Integrated-omics endotyping of infants with rhinovirus bronchiolitis and risk of childhood asthma

被引:46
作者
Raita, Yoshihiko [1 ]
Camargo, Carlos A., Jr. [1 ]
Bochkov, Yury A. [2 ]
Celedon, Juan C. [3 ]
Gern, James E. [2 ,4 ]
Mansbach, Jonathan M. [5 ]
Rhee, Eugene P. [6 ,7 ]
Freishtat, Robert J. [8 ,9 ,10 ]
Hasegawa, Kohei [1 ]
机构
[1] Harvard Med Sch, Dept Emergency Med, Massachusetts Gen Hosp, 125 Nashua St,Ste 920, Boston, MA 02114 USA
[2] Univ Wisconsin, Dept Pediat, Sch Med & Publ Hlth, Madison, WI USA
[3] Univ Pittsburgh, Dept Pediat, Div Pulm, UPMC Childrens Hosp Pittsburgh, Pittsburgh, PA 15260 USA
[4] Univ Wisconsin, Dept Med, Sch Med & Publ Hlth, Madison, WI USA
[5] Harvard Med Sch, Boston Childrens Hosp, Dept Pediat, Boston, MA 02115 USA
[6] Harvard Med Sch, Massachusetts Gen Hosp, Dept Med, Div Nephrol, Boston, MA 02115 USA
[7] Harvard Med Sch, Massachusetts Gen Hosp, Dept Med, Endocrine Unit, Boston, MA 02115 USA
[8] Childrens Natl Hosp, Div Emergency Med, Washington, DC USA
[9] George Washington Univ, Sch Med & Hlth Sci, Dept Pediat, Washington, DC 20052 USA
[10] George Washington Univ, Sch Med & Hlth Sci, Dept Genom & Precis Med, Washington, DC 20052 USA
基金
美国国家卫生研究院;
关键词
Integrated-omics; microbiome; metabolome; cytokines; endotyping; bronchiolitis; asthma; RESPIRATORY SYNCYTIAL VIRUS; DISEASE SEVERITY; MICROBIOTA; INFECTION; ASSOCIATION; PREVENTION; PROFILES; PATTERNS; CHILDREN; AIRWAY;
D O I
10.1016/j.jaci.2020.11.002
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Young children with rhinovirus (RV) infection-particularly bronchiolitis-are at high risk for developing childhood asthma. Emerging evidence suggests clinical heterogeneity within RV bronchiolitis. However, little is known about these biologically distinct subgroups (endotypes) and their relations with asthma risk. Objective: We aimed to identify RV bronchiolitis endotypes and examine their longitudinal relations with asthma risk. Methods: As part of a multicenter prospective cohort study of infants (age <12 months) hospitalized for bronchiolitis, we integrated clinical, RV species (RV-A, RV-B, and RV-C), nasopharyngeal microbiome (16S rRNA gene sequencing), cytokine, and metabolome (liquid chromatography tandem mass spectrometry) data collected at hospitalization. We then applied network and clustering approaches to identify bronchiolitis endotypes. We also examined their longitudinal association with risks of developing recurrent wheeze by age 3 years and asthma by age 5 years. Results: Of 122 infants hospitalized for RV bronchiolitis (median age, 4 months), we identified 4 distinct endotypes-mainly characterized by RV species, microbiome, and type 2 cytokine (T2) response: endotype A, virus(RV-C)microbiome(mixed) T2low; endotype B, virus(RV-A)microbiome(Haemophilus)T2(low); endotype C, virus(RSV/RV)microbiome(Streptococcus)T2(low); and endotype D, virus(RV-C)microbiome(Moraxella)T2(high). Compared with endotype A infants, endotype D infants had a significantly higher rate of recurrent wheeze (33% vs 64%; hazard ratio, 2.23; 95% CI, 1.00-4.96; P = .049) and a higher risk for developing asthma (28% vs 59%; odds ratio, 3.74: 95% CI, 1.21-12.6; P = .03). Conclusions: Integrated-omics analysis identified biologically meaningful RV bronchiolitis endotypes in infants, such as one characterized by RV-C infection, Moraxella-dominant microbiota, and high T2 cytokine response, at higher risk for developing recurrent wheeze and asthma. This study should facilitate further research toward validating our inferences.
引用
收藏
页码:2108 / 2117
页数:10
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