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多组学生物标志物在食物过敏高危婴儿中的特征。

Multi-Omic Profiles in Infants at Risk for Food Reactions.

机构信息

Penn State Health Milton S Hershey Medical Center, Department of Pediatrics, Hershey, PA 17033, USA.

Department of Pediatrics, Penn State Health Children's Hospital, 500 University Drive, Hershey, PA 17033, USA.

出版信息

Genes (Basel). 2022 Nov 3;13(11):2024. doi: 10.3390/genes13112024.

Abstract

Food reactions (FR) are multifactorial and impacted by medical, demographic, environmental, and immunologic factors. We hypothesized that multi-omic analyses of host-microbial factors in saliva would enhance our understanding of FR development. This longitudinal cohort study included 164 infants followed from birth through two years. The infants were identified as FR ( = 34) or non-FR ( = 130) using the Infant Feeding Practice II survey and medical record confirmation. Saliva was collected at six months for the multi-omic assessment of cytokines, mRNAs, microRNAs, and the microbiome/virome. The levels of one miRNA (miR-203b-3p, adj. = 0.043, V = 2913) and one viral phage (Proteus virus PM135, adj. = 0.027, V = 2955) were lower among infants that developed FRs. The levels of one bacterial phylum (Cyanobacteria, adj. = 0.048, V = 1515) were higher among infants that developed FR. Logistical regression models revealed that the addition of multi-omic features (miR-203b-3p, Cyanobacteria, and Proteus virus PM135) improved predictiveness for future FRs in infants ( = 0.005, X = 12.9), predicting FRs with 72% accuracy (AUC = 0.81, sensitivity = 72%, specificity = 72%). The multi-omic analysis of saliva may enhance the accurate identification of infants at risk of FRs and provide insights into the host/microbiome interactions that predispose certain infants to FRs.

摘要

食物反应(FR)是多因素的,受医学、人口统计学、环境和免疫学因素的影响。我们假设,对唾液中宿主-微生物因素的多组学分析将增强我们对 FR 发展的理解。这项纵向队列研究包括 164 名婴儿,从出生到两岁进行随访。通过使用婴儿喂养实践 II 调查和医疗记录确认,将婴儿确定为 FR(=34)或非 FR(=130)。在六个月时收集唾液,以进行细胞因子、mRNA、microRNA 和微生物组/病毒组的多组学评估。在发生 FR 的婴儿中,有一种 miRNA(miR-203b-3p,adj. =0.043,V=2913)和一种病毒噬菌体(Proteus 病毒 PM135,adj. =0.027,V=2955)的水平较低。在发生 FR 的婴儿中,有一种细菌门(蓝细菌,adj. =0.048,V=1515)的水平较高。逻辑回归模型显示,多组学特征(miR-203b-3p、蓝细菌和 Proteus 病毒 PM135)的加入提高了对未来 FR 婴儿的预测能力(=0.005,X=12.9),预测 FR 的准确率为 72%(AUC=0.81,敏感性=72%,特异性=72%)。唾液的多组学分析可能增强对 FR 风险婴儿的准确识别,并深入了解使某些婴儿易患 FR 的宿主/微生物组相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8db/9690066/533bae99c10f/genes-13-02024-g001.jpg

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