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急性冠状动脉综合征患者主要不良心血管事件的预测:基于自主神经系统评估的无创列线图模型的建立与验证

Prediction of major adverse cardiovascular events in patients with acute coronary syndrome: Development and validation of a non-invasive nomogram model based on autonomic nervous system assessment.

作者信息

Wang Jun, Wu Xiaolin, Sun Ji, Xu Tianyou, Zhu Tongjian, Yu Fu, Duan Shoupeng, Deng Qiang, Liu Zhihao, Guo Fuding, Li Xujun, Wang Yijun, Song Lingpeng, Feng Hui, Zhou Xiaoya, Jiang Hong

机构信息

Department of Cardiology, Renmin Hospital of Wuhan University, Wuhan, China.

Cardiac Autonomic Nervous System Research Center of Wuhan University, Wuhan, China.

出版信息

Front Cardiovasc Med. 2022 Nov 3;9:1053470. doi: 10.3389/fcvm.2022.1053470. eCollection 2022.

DOI:10.3389/fcvm.2022.1053470
PMID:36407419
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9670131/
Abstract

BACKGROUND

Disruption of the autonomic nervous system (ANS) can lead to acute coronary syndrome (ACS). We developed a nomogram model using heart rate variability (HRV) and other data to predict major adverse cardiovascular events (MACEs) following emergency coronary angiography in patients with ACS.

METHODS

ACS patients admitted from January 2018 to June 2020 were examined. Holter monitors were used to collect HRV data for 24 h. Coronary angiograms, clinical data, and MACEs were recorded. A nomogram was developed using the results of Cox regression analysis.

RESULTS

There were 439 patients in a development cohort and 241 in a validation cohort, and the mean follow-up time was 22.80 months. The nomogram considered low-frequency/high-frequency ratio, age, diabetes, previous myocardial infarction, and current smoking. The area-under-the-curve (AUC) values for 1-year MACE-free survival were 0.790 (95% CI: 0.702-0.877) in the development cohort and 0.894 (95% CI: 0.820-0.967) in the external validation cohort. The AUCs for 2-year MACE-free survival were 0.802 (95% CI: 0.739-0.866) in the development cohort and 0.798 (95% CI: 0.693-0.902) in the external validation cohort. Development and validation were adequately calibrated and their predictions correlated with the observed outcome. Decision curve analysis (DCA) showed the model had good discriminative ability in predicting MACEs.

CONCLUSION

Our validated nomogram was based on non-invasive ANS assessment and traditional risk factors, and indicated reliable prediction of MACEs in patients with ACS. This approach has potential for use as a method for non-invasive monitoring of health that enables provision of individualized treatment strategies.

摘要

背景

自主神经系统(ANS)紊乱可导致急性冠状动脉综合征(ACS)。我们利用心率变异性(HRV)和其他数据开发了一种列线图模型,以预测ACS患者急诊冠状动脉造影术后的主要不良心血管事件(MACE)。

方法

对2018年1月至2020年6月收治的ACS患者进行检查。使用动态心电图监测仪收集24小时的HRV数据。记录冠状动脉造影、临床数据和MACE。利用Cox回归分析结果开发列线图。

结果

开发队列中有439例患者,验证队列中有241例患者,平均随访时间为22.80个月。列线图考虑了低频/高频比值、年龄、糖尿病、既往心肌梗死和当前吸烟情况。开发队列中1年无MACE生存的曲线下面积(AUC)值为0.790(95%CI:0.702-0.877),外部验证队列中为0.894(95%CI:0.820-0.967)。开发队列中2年无MACE生存的AUC值为0.802(95%CI:0.739-0.866),外部验证队列中为0.798(95%CI:0.693-0.902)。开发和验证得到了充分校准,其预测与观察结果相关。决策曲线分析(DCA)表明该模型在预测MACE方面具有良好的判别能力。

结论

我们验证的列线图基于非侵入性ANS评估和传统危险因素,表明对ACS患者的MACE具有可靠的预测能力。这种方法有潜力用作一种非侵入性健康监测方法,能够提供个性化治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff39/9670131/926df1539a08/fcvm-09-1053470-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff39/9670131/af3031a72839/fcvm-09-1053470-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff39/9670131/0e8b2b96d18d/fcvm-09-1053470-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff39/9670131/60244e87e4c1/fcvm-09-1053470-g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff39/9670131/557b8079664c/fcvm-09-1053470-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff39/9670131/f109f6e7d775/fcvm-09-1053470-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff39/9670131/926df1539a08/fcvm-09-1053470-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff39/9670131/af3031a72839/fcvm-09-1053470-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff39/9670131/0e8b2b96d18d/fcvm-09-1053470-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff39/9670131/60244e87e4c1/fcvm-09-1053470-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff39/9670131/7da8cf8645d2/fcvm-09-1053470-g004.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff39/9670131/f109f6e7d775/fcvm-09-1053470-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff39/9670131/926df1539a08/fcvm-09-1053470-g007.jpg

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