Galván-Tejada Carlos E, Villagrana-Bañuelos Karen E, Zanella-Calzada Laura A, Moreno-Báez Arturo, Luna-García Huizilopoztli, Celaya-Padilla Jose M, Galván-Tejada Jorge I, Gamboa-Rosales Hamurabi
Unidad Académica de Ingeniería Eléctrica, Universidad Autónoma de Zacatecas, Jardín Juarez 147, Centro, Zacatecas 98000, Mexico.
LORIA (INRIA, CNRS), Campus Scientifique BP 239, Université de Lorraine, 54506 Nancy, France.
Diagnostics (Basel). 2020 Nov 2;10(11):896. doi: 10.3390/diagnostics10110896.
Sudden infant death syndrome (SIDS) is defined as the death of a child under one year of age, during sleep, without apparent cause, after exhaustive investigation, so it is a diagnosis of exclusion. SIDS is the principal cause of death in industrialized countries. Inborn errors of metabolism (IEM) have been related to SIDS. These errors are a group of conditions characterized by the accumulation of toxic substances usually produced by an enzyme defect and there are thousands of them and included are the disorders of the β-oxidation cycle, similarly to what can affect the metabolism of different types of fatty acid chain (within these, short chain fatty acids (SCFAs)). In this work, an analysis of postmortem SCFAs profiles of children who died due to SIDS is proposed. Initially, a set of features containing SCFAs information, obtained from the NIH Common Fund's National Metabolomics Data Repository (NMDR) is submitted to an univariate analysis, developing a model based on the relationship between each feature and the binary output (death due to SIDS or not), obtaining 11 univariate models. Then, each model is validated, calculating their receiver operating characteristic curve (ROC curve) and area under the ROC curve (AUC) value. For those features whose models presented an AUC value higher than 0.650, a new multivariate model is constructed, in order to validate its behavior in comparison to the univariate models. In addition, a comparison between this multivariate model and a model developed based on the whole set of features is finally performed. From the results, it can be observed that each SCFA which comprises of the SFCAs profile, has a relationship with SIDS and could help in risk identification.
婴儿猝死综合征(SIDS)被定义为一岁以下儿童在睡眠中无明显原因死亡,经过详尽调查后确诊,因此它是一种排除性诊断。SIDS是工业化国家儿童死亡的主要原因。先天性代谢缺陷(IEM)与SIDS有关。这些缺陷是一组以通常由酶缺陷产生的有毒物质积累为特征的病症,有数千种之多,包括β-氧化循环紊乱,类似于影响不同类型脂肪酸链(其中包括短链脂肪酸(SCFA))代谢的情况。在这项工作中,提出了对因SIDS死亡儿童的死后SCFA谱进行分析。首先,将从美国国立卫生研究院共同基金的国家代谢组学数据存储库(NMDR)获得的一组包含SCFA信息的特征提交给单变量分析,基于每个特征与二元输出(是否死于SIDS)之间的关系建立模型,得到11个单变量模型。然后,对每个模型进行验证,计算其受试者工作特征曲线(ROC曲线)和ROC曲线下面积(AUC)值。对于那些模型的AUC值高于0.650的特征,构建一个新的多变量模型,以验证其与单变量模型相比的性能。此外,最终将这个多变量模型与基于整个特征集开发的模型进行比较。从结果可以看出,构成SCFA谱的每种SCFA都与SIDS有关系,并且有助于风险识别。