MicroRNAs 146a/b-5 and 425-3p and 24-3p are markers of antidepressant response and regulate MAPK/Wnt-system genes

Juan Pablo López(Douglas Mental Health University Institute), Laura M. Fiori(Douglas Mental Health University Institute), Cristiana Cruceanu(Douglas Mental Health University Institute), Rixing Lin(Douglas Mental Health University Institute), Benoît Labonté(Allen Institute for Brain Science), Hannah M. Cates(Allen Institute for Brain Science), Elizabeth A. Heller(Allen Institute for Brain Science), Vincent Vialou(Allen Institute for Brain Science), Stacy M. Ku(Allen Institute for Brain Science), Christophe Gerald(Allen Institute for Brain Science), Ming-Hu Han(Allen Institute for Brain Science), Jane A. Foster(University Health Network), Benício N. Frey(St. Joseph’s Healthcare Hamilton), Claudio N. Soares(St. Michael's Hospital), Daniel J. Müller(University Health Network), Faranak Farzan(University Health Network), Francesco Leri(University of Guelph), Glenda MacQueen(University of Calgary), Harriet Feilotter(Queen's University), Kathrin Tyryshkin(Queen's University), Kenneth Evans(Queen's University), Peter Giacobbe(University Health Network), Pierre Blier(University of Ottawa), Raymond W. Lam(Vancouver Coastal Health), Roumen Milev(Queen's University), Sagar V. Parikh(University of Michigan), Susan Rotzinger(University Health Network), Stephen C. Strother(Baycrest Hospital), Cathryn M. Lewis(King's College London), Katherine J. Aitchison(Dalhousie University), Gayle Wittenberg(Janssen (Belgium)), Naguib Mechawar(Douglas Mental Health University Institute), Eric J. Nestler(Allen Institute for Brain Science), Rudolf Uher(Dalhousie University), Sidney H. Kennedy(University Health Network), Gustavo Turecki(Douglas Mental Health University Institute)
Nature Communications
May 22, 2017
Cited by 205Open Access
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Abstract

Antidepressants (ADs) are the most common treatment for major depressive disorder (MDD). However, only ∼30% of patients experience adequate response after a single AD trial, and this variability remains poorly understood. Here, we investigated microRNAs (miRNAs) as biomarkers of AD response using small RNA-sequencing in paired samples from MDD patients enrolled in a large, randomized placebo-controlled trial of duloxetine collected before and 8 weeks after treatment. Our results revealed differential expression of miR-146a-5p, miR-146b-5p, miR-425-3p and miR-24-3p according to treatment response. These results were replicated in two independent clinical trials of MDD, a well-characterized animal model of depression, and post-mortem human brains. Furthermore, using a combination of bioinformatics, mRNA studies and functional in vitro experiments, we showed significant dysregulation of genes involved in MAPK/Wnt signalling pathways. Together, our results indicate that these miRNAs are consistent markers of treatment response and regulators of the MAPK/Wnt systems.


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