预测冠状动脉钙化和严重冠状动脉钙化的提名图的开发与验证:一项回顾性横断面研究

Peng Xue, Ling Lin, Peishan Li, Zhengting Deng, Xiaohu Chen, Yanshuang Zhuang
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引用次数: 0

摘要

背景:目前严重缺乏治疗冠状动脉钙化(CAC)的有效药物干预措施。严重的冠状动脉钙化(sCAC)对介入手术提出了严峻的挑战,并与不良心血管预后密切相关。因此,当务之急是开发能够对 CAC 和 sCAC 进行早期检测和风险评估的工具。本研究旨在开发和验证用于准确预测 CAC 和 sCAC 的提名图。方法:这项回顾性横断面研究在中国江苏省泰州市进行。使用非门控胸部 CT 扫描进行 CAC 评估。研究人员收集了患者的人口统计学数据和临床信息,然后将患者随机分为训练集(70%)和验证集(30%)。利用最小绝对收缩和选择算子(LASSO)回归和多元逻辑回归分析来确定 CAC 和 sCAC 发展的预测因素。开发了预测 CAC 或 sCAC 事件发生的命定图。通过辨别分析、校准分析以及临床实用性评估,对模型的性能进行了评估。结果:这项研究包括 666 名平均年龄为 75 岁的患者,其中 56% 为男性。391 名患者患有 CAC,其中 134 例为 sCAC。通过 LASSO 和多元逻辑回归分析,确定了 CAC 风险预测提名图的年龄增长、高血压、颈动脉钙化、CHD 和 CHADS2 评分,训练集的接收器操作特征曲线下面积 (ROC) 为 0.845(95%CI 0.809-0.881),验证集的接收器操作特征曲线下面积 (AUC) 为 0.810(95%CI 0.751-0.870)。血清钙水平、颈动脉钙化和 CHD 被确定为 sCAC 风险预测提名图,训练集的 AUC 为 0.863(95%CI 0.825-0.901),验证集的 AUC 为 0.817(95%CI 0.744-0.890)。校准图显示,两个模型具有良好的校准能力。根据决策曲线分析(DCA)结果,两个模型都在广泛的风险范围内显示了正净效益。结论:本研究成功开发并验证了两个可准确预测 CAC 和 sCAC 的提名图,这两个提名图均表现出强大的预测能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development and Validation of Nomograms for predicting Coronary Artery Calcification and Severe Coronary Artery Calcification: a retrospective cross-sectional study
Background: There is a significant lack of effective pharmaceutical interventions for treating coronary artery calcification (CAC). Severe CAC (sCAC) poses a formidable challenge to interventional surgery and exhibits robust associations with adverse cardiovascular outcomes. Therefore, it is imperative to develop tools capable of early-stage detection and risk assessment for both CAC and sCAC. This study aims to develop and validate nomograms for the accurate prediction of CAC and sCAC. Methods: This retrospective cross-sectional study was conducted in Taizhou, Jiangsu Province, China. CAC assessment was performed using non-gated thoracic CT scans. Demographic data and clinical information were collected from patients who were then randomly divided into a training set (70%) or a validation set (30%). Least absolute shrinkage and selection operator (LASSO) regression as well as multiple logistic regression analyses were utilized to identify predictive factors for both CAC and sCAC development. Nomograms were developed to predict the occurrence of CAC or sCAC events. The models' performance was evaluated through discrimination analysis, calibration analysis, as well as assessment of their clinical utility. Results: This study included 666 patients with an average age of 75 years, of whom 56% were male. 391 patients had CAC, with sCAC in 134 cases. Through LASSO and multiple logistic regression analysis, age increase, hypertension, carotid artery calcification, CHD, and CHADS2 score were identified for the CAC risk predictive nomogram with an area under the receiver operating characteristic (ROC) curve (AUC) of 0.845(95%CI 0.809-0.881) in the training set and 0.810(95%CI 0.751-0.870) in the validation set. Serum calcium level, carotid artery calcification, and CHD were identified for the sCAC risk predictive nomogram with an AUC of 0.863(95%CI 0.825-0.901) in the training set and 0.817(95%CI 0.744-0.890) in the validation set. Calibration plots indicated that two models exhibited good calibration ability. According to the decision curve analysis (DCA) results, both models have demonstrated a positive net benefit within a wide range of risks. Conclusions: The present study has successfully developed and validated two nomograms to accurately predict CAC and sCAC, both of which have demonstrated robust predictive capabilities.
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