Phenotypical Sub-setting of the First Episode of Severe Viral Respiratory Infection Based on Clinical Assessment and Underlying Airway Disease: A Pilot Study

被引:17
作者
Arroyo, Maria [1 ]
Salka, Kyle [1 ]
Perez, Geovanny F. [1 ]
Rodriguez-Martinez, Carlos E. [2 ,3 ]
Castro-Rodriguez, Jose A. [4 ]
Gutierrez, Maria J. [5 ]
Nino, Gustavo [1 ]
机构
[1] George Washington Univ, Childrens Natl Med Ctr, Div Pediat Pulm & Sleep Med, Ctr Genet Res, Washington, DC 20052 USA
[2] Univ Nacl Colombia, Sch Med, Dept Pediat, Bogota, Colombia
[3] Univ El Bosque, Sch Med, Dept Pediat Pulmonol & Pediat Crit Care Med, Bogota, Colombia
[4] Pontificia Univ Catolica Chile, Sch Med, Dept Pediat Pulmonol, Div Pediat, Santiago, Chile
[5] Johns Hopkins Univ, Div Pediat Allergy & Immunol, Baltimore, MD USA
来源
FRONTIERS IN PEDIATRICS | 2020年 / 8卷
关键词
wheezing; cytokines; respiratory viral; airway immunity; viral bronchiolitis phenotyping; BRONCHIOLITIS; CHILDREN; MULTICENTER; DEFINITION; ETIOLOGY;
D O I
10.3389/fped.2020.00121
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Introduction: Viral bronchiolitis is a term often used to group all infants with the first episode of severe viral respiratory infection. However, this term encompasses a collection of different clinical and biological processes. We hypothesized that the first episode of severe viral respiratory infection in infants can be subset into clinical phenotypes with distinct outcomes and underlying airway disease patterns. Methods: We included children (<= 2 years old) hospitalized for the first time due to PCR-confirmed viral respiratory infection. All cases were categorized based on primary manifestations (wheezing, sub-costal retractions and hypoxemia) into mild, hypoxemia or wheezing phenotypes. We characterized these phenotypes using lung-X-rays, respiratory outcomes and nasal protein levels of antiviral and type 2 cytokines (IFN gamma, IL-10, IL-4, IL-13, IL-1 beta, and TNF alpha). Results: A total of 50 young children comprising viral respiratory infection cases (n = 41) and uninfected controls (n = 9) were included. We found that 22% of viral respiratory infection cases were classified as mild (n = 9), 39% as hypoxemia phenotype (n = 16) and 39% as wheezing phenotype (n = 16). Individuals in the hypoxemia phenotype had more lung opacities, higher probability of PICU admission and prolonged hospitalizations. Subjects in the wheezing phenotype had higher probability of recurrent sick visits. Nasal cytokine profiles showed that individuals with recurrent sick visits in the wheezing phenotype had increased nasal airway levels of type 2 cytokines (IL-13/IL-4). Conclusion: Clinically-based classification of the first episode of severe viral respiratory infection into mild, hypoxemia or wheezing phenotypes provides critical information about respiratory outcomes, lung disease patterns and underlying airway immunobiology.
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页数:7
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