Sphingolipids in Childhood Asthma and Obesity (SOAP Study): A Protocol of a Cross-Sectional Study

Asthma and obesity are two of the most common chronic conditions in children and adolescents. There is increasing evidence that sphingolipid metabolism is altered in childhood asthma and is linked to airway hyperreactivity. Dysregulated sphingolipid metabolism is also reported in obesity. However, t...

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Main Authors: Belavendra Antonisamy, Harshita Shailesh, Yahya Hani, Lina Hayati M. Ahmed, Safa Noor, Salma Yahya Ahmed, Mohamed Alfaki, Abidan Muhayimana, Shana Sunny Jacob, Saroja Kotegar Balayya, Oleksandr Soloviov, Li Liu, Lisa Sara Mathew, Kun Wang, Sara Tomei, Alia Al Massih, Rebecca Mathew, Mohammed Yousuf Karim, Manjunath Ramanjaneya, Stefan Worgall, Ibrahim A. Janahi
Format: Article
Language:English
Published: MDPI AG 2023-11-01
Series:Metabolites
Subjects:
Online Access:https://www.mdpi.com/2218-1989/13/11/1146
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author Belavendra Antonisamy
Harshita Shailesh
Yahya Hani
Lina Hayati M. Ahmed
Safa Noor
Salma Yahya Ahmed
Mohamed Alfaki
Abidan Muhayimana
Shana Sunny Jacob
Saroja Kotegar Balayya
Oleksandr Soloviov
Li Liu
Lisa Sara Mathew
Kun Wang
Sara Tomei
Alia Al Massih
Rebecca Mathew
Mohammed Yousuf Karim
Manjunath Ramanjaneya
Stefan Worgall
Ibrahim A. Janahi
author_facet Belavendra Antonisamy
Harshita Shailesh
Yahya Hani
Lina Hayati M. Ahmed
Safa Noor
Salma Yahya Ahmed
Mohamed Alfaki
Abidan Muhayimana
Shana Sunny Jacob
Saroja Kotegar Balayya
Oleksandr Soloviov
Li Liu
Lisa Sara Mathew
Kun Wang
Sara Tomei
Alia Al Massih
Rebecca Mathew
Mohammed Yousuf Karim
Manjunath Ramanjaneya
Stefan Worgall
Ibrahim A. Janahi
author_sort Belavendra Antonisamy
collection DOAJ
description Asthma and obesity are two of the most common chronic conditions in children and adolescents. There is increasing evidence that sphingolipid metabolism is altered in childhood asthma and is linked to airway hyperreactivity. Dysregulated sphingolipid metabolism is also reported in obesity. However, the functional link between sphingolipid metabolism, asthma, and obesity is not completely understood. This paper describes the protocol of an ongoing study on sphingolipids that aims to examine the pathophysiology of sphingolipids in childhood asthma and obesity. In addition, this study aims to explore the novel biomarkers through a comprehensive multi-omics approach including genomics, genome-wide DNA methylation, RNA-Seq, microRNA (miRNA) profiling, lipidomics, metabolomics, and cytokine profiling. This is a cross-sectional study aiming to recruit 440 children from different groups: children with asthma and normal weight (<i>n</i> = 100), asthma with overweight or obesity (<i>n</i> = 100), overweight or obesity (<i>n</i> = 100), normal weight (<i>n</i> = 70), and siblings of asthmatic children with normal weight, overweight, or obesity (<i>n</i> = 70). These participants will be recruited from the pediatric pulmonology, pediatric endocrinology, and general pediatric outpatient clinics at Sidra Medicine, Doha, Qatar. Information will be obtained from self-reported questionnaires on asthma, quality of life, food frequency (FFQ), and a 3-day food diary that are completed by the children and their parents. Clinical measurements will include anthropometry, blood pressure, biochemistry, bioelectrical impedance, and pulmonary function tests. Blood samples will be obtained for sphingolipid analysis, serine palmitoyltransferase (SPT) assay, whole-genome sequencing (WGS), genome-wide DNA methylation study, RNA-Seq, miRNA profiling, metabolomics, lipidomics, and cytokine analysis. Group comparisons of continuous outcome variables will be carried out by a one-way analysis of variance or the Kruskal–Wallis test using an appropriate pairwise multiple comparison test. The chi-squared test or a Fisher’s exact test will be used to test the associations between categorical variables. Finally, multivariate analysis will be carried out to integrate the clinical data with multi-omics data. This study will help us to understand the role of dysregulated sphingolipid metabolism in obesity and asthma. In addition, the multi-omics data from the study will help to identify novel genetic and epigenetic signatures, inflammatory markers, and mechanistic pathways that link asthma and obesity in children. Furthermore, the integration of clinical and multi-omics data will help us to uncover the potential interactions between these diseases and to offer a new paradigm for the treatment of pediatric obesity-associated asthma.
