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Epigenetic signature for attention-deficit/hyperactivity disorder: identification of miR-26b-5p, miR-185-5p, and miR-191-5p as potential biomarkers in peripheral blood mononuclear cells

Authors :
Iris Garcia-Martínez
Marta Ribasés
Paula Rovira
Vanesa Richarte
Montse Corrales
Natalia Padilla
Christian Fadeuilhe
Alejandro Arias-Vasquez
Miguel Casas
Cristina Sánchez-Mora
Xavier de la Cruz
Barbara Franke
Josep Antoni Ramos-Quiroga
Mireia Pagerols
María Soler Artigas
Source :
Neuropsychopharmacology, Neuropsychopharmacology, 44, 890-897, Neuropsychopharmacology, 44, 5, pp. 890-897
Publication Year :
2019

Abstract

Attention-deficit/hyperactivity disorder (ADHD) is one of the most prevalent neurodevelopmental disorders in childhood and persists into adulthood in 40-65% of cases. Given the polygenic and heterogeneous architecture of the disorder and the limited overlap between genetic studies, there is a growing interest in epigenetic mechanisms, such as microRNAs, that modulate gene expression and may contribute to the phenotype. We attempted to clarify the role of microRNAs in ADHD at a molecular level through the first genome-wide integrative study of microRNA and mRNA profiles in peripheral blood mononuclear cells of medication-naive individuals with ADHD and healthy controls. We identified 79 microRNAs showing aberrant expression levels in 56 ADHD cases and 69 controls, with three of them, miR-26b-5p, miR-185-5p, and miR-191-5p, being highly predictive for diagnostic status in an independent dataset of 44 ADHD cases and 46 controls. Investigation of downstream microRNA-mediated mechanisms underlying the disorder, which was focused on differentially expressed, experimentally validated target genes of the three highly predictive microRNAs, provided evidence for aberrant myo-inositol signaling in ADHD and indicated an enrichment of genes involved in neurological disease and psychological disorders. Our comprehensive study design reveals novel microRNA-mRNA expression profiles aberrant in ADHD, provides novel insights into microRNA-mediated mechanisms contributing to the disorder, and highlights promising candidate peripheral biomarkers.

Details

ISSN :
0893133X
Database :
OpenAIRE
Journal :
Neuropsychopharmacology
Accession number :
edsair.doi.dedup.....88ede8f0eb4003ef41d8fc281620471d
Full Text :
https://doi.org/10.1038/s41386-018-0297-0