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Fetal lung growth predicts the risk for early-life respiratory infections and childhood asthma

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摘要 Background Early-life respiratory infections and asthma are major health burdens during childhood.Markers predicting an increased risk for early-life respiratory diseases are sparse.Here,we identified the predictive value of ultrasound-monitored fetal lung growth for the risk of early-life respiratory infections and asthma.Methods Fetal lung size was serially assessed at standardized time points by transabdominal ultrasound in pregnant women participating in a pregnancy cohort.Correlations between fetal lung growth and respiratory infections in infancy or early-onset asthma at five years were examined.Machine-learning models relying on extreme gradient boosting regressor or classifier algorithms were developed to predict respiratory infection or asthma risk based on fetal lung growth.For model development and validation,study participants were randomly divided into a training and a testing group,respectively,by the employed algorithm.Results Enhanced fetal lung growth throughout pregnancy predicted a lower early-life respiratory infection risk.Male sex was associated with a higher risk for respiratory infections in infancy.Fetal lung growth could also predict the risk of asthma at five years of age.We designed three machine-learning models to predict the risk and number of infections in infancy as well as the risk of early-onset asthma.The models’R2 values were 0.92,0.90 and 0.93,respectively,underscoring a high accuracy and agreement between the actual and predicted values.Influential variables included known risk factors and novel predictors,such as ultrasound-monitored fetal lung growth.Conclusion Sonographic monitoring of fetal lung growth allows to predict the risk for early-life respiratory infections and asthma.
出处 《World Journal of Pediatrics》 SCIE CSCD 2024年第5期481-495,共15页 世界儿科杂志(英文版)
基金 supported by the German Research Foundation to ZDE,APC and DA(CRU296:AR232/25-2,DI 2103/2-1,SO1413/1-2,ZA1246/2-1,FOR5068:AR232/29-1) the Authority for Science,Research and Equality,Hanseatic City of Hamburg,Germany to APC and DA(LFF-FV73) the Werner Otto Foundation to ZDE and GAD ZDE and GAD are supported by the Clinician Scientist program of the RU5068 the Medical Faculty of the University of Hamburg.
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