Specific microRNA Profile Associated with Inflammation and Lipid Metabolism for Stratifying Allergic Asthma Severity

Author:

Escolar-Peña Andrea1ORCID,Delgado-Dolset María Isabel1ORCID,Pablo-Torres Carmela1,Tarin Carlos2ORCID,Mera-Berriatua Leticia1,Cuesta Apausa María del Pilar3,González Cuervo Heleia3,Sharma Rinku4ORCID,Kho Alvin T.5ORCID,Tantisira Kelan G.6,McGeachie Michael J.4,Rebollido-Rios Rocio789ORCID,Barber Domingo1ORCID,Carrillo Teresa3,Izquierdo Elena1,Escribese María M.1ORCID

Affiliation:

1. Department of Basic Medical Sciences, Institute for Applied Molecular Medicine Nemesio Díez, School of Medicine, Universidad San Pablo-CEU, CEU Universities, Urbanización Montepríncipe, 28668 Boadilla del Monte, Spain

2. R+D Department, Atrys Health, 08025 Madrid, Spain

3. Allergy Service, Hospital Universitario de Gran Canaria Doctor Negrín, 35010 Las Palmas de Gran Canaria, Spain

4. Department of Medicine, Channing Division of Network Medicine, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA 02115, USA

5. Computational Health Informatics Program, Boston Children’s Hospital, Boston, MA 02115, USA

6. Division of Pediatric Respiratory Medicine, University of California San Diego and Rady Children’s Hospital, San Diego, CA 92123, USA

7. Department I of Internal Medicine, Centre of Integrated Oncology Aachen Bonn Cologne Duesseldorf (CIO ABCD), Faculty of Medicine and University Hospital of Cologne, University of Cologne, 50923 Cologne, Germany

8. Center for Molecular Medicine Cologne, University of Cologne, 50923 Cologne, Germany

9. CECAD Center of Excellence on Cellular Stress Responses in Aging-Associated Diseases, University of Cologne, 50923 Cologne, Germany

Abstract

The mechanisms underlying severe allergic asthma are complex and unknown, meaning it is a challenge to provide the most appropriate treatment. This study aimed to identify novel biomarkers for stratifying allergic asthmatic patients according to severity, and to uncover the biological mechanisms that lead to the development of the severe uncontrolled phenotype. By using miRNA PCR panels, we analyzed the expression of 752 miRNAs in serum samples from control subjects (n = 15) and mild (n = 11) and severe uncontrolled (n = 10) allergic asthmatic patients. We identified 40 differentially expressed miRNAs between severe uncontrolled and mild allergic asthmatic patients. Functional enrichment analysis revealed signatures related to inflammation, angiogenesis, lipid metabolism and mRNA regulation. A random forest classifier trained with DE miRNAs achieved a high accuracy of 97% for severe uncontrolled patient stratification. Validation of the identified biomarkers was performed on a subset of allergic asthmatic patients from the CAMP cohort at Brigham and Women’s Hospital, Harvard Medical School. Four of these miRNAs (hsa-miR-99b-5p, hsa-miR-451a, hsa-miR-326 and hsa-miR-505-3p) were validated, pointing towards their potential as biomarkers for stratifying allergic asthmatic patients by severity and providing insights into severe uncontrolled asthma molecular pathways.

Funder

ISCIII

FEDER

Fundación Mutua Madrileña

FPI-CEU predoctoral fellowships

National Institute of Health

Publisher

MDPI AG

Reference65 articles.

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