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川崎病患儿冠状动脉病变列线图的建立与验证

Establishment and validation of a nomogram for coronary artery lesions in children with Kawasaki disease.

作者信息

Hu Chong, Yan Xiao, Song Henglian, Dong Qin, Yi Changying, Li Jianzhi, Lv Xin

机构信息

Clinical Laboratory, Children's Hospital Affiliated to Shandong University, Jinan, China.

Clinical Laboratory, Jinan Children's Hospital, Jinan, China.

出版信息

Front Cardiovasc Med. 2025 Jan 14;11:1522473. doi: 10.3389/fcvm.2024.1522473. eCollection 2024.

DOI:10.3389/fcvm.2024.1522473
PMID:39877016
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11772273/
Abstract

BACKGROUND

The nomogram is a powerful and robust tool in disease risk prediction that summarizes complex variables into a visual model that is interpretable with a quantified risk probability. In the current study, a nomogram was developed to predict the occurrence of coronary artery lesions (CALs) among patients with Kawasaki disease (KD). This is especially valuable in the early identification of the risk of CALs, which will lead to proper diagnosis and treatment to reduce their associated complications.

METHODS

Retrospective clinical data of 677 children diagnosed with KD who were treated in the Children's Hospital Affiliated with Shandong University were analyzed. All the participants were divided into the CAL group and no CAL group according to their coronary echocardiography results. Least absolute shrinkage and selection operator (LASSO) regression was applied for the identification of the most informative predictors of CAL. Based on this, a nomogram was developed for accurate risk estimation.

RESULTS

The data were divided into a training set and a validation set. Receiver operating characteristic analysis, calibration curves, and decision curve analysis all supported the high accuracy and clinical utility of this model. LASSO regression highlighted five key predictors: sodium, hemoglobin, platelet count, D-dimer, and cystatin C. A nomogram based on these predictors was established and successfully validated in both datasets. In the training set, the AUC was 0.819 and in the validation set it was 0.844. The C-index of the calibration curve in the training set was 0.820, while in the validation set it was 0.844. In the decision curve analysis, the predictive benefit of the model was greater than zero when the threshold probability was below 95% in the training set and below 92% in the validation set.

CONCLUSION

The predictive factors identified through the LASSO regression approach and the development of the nomogram are important contributions in this respect. This model had a high predictive accuracy and reliability for identifying high-risk children in the very early stage of disease with remarkable precision, laying the foundation for personalized treatment strategies and targeted treatment and providing a strong scientific basis for precise therapeutic intervention.

摘要

背景

列线图是疾病风险预测中一种强大且可靠的工具,它将复杂变量汇总为一个可视模型,该模型可通过量化的风险概率进行解读。在本研究中,我们开发了一种列线图来预测川崎病(KD)患者冠状动脉病变(CALs)的发生情况。这对于早期识别CALs风险尤为重要,因为这将有助于进行正确的诊断和治疗,以减少相关并发症。

方法

分析了山东大学附属儿童医院收治的677例诊断为KD的儿童的回顾性临床数据。根据冠状动脉超声心动图结果,将所有参与者分为CAL组和无CAL组。应用最小绝对收缩和选择算子(LASSO)回归来确定CAL最具信息量的预测因子。在此基础上,开发了一种列线图用于准确的风险估计。

结果

数据分为训练集和验证集。受试者工作特征分析、校准曲线和决策曲线分析均支持该模型的高准确性和临床实用性。LASSO回归突出了五个关键预测因子:钠、血红蛋白、血小板计数、D-二聚体和胱抑素C。基于这些预测因子建立了列线图,并在两个数据集中均成功验证。在训练集中,AUC为0.819,在验证集中为0.844。训练集中校准曲线的C指数为0.820,而在验证集中为0.844。在决策曲线分析中,当阈值概率在训练集中低于95%且在验证集中低于92%时,模型的预测效益大于零。

结论

通过LASSO回归方法确定的预测因子以及列线图的开发在这方面具有重要意义。该模型在疾病极早期识别高危儿童方面具有很高的预测准确性和可靠性,为个性化治疗策略和靶向治疗奠定了基础,并为精确的治疗干预提供了有力的科学依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f372/11772273/6d6ef9b8e94f/fcvm-11-1522473-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f372/11772273/9fd3078d7706/fcvm-11-1522473-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f372/11772273/7050b6f7c08e/fcvm-11-1522473-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f372/11772273/93943c8b7e5b/fcvm-11-1522473-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f372/11772273/d390b1e9ae84/fcvm-11-1522473-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f372/11772273/9b6b326e27c6/fcvm-11-1522473-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f372/11772273/6d6ef9b8e94f/fcvm-11-1522473-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f372/11772273/9fd3078d7706/fcvm-11-1522473-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f372/11772273/7050b6f7c08e/fcvm-11-1522473-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f372/11772273/93943c8b7e5b/fcvm-11-1522473-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f372/11772273/d390b1e9ae84/fcvm-11-1522473-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f372/11772273/9b6b326e27c6/fcvm-11-1522473-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f372/11772273/6d6ef9b8e94f/fcvm-11-1522473-g006.jpg

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本文引用的文献

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Development of an immunoinflammatory indicator-related dynamic nomogram based on machine learning for the prediction of intravenous immunoglobulin-resistant Kawasaki disease patients.基于机器学习的免疫炎症指标相关动态列线图的建立及其对静脉注射免疫球蛋白抵抗川崎病的预测价值
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Exploring the diagnostic value of CLR and CPR in differentiating Kawasaki disease from other infectious diseases based on clinical predictive modeling.基于临床预测模型探索CLR和CPR在鉴别川崎病与其他传染病中的诊断价值。
Front Pediatr. 2024 Feb 16;12:1345141. doi: 10.3389/fped.2024.1345141. eCollection 2024.
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The etiologies of Kawasaki disease.
川崎病的病因。
J Clin Invest. 2024 Mar 1;134(5):e176938. doi: 10.1172/JCI176938.
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Prediction nomogram for coronary artery aneurysms at one month in Kawasaki disease.川崎病患者冠状动脉瘤 1 个月的预测列线图。
Ital J Pediatr. 2023 Nov 6;49(1):146. doi: 10.1186/s13052-023-01551-3.
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Diagnosis, Progress, and Treatment Update of Kawasaki Disease.川崎病的诊断、进展和治疗更新。
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Nomogram for predicting coronary artery lesions in patients with Kawasaki disease.预测川崎病患者冠状动脉病变的列线图。
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Platelets promote cardiovascular complications in Kawasaki disease.血小板会引发川崎病的心血管并发症。
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Bioinformatic analysis of underlying mechanisms of Kawasaki disease via Weighted Gene Correlation Network Analysis (WGCNA) and the Least Absolute Shrinkage and Selection Operator method (LASSO) regression model.通过加权基因共表达网络分析(WGCNA)和最小绝对收缩与选择算子法(LASSO)回归模型对川崎病潜在机制的生物信息学分析
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