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spelling doaj.art-3b3f55e70637419aa7c7ccebe36915932023-11-24T14:55:29ZengMDPI AGMetabolites2218-19892023-11-011311114610.3390/metabo13111146Sphingolipids in Childhood Asthma and Obesity (SOAP Study): A Protocol of a Cross-Sectional StudyBelavendra Antonisamy0Harshita Shailesh1Yahya Hani2Lina Hayati M. Ahmed3Safa Noor4Salma Yahya Ahmed5Mohamed Alfaki6Abidan Muhayimana7Shana Sunny Jacob8Saroja Kotegar Balayya9Oleksandr Soloviov10Li Liu11Lisa Sara Mathew12Kun Wang13Sara Tomei14Alia Al Massih15Rebecca Mathew16Mohammed Yousuf Karim17Manjunath Ramanjaneya18Stefan Worgall19Ibrahim A. Janahi20Department of Pediatric Medicine, Sidra Medicine, Doha P.O. Box 26999, QatarDepartment of Pediatric Medicine, Sidra Medicine, Doha P.O. Box 26999, QatarDepartment of Pediatric Medicine, Sidra Medicine, Doha P.O. Box 26999, QatarDepartment of Pediatric Medicine, Sidra Medicine, Doha P.O. Box 26999, QatarDepartment of Pediatric Medicine, Sidra Medicine, Doha P.O. Box 26999, QatarDepartment of Pediatric Medicine, Sidra Medicine, Doha P.O. Box 26999, QatarDepartment of Pediatric Medicine, Sidra Medicine, Doha P.O. Box 26999, QatarDepartment of Pediatric Medicine, Sidra Medicine, Doha P.O. Box 26999, QatarAnalytical Chemistry Core, Advanced Diagnostic Core Facilities, Sidra Medicine, Doha P.O. Box 26999, QatarAnalytical Chemistry Core, Advanced Diagnostic Core Facilities, Sidra Medicine, Doha P.O. Box 26999, QatarClinical Genomics Laboratory, Integrated Genomics Services, Sidra Medicine, Doha P.O. Box 26999, QatarClinical Genomics Laboratory, Integrated Genomics Services, Sidra Medicine, Doha P.O. Box 26999, QatarClinical Genomics Laboratory, Integrated Genomics Services, Sidra Medicine, Doha P.O. Box 26999, QatarClinical Genomics Laboratory, Integrated Genomics Services, Sidra Medicine, Doha P.O. Box 26999, QatarOmics Core, Integrated Genomics Services, Sidra Medicine, Doha P.O. Box 26999, QatarOmics Core, Integrated Genomics Services, Sidra Medicine, Doha P.O. Box 26999, QatarOmics Core, Integrated Genomics Services, Sidra Medicine, Doha P.O. Box 26999, QatarDepartment of Pathology, Sidra Medicine, Doha P.O. Box 26999, QatarQatar Metabolic Institute, Hamad Medical Corporation, Doha P.O. Box 3050, QatarDepartment of Pediatrics, Weill Cornell Medicine, New York, NY 10021, USADepartment of Pediatric Medicine, Sidra Medicine, Doha P.O. Box 26999, QatarAsthma and obesity are two of the most common chronic conditions in children and adolescents. There is increasing evidence that sphingolipid metabolism is altered in childhood asthma and is linked to airway hyperreactivity. Dysregulated sphingolipid metabolism is also reported in obesity. However, the functional link between sphingolipid metabolism, asthma, and obesity is not completely understood. This paper describes the protocol of an ongoing study on sphingolipids that aims to examine the pathophysiology of sphingolipids in childhood asthma and obesity. In addition, this study aims to explore the novel biomarkers through a comprehensive multi-omics approach including genomics, genome-wide DNA methylation, RNA-Seq, microRNA (miRNA) profiling, lipidomics, metabolomics, and cytokine profiling. This is a cross-sectional study aiming to recruit 440 children from different groups: children with asthma and normal weight (<i>n</i> = 