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孕龄小于32周早产儿短期神经发育障碍的预测模型

A prediction model for short-term neurodevelopmental impairment in preterm infants with gestational age less than 32 weeks.

作者信息

Li Yan, Zhang Zhihui, Mo Yan, Wei Qiufen, Jing Lianfang, Li Wei, Luo Mengmeng, Zou Linxia, Liu Xin, Meng Danhua, Shi Yuan

机构信息

Department of Neonatology, Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatrics, Chongqing, China.

Department of Applied Mathematics, The Hong Kong Polytechnic University, Kowloon, Hong Kong SAR, China.

出版信息

Front Neurosci. 2023 Apr 24;17:1166800. doi: 10.3389/fnins.2023.1166800. eCollection 2023.

DOI:10.3389/fnins.2023.1166800
PMID:37168928
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10166208/
Abstract

INTRODUCTION

Early identification and intervention of neurodevelopmental impairment in preterm infants may significantly improve their outcomes. This study aimed to build a prediction model for short-term neurodevelopmental impairment in preterm infants using machine learning method.

METHODS

Preterm infants with gestational age  < 32 weeks who were hospitalized in The Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, and were followed-up to 18 months corrected age were included to build the prediction model. The training set and test set are divided according to 8:2 randomly by Microsoft Excel. We firstly established a logistic regression model to screen out the indicators that have a significant effect on predicting neurodevelopmental impairment. The normalized weights of each indicator were obtained by building a Support Vector Machine, in order to measure the importance of each predictor, then the dimension of the indicators was further reduced by principal component analysis methods. Both discrimination and calibration were assessed with a bootstrap of 505 resamples.

RESULTS

In total, 387 eligible cases were collected, 78 were randomly selected for external validation. Multivariate logistic regression demonstrated that gestational age( = 0.0004), extrauterine growth restriction ( = 0.0367), vaginal delivery ( = 0.0009), and hyperbilirubinemia (0.0015) were more important to predict the occurrence of neurodevelopmental impairment in preterm infants. The Support Vector Machine had an area under the curve of 0.9800 on the training set. The results of the model were exported based on 10-fold cross-validation. In addition, the area under the curve on the test set is 0.70. The external validation proves the reliability of the prediction model.

CONCLUSION

A support vector machine based on perinatal factors was developed to predict the occurrence of neurodevelopmental impairment in preterm infants with gestational age  < 32 weeks. The prediction model provides clinicians with an accurate and effective tool for the prevention and early intervention of neurodevelopmental impairment in this population.

摘要

引言

早产儿神经发育障碍的早期识别和干预可能会显著改善其预后。本研究旨在使用机器学习方法建立早产儿短期神经发育障碍的预测模型。

方法

纳入在广西壮族自治区妇幼保健院住院的孕周<32周且随访至矫正年龄18个月的早产儿,以建立预测模型。通过Microsoft Excel按8:2随机划分训练集和测试集。我们首先建立逻辑回归模型以筛选出对预测神经发育障碍有显著影响的指标。通过构建支持向量机获得各指标的标准化权重,以衡量每个预测因子的重要性,然后用主成分分析方法进一步降低指标维度。通过505次重采样的自助法评估区分度和校准度。

结果

共收集387例符合条件的病例,随机选取78例进行外部验证。多因素逻辑回归显示,孕周(=0.0004)、宫外生长受限(=0.0367)、阴道分娩(=0.0009)和高胆红素血症(0.0015)对预测早产儿神经发育障碍的发生更为重要。支持向量机在训练集上的曲线下面积为0.9800。基于10倍交叉验证导出模型结果。此外,测试集上的曲线下面积为0.70。外部验证证明了预测模型的可靠性。

结论

建立了基于围产期因素的支持向量机,以预测孕周<32周的早产儿神经发育障碍的发生。该预测模型为临床医生提供了一种准确有效的工具,用于该人群神经发育障碍的预防和早期干预。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b62/10166208/c9593020bbfe/fnins-17-1166800-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b62/10166208/f285f40913e4/fnins-17-1166800-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b62/10166208/2dbfc9f9bccb/fnins-17-1166800-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b62/10166208/5d2f39f31815/fnins-17-1166800-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b62/10166208/0eecba195e14/fnins-17-1166800-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b62/10166208/c9593020bbfe/fnins-17-1166800-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b62/10166208/f285f40913e4/fnins-17-1166800-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b62/10166208/2dbfc9f9bccb/fnins-17-1166800-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b62/10166208/5d2f39f31815/fnins-17-1166800-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b62/10166208/0eecba195e14/fnins-17-1166800-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b62/10166208/c9593020bbfe/fnins-17-1166800-g005.jpg

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