4.8 Article

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

Journal

NATURE COMMUNICATIONS
Volume 8, Issue -, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/ncomms15497

Keywords

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Funding

  1. Ontario Brain Institute
  2. Ontario government
  3. Canadian Institute of Health Research (CIHR) [MOP93775, MOP11260, MOP119429, MOP119430]
  4. US National Institutes of Health (NIH) [1R01DA033684]
  5. Fonds de Recherche du Quebec - Sante (FRQS) through Chercheur National salary award
  6. Fonds de Recherche du Quebec - Sante (FRQS) through Quebec Network on Suicide, Mood Disorders and Related Disorders
  7. Frederick Banting Graduate Scholarship
  8. Charles Best Canada Graduate Scholarship
  9. CIHR
  10. National Institute of Mental Health (NIMH)
  11. European Commission [LSHB-CT-2003-503428]
  12. Government of Alberta - Alberta Centennial Addiction and Mental Health Research Chair
  13. Canada Research Chair program
  14. National Institute for Health Research (NIHR) Biomedical Research Centre at South London and Maudsley NHS Foundation Trust and King's College London
  15. Canadian Institutes of Health Research (CIHR)
  16. Brain Canada
  17. Lundbeck
  18. Bristol-Myers Squibb
  19. Pfizer
  20. Servier

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Antidepressants (ADs) are the most common treatment for major depressive disorder (MDD). However, only similar to 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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