Sphingolipid classes and the interrelationship with pediatric asthma and asthma risk factors

Author:

Chen Yulu1ORCID,Checa Antonio23,Zhang Pei24,Huang Mengna1,Kelly Rachel S.1ORCID,Kim Min5ORCID,Chen Yih‐Chieh S.16,Lee‐Sarwar Kathleen A.16,Prince Nicole1,Mendez Kevin M.1,Begum Sofina1,Kachroo Priyadarshini1,Chu Su H.1,Stokholm Jakob5ORCID,Bønnelykke Klaus5,Litonjua Augusto A.7,Bisgaard Hans5ORCID,Weiss Scott T.1,Chawes Bo L.5ORCID,Wheelock Craig E.234,Lasky‐Su Jessica A.1

Affiliation:

1. Channing Division of Network Medicine, Department of Medicine Brigham and Women's Hospital and Harvard Medical School Boston Massachusetts USA

2. Unit of Integrative Metabolomics, Institute of Environmental Medicine Karolinska Institute Stockholm Sweden

3. Department of Respiratory Medicine and Allergy Karolinska University Hospital Stockholm Sweden

4. Gunma University Initiative for Advanced Research (GIAR) Gunma University Maebashi Gunma Japan

5. Copenhagen Prospective Studies on Asthma in Childhood (COPSAC), Herlev and Gentofte Hospital University of Copenhagen Gentofte Denmark

6. Division of Allergy and Clinical Immunology Brigham and Women's Hospital and Harvard Medical School Boston Massachusetts USA

7. Division of Pediatric Pulmonary Medicine, Department of Pediatrics Golisano Children's Hospital and University of Rochester Medical Center Rochester New York USA

Abstract

AbstractBackgroundWhile dysregulated sphingolipid metabolism has been associated with risk of childhood asthma, the specific sphingolipid classes and/or mechanisms driving this relationship remain unclear. We aimed to understand the multifaceted role between sphingolipids and other established asthma risk factors that complicate this relationship.MethodsWe performed targeted LC–MS/MS‐based quantification of 77 sphingolipids in plasma from 997 children aged 6 years from two independent cohorts (VDAART and COPSAC2010). We examined associations of circulatory sphingolipids with childhood asthma, lung function, and three asthma risk factors: functional SNPs in ORMDL3, low vitamin D levels, and reduced gut microbial maturity. Given racial differences between these cohorts, association analyses were performed separately and then meta‐analyzed together.ResultsWe observed elevations in circulatory sphingolipids with asthma phenotypes and risk factors; however, there were differential associations of sphingolipid classes with clinical outcomes and/or risk factors. While elevations from metabolites involved in ceramide recycling and catabolic pathways were associated with asthma and worse lung function [meta p‐value range: 1.863E‐04 to 2.24E‐3], increased ceramide levels were associated with asthma risk factors [meta p‐value range: 7.75E‐5 to .013], but not asthma. Further investigation identified that some ceramides acted as mediators while some interacted with risk factors in the associations with asthma outcomes.ConclusionThis study demonstrates the differential role that sphingolipid subclasses may play in asthma and its risk factors. While overall elevations in sphingolipids appeared to be deleterious overall; elevations in ceramides were uniquely associated with increases in asthma risk factors only; while elevations in asthma phenotypes were associated with recycling sphingolipids. Modification of asthma risk factors may play an important role in regulating sphingolipid homeostasis via ceramides to affect asthma. Further function work may validate the observed associations.

Funder

European Research Council

Japan Society for the Promotion of Science

National Heart, Lung, and Blood Institute

Publisher

Wiley

Subject

Immunology,Immunology and Allergy

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