Serum Soluble Receptor for Advanced Glycation End Products in Infants With Bronchiolitis: Associations With Acute Severity and Recurrent Wheeze

Author:

Patregnani Jason T1234ORCID,Fujiogi Michimasa5,Camargo Carlos A5,Brooks Bonnie A1,Hoptay Claire E2,Mansbach Jonathan M6,Teach Stephen J7,Freishtat Robert J27,Hasegawa Kohei5

Affiliation:

1. Division of Cardiac Critical Care Medicine, Children’s National Hospital, Washington, DC, USA

2. Department of Genomics and Precision Medicine, George Washington University, Washington, DC, USA

3. Division of Pediatric Critical Care Medicine, Maine Medical Center, Portland, Maine, USA

4. Tufts University, Medford, Massachusetts, USA

5. Department of Emergency Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA

6. Division of General Pediatrics, Boston Children’s Hospital, Harvard Medical School, Boston, Massachusetts, USA

7. Division of Emergency Medicine, Children’s National Hospital, Washington, DC, USA

Abstract

Abstract Background Although bronchiolitis contributes to substantial acute (eg, intensive care use) and chronic (eg, recurrent wheeze) morbidities in young children, the pathobiology remains uncertain. We examined the associations of serum soluble receptor for advanced glycation end products (sRAGE) with acute and chronic morbidities of bronchiolitis including recurrent wheeze. Methods A multicenter, multiyear, cohort study of infants hospitalized for bronchiolitis was analyzed. We measured the serum sRAGE level at hospitalization and its association with intensive care use (use of mechanical ventilation and/or admission to the intensive care unit) and development of recurrent wheeze by age 3 years. We performed causal mediation analysis to estimate indirect (mediation) and direct effects of sRAGE on recurrent wheeze. Results In 886 infants with bronchiolitis, the median age was 2.9 months. Overall, 15% underwent intensive care and 32% developed recurrent wheeze. In multivariable modeling adjusting for 11 confounders, a higher presenting sRAGE level was associated with lower risk of intensive care (odds ratio for each 1-log increment, 0.39; 95% confidence interval [CI], .16 -.91; P = .03) and significantly lower rate of recurrent wheeze (hazard ratio [HR], 0.58; 95% CI, .36 -.94; P = .03). In mediation analysis, the direct effect was significant (HR, 0.60; 95% CI, .37 -.97; P = .04), while the indirect effect was not (P = .30). Conclusions Serum sRAGE levels were inversely associated with acute and chronic morbidities of bronchiolitis. The effect of sRAGE on development of recurrent wheeze is potentially driven through pathways other than acute severity of bronchiolitis.

Funder

NIH

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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