囊性纤维化儿童新发铜绿假单胞菌肺部感染抗生素根除治疗成功的预测模型。

IF 4.3 2区 生物学 PLoS Computational Biology Pub Date : 2023-09-06 eCollection Date: 2023-09-01 DOI:10.1371/journal.pcbi.1011424
Lucía Graña-Miraglia, Nadia Morales-Lizcano, Pauline W Wang, David M Hwang, Yvonne C W Yau, Valerie J Waters, David S Guttman
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引用次数: 0

摘要

慢性铜绿假单胞菌(Pa)肺部感染是囊性纤维化(CF)患者死亡的主要原因;因此,根除新发Pa肺部感染是一个重要的治疗目标,可以对健康产生长期益处。早期抗生素根除治疗(AET)的使用已被证明可以清除大多数新发Pa感染,希望确定AET失败的潜在基础将进一步改善治疗结果。在这里,我们生成了基于病原体基因组数据预测AET结果的机器学习模型。我们使用嵌套交叉验证设计、总体结构控制和递归特征选择来提高模型性能,并表明结合总体结构控制对于提高模型解释和可推广性至关重要。我们的最佳模型控制了种群结构,只使用了30个递归选择的特征,对于一个拒绝测试数据集,其曲线下面积为0.87。排名靠前的特征通常与运动性、粘附性和生物膜形成有关。
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Predictive modeling of antibiotic eradication therapy success for new-onset Pseudomonas aeruginosa pulmonary infections in children with cystic fibrosis.

Chronic Pseudomonas aeruginosa (Pa) lung infections are the leading cause of mortality among cystic fibrosis (CF) patients; therefore, the eradication of new-onset Pa lung infections is an important therapeutic goal that can have long-term health benefits. The use of early antibiotic eradication therapy (AET) has been shown to clear the majority of new-onset Pa infections, and it is hoped that identifying the underlying basis for AET failure will further improve treatment outcomes. Here we generated machine learning models to predict AET outcomes based on pathogen genomic data. We used a nested cross validation design, population structure control, and recursive feature selection to improve model performance and showed that incorporating population structure control was crucial for improving model interpretation and generalizability. Our best model, controlling for population structure and using only 30 recursively selected features, had an area under the curve of 0.87 for a holdout test dataset. The top-ranked features were generally associated with motility, adhesion, and biofilm formation.

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PLoS Computational Biology
PLoS Computational Biology 生物-生化研究方法
CiteScore
7.10
自引率
4.70%
发文量
820
期刊介绍: PLOS Computational Biology features works of exceptional significance that further our understanding of living systems at all scales—from molecules and cells, to patient populations and ecosystems—through the application of computational methods. Readers include life and computational scientists, who can take the important findings presented here to the next level of discovery. Research articles must be declared as belonging to a relevant section. More information about the sections can be found in the submission guidelines. Research articles should model aspects of biological systems, demonstrate both methodological and scientific novelty, and provide profound new biological insights. Generally, reliability and significance of biological discovery through computation should be validated and enriched by experimental studies. Inclusion of experimental validation is not required for publication, but should be referenced where possible. Inclusion of experimental validation of a modest biological discovery through computation does not render a manuscript suitable for PLOS Computational Biology. Research articles specifically designated as Methods papers should describe outstanding methods of exceptional importance that have been shown, or have the promise to provide new biological insights. The method must already be widely adopted, or have the promise of wide adoption by a broad community of users. Enhancements to existing published methods will only be considered if those enhancements bring exceptional new capabilities.
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