the training and verification cohorts. DCA analysis confirmed the clinical utility of this prediction model. The constructed nomogram demonstrated significant additional prognostic utility for ASCVD, as evidenced by improvements in the C-index, net reclassification improvement, integrated discrimination improvement, and DCA compared with the overall ASCVD risk assessment.

Conclusion: The developed longitudinal prediction model based on multimodal data can effectively predict ASCVD risk in individuals with an initial diagnosis of hypertension.

Trial registration: : The trial was registered in the Chinese Clinical Trial Registry (ChiCTR2300074392).

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