100), asthma with overweight or obesity (<i>n</i> = 100), overweight or obesity (<i>n</i> = 100), normal weight (<i>n</i> = 70), and siblings of asthmatic children with normal weight, overweight, or obesity (<i>n</i> = 70). These participants will be recruited from the pediatric pulmonology, pediatric endocrinology, and general pediatric outpatient clinics at Sidra Medicine, Doha, Qatar. Information will be obtained from self-reported questionnaires on asthma, quality of life, food frequency (FFQ), and a 3-day food diary that are completed by the children and their parents. Clinical measurements will include anthropometry, blood pressure, biochemistry, bioelectrical impedance, and pulmonary function tests. Blood samples will be obtained for sphingolipid analysis, serine palmitoyltransferase (SPT) assay, whole-genome sequencing (WGS), genome-wide DNA methylation study, RNA-Seq, miRNA profiling, metabolomics, lipidomics, and cytokine analysis. Group comparisons of continuous outcome variables will be carried out by a one-way analysis of variance or the Kruskal–Wallis test using an appropriate pairwise multiple comparison test. The chi-squared test or a Fisher’s exact test will be used to test the associations between categorical variables. Finally, multivariate analysis will be carried out to integrate the clinical data with multi-omics data. This study will help us to understand the role of dysregulated sphingolipid metabolism in obesity and asthma. In addition, the multi-omics data from the study will help to identify novel genetic and epigenetic signatures, inflammatory markers, and mechanistic pathways that link asthma and obesity in children. Furthermore, the integration of clinical and multi-omics data will help us to uncover the potential interactions between these diseases and to offer a new paradigm for the treatment of pediatric obesity-associated asthma.https://www.mdpi.com/2218-1989/13/11/1146childrenasthmaobesitysphingolipidsserine palmitoyltransferase
spellingShingle Belavendra Antonisamy
Harshita Shailesh
Yahya Hani
Lina Hayati M. Ahmed
Safa Noor
Salma Yahya Ahmed
Mohamed Alfaki
Abidan Muhayimana
Shana Sunny Jacob
Saroja Kotegar Balayya
Oleksandr Soloviov
Li Liu
Lisa Sara Mathew
Kun Wang
Sara Tomei
Alia Al Massih
Rebecca Mathew
Mohammed Yousuf Karim
Manjunath Ramanjaneya
Stefan Worgall
Ibrahim A. Janahi
Sphingolipids in Childhood Asthma and Obesity (SOAP Study): A Protocol of a Cross-Sectional Study
Metabolites
children
asthma
obesity
sphingolipids
serine palmitoyltransferase
title Sphingolipids in Childhood Asthma and Obesity (SOAP Study): A Protocol of a Cross-Sectional Study
title_full Sphingolipids in Childhood Asthma and Obesity (SOAP Study): A Protocol of a Cross-Sectional Study
title_fullStr Sphingolipids in Childhood Asthma and Obesity (SOAP Study): A Protocol of a Cross-Sectional Study
title_full_unstemmed Sphingolipids in Childhood Asthma and Obesity (SOAP Study): A Protocol of a Cross-Sectional Study
title_short Sphingolipids in Childhood Asthma and Obesity (SOAP Study): A Protocol of a Cross-Sectional Study
title_sort sphingolipids in childhood asthma and obesity soap study a protocol of a cross sectional study
topic children
asthma
obesity
sphingolipids
serine palmitoyltransferase
url https://www.mdpi.com/2218-1989/13/11/1146
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