The German research consortium for the study of bipolar disorder (BipoLife): a magnetic resonance imaging study protocol

Background: Bipolar disorder is one of the most severe mental disorders. Its chronic course is associated with high rates of morbidity and mortality, a high risk of suicide and poor social and occupational outcomes. Despite the great advances over the last decades in understanding mental disorders, the mechanisms underlying bipolar disorder at the neural network level still remain elusive. This has severe consequences for clinical practice, for instance by inadequate diagnoses or delayed treatments. The German research consortium BipoLife aims to shed light on the mechanisms underlying bipolar disorders. It was established in 2015 and incorporates ten university hospitals across Germany. Its research projects focus in particular on individuals at high risk of bipolar disorder, young patients in the early stages of the disease and patients with an unstable highly relapsing course and/or with acute suicidal ideation. Methods: Functional and structural magnetic resonance imaging (MRI) data was acquired across nine sites within three different studies. Obtaining neuroimaging data in a multicenter setting requires among others the harmonization of the acquisition protocol, the standardization of paradigms and the implementation of regular quality control procedures. The present article outlines the MRI imaging protocols, the acquisition parameters, the imaging paradigms, the neuroimaging quality assessment procedures and the number of recruited subjects.Discussion: The careful implementation of a MRI study protocol as well as the adherence to well-defined quality assessment procedures is one key benchmark in the evaluation of the overall quality of large-scale multicenter imaging studies. This article contributes to the BipoLife project by outlining the rationale and the design of the MRI study protocol. It helps to set the necessary standards for follow-up analyses and provides the technical details for an in-depth understanding of follow-up publications.

[1]  A. Duffy The nature of the association between childhood ADHD and the development of bipolar disorder: a review of prospective high-risk studies. , 2012, The American journal of psychiatry.

[2]  T. Schulze,et al.  Aims and structure of the German Research Consortium BipoLife for the study of bipolar disorder , 2016, International Journal of Bipolar Disorders.

[3]  A. Toga,et al.  Multisite neuroimaging trials , 2009, Current opinion in neurology.

[4]  Satrajit S. Ghosh,et al.  The brain imaging data structure, a format for organizing and describing outputs of neuroimaging experiments , 2016, Scientific Data.

[5]  P. Ekman An argument for basic emotions , 1992 .

[6]  P. Falkai,et al.  A functional neuroimaging study assessing gender differences in the neural mechanisms underlying the ability to resist impulsive desires , 2012, Brain Research.

[7]  Michele T. Diaz,et al.  Function biomedical informatics research network recommendations for prospective multicenter functional MRI studies , 2012, Journal of magnetic resonance imaging : JMRI.

[8]  Krzysztof J. Gorgolewski,et al.  MRIQC: Advancing the automatic prediction of image quality in MRI from unseen sites , 2016, bioRxiv.

[9]  Christoph Vogelbacher,et al.  LAB–QA2GO: A Free, Easy-to-Use Toolbox for the Quality Assessment of Magnetic Resonance Imaging Data , 2019, bioRxiv.

[10]  R. C. Oldfield The assessment and analysis of handedness: the Edinburgh inventory. , 1971, Neuropsychologia.

[11]  P. Sham,et al.  The heritability of bipolar affective disorder and the genetic relationship to unipolar depression. , 2003, Archives of general psychiatry.

[12]  S Cichon,et al.  Effects of a genome-wide supported psychosis risk variant on neural activation during a theory-of-mind task , 2011, Molecular Psychiatry.

[13]  A. Jansen,et al.  Brain structural correlates of schizotypal signs and subclinical schizophrenia nuclear symptoms in healthy individuals , 2020, Psychological Medicine.

[14]  P. Falkai,et al.  Disturbed Anterior Prefrontal Control of the Mesolimbic Reward System and Increased Impulsivity in Bipolar Disorder , 2014, Neuropsychopharmacology.

[15]  M. Höfler,et al.  Symptom characteristics of depressive episodes prior to the onset of mania or hypomania , 2016, Acta psychiatrica Scandinavica.

[16]  J. Reichenbach,et al.  Brain structure in people at ultra-high risk of psychosis, patients with first-episode schizophrenia, and healthy controls: a VBM study , 2015, Schizophrenia Research.

[17]  Francesco Fera,et al.  The Amygdala Response to Emotional Stimuli: A Comparison of Faces and Scenes , 2002, NeuroImage.

[18]  D. Kupfer,et al.  Diagnostic Precursors to Bipolar Disorder in Offspring of Parents With Bipolar Disorder: A Longitudinal Study. , 2015, The American journal of psychiatry.

[19]  G. Juckel,et al.  Does lithium reduce acute suicidal ideation and behavior? A protocol for a randomized, placebo-controlled multicenter trial of lithium plus Treatment As Usual (TAU) in patients with suicidal major depressive episode , 2015, BMC Psychiatry.

[20]  Tilo Kircher,et al.  The Marburg-Münster Affective Disorders Cohort Study (MACS): A quality assurance protocol for MR neuroimaging data , 2018, NeuroImage.

[21]  Improving early recognition and intervention in people at increased risk for the development of bipolar disorder: study protocol of a prospective-longitudinal, naturalistic cohort study (Early-BipoLife) , 2020, International Journal of Bipolar Disorders.

[22]  A. Jansen,et al.  Long-Term Neuroanatomical Consequences of Childhood Maltreatment: Reduced Amygdala Inhibition by Medial Prefrontal Cortex , 2020, Frontiers in Systems Neuroscience.

[23]  M. Hautzinger,et al.  Adjuvant psychotherapy in early-stage bipolar disorder: study protocol for a randomized controlled trial , 2020, Trials.

[24]  Lee Friedman,et al.  Report on a multicenter fMRI quality assurance protocol , 2006, Journal of magnetic resonance imaging : JMRI.

[25]  J. Paris,et al.  The developmental trajectory of bipolar disorder , 2014, British Journal of Psychiatry.

[26]  Oliver Gruber,et al.  When Desire Collides with Reason: Functional Interactions between Anteroventral Prefrontal Cortex and Nucleus Accumbens Underlie the Human Ability to Resist Impulsive Desires , 2009, The Journal of Neuroscience.