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Analysis of the influence of microRNAs in lithium response in bipolar disorder

  • Céline S. Reinbold
  • , Andreas J. Forstner
  • , Julian Hecker
  • , Janice M. Fullerton
  • , Per Hoffmann
  • , Liping Hou
  • , Urs Heilbronner
  • , Franziska Degenhardt
  • , Mazda Adli
  • , Kazufumi Akiyama
  • , Nirmala Akula
  • , Raffaella Ardau
  • , Bárbara Arias
  • , Lena Backlund
  • , Antonio Benabarre
  • , Susanne Bengesser
  • , Abesh K. Bhattacharjee
  • , Joanna M. Biernacka
  • , Armin Birner
  • , Cynthia Marie-Claire
  • Pablo Cervantes, Guo Bo Chen, Hsi Chung Chen, Caterina Chillotti, Scott R. Clark, Francesc Colom, David A. Cousins, Cristiana Cruceanu, Piotr M. Czerski, Alexandre Dayer, Bruno Étain, Peter Falkai, Louise Frisén, Sébastien Gard, Julie S. Garnham, Fernando S. Goes, Paul Grof, Oliver Gruber, Ryota Hashimoto, Joanna Hauser, Stefan Herms, Stéphane Jamain, Esther Jiménez, Jean Pierre Kahn, Layla Kassem, Sarah Kittel-Schneider, Sebastian Kliwicki, Barbara König, Ichiro Kusumi, Nina Lackner, Gonzalo Laje, Mikael Landén, Catharina Lavebratt, Marion Leboyer, Susan G. Leckband, Carlos A.López Jaramillo, Glenda MacQueen, Mirko Manchia, Lina Martinsson, Manuel Mattheisen, Michael J. McCarthy, Susan L. McElroy, Marina Mitjans, Francis M. Mondimore, Palmiero Monteleone, Caroline M. Nievergelt, Urban Ösby, Norio Ozaki, Roy H. Perlis, Andrea Pfennig, Daniela Reich-Erkelenz, Guy A. Rouleau, Peter R. Schofield, K. Oliver Schubert, Barbara W. Schweizer, Florian Seemüller, Giovanni Severino, Tatyana Shekhtman, Paul D. Shilling, Kazutaka Shimoda, Christian Simhandl, Claire M. Slaney, Jordan W. Smoller, Alessio Squassina, Thomas J. Stamm, Pavla Stopkova, Sarah K. Tighe, Alfonso Tortorella, Gustavo Turecki, Julia Volkert, Stephanie H. Witt, Adam J. Wright, L. Trevor Young, Peter P. Zandi, James B. Potash, J. Raymond DePaulo, Michael Bauer, Eva Reininghaus, Tomáš Novák, Jean Michel Aubry, Mario Maj, Bernhard T. Baune, Philip B. Mitchell, Eduard Vieta, Mark A. Frye, Janusz K. Rybakowski, Po Hsiu Kuo, Tadafumi Kato, Maria Grigoroiu-Serbanescu, Andreas Reif, Maria Del Zompo, Frank Bellivier, Martin Schalling, Naomi R. Wray, John R. Kelsoe, Martin Alda, Francis J. McMahon, Thomas G. Schulze, Marcella Rietschel, Markus M. Nöthen, Sven Cichon
  • University of Basel
  • University of Bonn
  • Harvard University
  • Neuroscience Research Australia
  • University of New South Wales
  • National Institutes of Health
  • Ludwig Maximilian University of Munich
  • Charité – Universitätsmedizin Berlin
  • Dokkyo Medical University
  • University Hospital of Cagliari
  • University of Barcelona
  • Karolinska Institutet
  • Medical University of Graz
  • Mayo Clinic Rochester, MN
  • Institut national de la santé et de la recherche médicale
  • Université Paris Cité
  • University of California at San Diego
  • McGill University
  • University of Queensland
  • National Taiwan University
  • University of Adelaide
  • Hospital del Mar
  • Newcastle University
  • Douglas Mental Health University Institute
  • University of Medical Sciences Poznan
  • University of Geneva
  • Assistance publique – Hôpitaux de Paris
  • Hôpital Charles Perrens
  • Dalhousie University
  • Johns Hopkins University
  • Mood Disorders Center Ottawa
  • University of Göttingen
  • The University of Osaka
  • Psychiatrie Translationnelle
  • Université de Lorraine
  • Goethe University Frankfurt
  • Landesklinikum Neunkirchen
  • Hokkaido University
  • University of Gothenburg
  • Department of Veterans Affairs
  • Universidad de Antioquia
  • University of Calgary
  • University of Cagliari
  • Aarhus University
  • University of Cincinnati
  • University of Salerno
  • University of Campania Luigi Vanvitelli
  • Nagoya University
  • Massachusetts General Hospital
  • Technische Universität Dresden
  • Sigmund Freud University Vienna
  • Bipolar Center Wiener Neustadt
  • Brandenburg Medical School Theodor Fontane
  • National Institute of Mental Health
  • University of Iowa
  • Heidelberg University 
  • University of British Columbia
  • RIKEN
  • Alexandru Obregia Clinical Psychiatric Hospital
  • Jülich Research Centre

Research output: Contribution to journalArticlepeer-review

Abstract

Bipolar disorder (BD) is a common, highly heritable neuropsychiatric disease characterized by recurrent episodes of mania and depression. Lithium is the best-established long-term treatment for BD, even though individual response is highly variable. Evidence suggests that some of this variability has a genetic basis. This is supported by the largest genome-wide association study (GWAS) of lithium response to date conducted by the International Consortium on Lithium Genetics (ConLiGen). Recently, we performed the first genome-wide analysis of the involvement of miRNAs in BD and identified nine BD-associated miRNAs. However, it is unknown whether these miRNAs are also associated with lithium response in BD. In the present study, we therefore tested whether common variants at these nine candidate miRNAs contribute to the variance in lithium response in BD. Furthermore, we systematically analyzed whether any other miRNA in the genome is implicated in the response to lithium. For this purpose, we performed gene-based tests for all known miRNA coding genes in the ConLiGen GWAS dataset (n = 2,563 patients) using a set-based testing approach adapted from the versatile gene-based test for GWAS (VEGAS2). In the candidate approach, miR-499a showed a nominally significant association with lithium response, providing some evidence for involvement in both development and treatment of BD. In the genome-wide miRNA analysis, 71 miRNAs showed nominally significant associations with the dichotomous phenotype and 106 with the continuous trait for treatment response. A total of 15 miRNAs revealed nominal significance in both phenotypes with miR-633 showing the strongest association with the continuous trait (p = 9.80E-04) and miR-607 with the dichotomous phenotype (p = 5.79E-04). No association between miRNAs and treatment response to lithium in BD in either of the tested conditions withstood multiple testing correction. Given the limited power of our study, the investigation of miRNAs in larger GWAS samples of BD and lithium response is warranted.

Original languageEnglish
Article number207
JournalFrontiers in Psychiatry
Volume9
Issue numberMAY
DOIs
Publication statusPublished - 31 May 2018
Externally publishedYes

Keywords

  • Bipolar disorder
  • Common variants
  • Genome-wide association study
  • Lithium response
  • MicroRNA

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