<p>MRI studies in bipolar disorder (BD) have yielded inconsistent findings, partly due to the varied use of psychotropic medications. This study utilised a mega-analysis approach, accounting for concurrent medication status (syndrome-based and Neuroscience-based Nomenclature (NbN) classifications), in order to assess the association of medication status with subcortical brain volumes in BD. Data from 2,664 BD patients and 4,065 controls (CN) were pooled from 34 research groups as part of the ENIGMA Bipolar Disorder Working Group. Standardized ENIGMA protocols were used to measure subcortical brain volumes. Linear-mixed-effects regression evaluated the association between psychotropic medications and subcortical volumes, and moderation analyses explored interactions. Medication-free patients (n = 410) showed mild ventricular enlargement (d = 0.07) and increased putamen volume (d = 0.06) compared to CN. Patients taking psychotropic medications exhibited smaller subcortical volumes (d = -0.06 to -0.11) and larger ventricles (d = 0.11 to 0.19). Use of antiepileptic and antipsychotic medications was associated with smaller hippocampal and thalamic volumes (d = -0.07 to -0.14), while NbN classification indicated that the categories of ‘valproate’ and ‘dopamine and other monoamine receptor antagonists’ are key variables when considering volume differences between BD and CN. Concurrent lithium use weakened the negative association between antiepileptic use and hippocampal volume (β = 0.19, q = 0.038) in patients. Medication status is associated with altered subcortical brain volumes in BD. The NbN classification provides a useful framework for future studies, emphasizing the need for comprehensive longitudinal research to further unravel complex clinical-pharmacological-neurobiological interactions in BD.</p>

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Psychotropic medications and their interactions with subcortical brain volume in bipolar disorder: An ENIGMA mega-analysis

  • Sinead King,
  • John O’Connor,
  • Emma Corley,
  • Giulia Tronchin,
  • Elisa Fontana,
  • Leila Nabulsi,
  • Melody J. Y. Kang,
  • Joaquim Radua,
  • Brian Hallahan,
  • Christoph Abé,
  • Martin Alda,
  • Dag Alnæs,
  • Silvia Alonso-Lana,
  • Silvia Amoretti,
  • Jochen Bauer,
  • Francesco Benedetti,
  • Klaus Berger,
  • Michael Berk,
  • Erlend Bøen,
  • Joscha Böhnlein,
  • Birgitte Boye,
  • Beatrice Bravi,
  • Erick J. Canales-Rodríguez,
  • Udo Dannlowski,
  • Caroline Demro,
  • Annabella Di Giorgio,
  • Ana M. Diaz-Zuluaga,
  • Torbjørn Elvsåshagen,
  • Pauline Favre,
  • Tracy Erwin-Grabner,
  • María Florencia Forte,
  • Janice M. Fullerton,
  • Lisa S. Furlong,
  • Susan L. Rossell,
  • David C. Glahn,
  • Benjamin I. Goldstein,
  • Ian H. Gotlib,
  • Roberto Goya-Maldonado,
  • Melissa J. Green,
  • Dominik Grotegerd,
  • Oliver Gruber,
  • Bartholomeus C. M. Haarman,
  • Tim Hahn,
  • Tomas Hajek,
  • Leonie Hater,
  • Marco Hermesdorf,
  • Josselin Houenou,
  • Fleur M. Howells,
  • James A. Karantonis,
  • Kody G. Kennedy,
  • Tilo Kircher,
  • Anna Luisa Klahn,
  • Maximilian Konowski,
  • Bernd Krämer,
  • Elijah Lahud,
  • Rayus Kuplicki,
  • Mikael Landén,
  • Carlos López-Jaramillo,
  • Bradley J. MacIntosh,
  • Hannah Meinert,
  • Susanne Meinert,
  • Elisa M. T. Melloni,
  • Philip B. Mitchell,
  • Benson Mwangi,
  • Igor Nenadić,
  • Bronwyn J. Overs,
  • Nadine Parker,
  • Godfrey Pearlson,
  • Edith Pomarol-Clotet,
  • James J. Prisciandaro,
  • Yann Quidé,
  • Gloria Roberts,
  • Amanda Rodrigue,
  • Elena Rodríguez-Cano,
  • Lisa Rauer,
  • Matthew D. Sacchet,
  • Raymond Salvador,
  • Fabio Sambataro,
  • Theodore D. Satterthwaite,
  • Jonathan Savitz,
  • Freda Scheffler,
  • Navid Schürmeyer,
  • Chen Shen,
  • Kang Sim,
  • Jair C. Soares,
  • Aleix Solanes,
  • Márcio Gerhardt Soeiro-de-Souza,
  • Scott R. Sponheim,
  • Dan J. Stein,
  • Frederike Stein,
  • Henk S. Temmingh,
  • Lea Teutenberg,
  • Sophia I. Thomopoulos,
  • Snezana Urosevic,
  • Tamsyn E. Van Rheenen,
  • Eduard Vieta,
  • Lars T. Westlye,
  • Daniel H. Wolf,
  • Mon-Ju Wu,
  • Lakshmi N. Yatham,
  • Giovana B. Zunta-Soares,
  • Dara M. Cannon,
  • Paul M. Thompson,
  • Ole A. Andreassen,
  • Christopher R. K. Ching,
  • Colm McDonald,
  • Annabella Di Giorgio,
  • Tamsyn E. Van Rheenen

摘要

MRI studies in bipolar disorder (BD) have yielded inconsistent findings, partly due to the varied use of psychotropic medications. This study utilised a mega-analysis approach, accounting for concurrent medication status (syndrome-based and Neuroscience-based Nomenclature (NbN) classifications), in order to assess the association of medication status with subcortical brain volumes in BD. Data from 2,664 BD patients and 4,065 controls (CN) were pooled from 34 research groups as part of the ENIGMA Bipolar Disorder Working Group. Standardized ENIGMA protocols were used to measure subcortical brain volumes. Linear-mixed-effects regression evaluated the association between psychotropic medications and subcortical volumes, and moderation analyses explored interactions. Medication-free patients (n = 410) showed mild ventricular enlargement (d = 0.07) and increased putamen volume (d = 0.06) compared to CN. Patients taking psychotropic medications exhibited smaller subcortical volumes (d = -0.06 to -0.11) and larger ventricles (d = 0.11 to 0.19). Use of antiepileptic and antipsychotic medications was associated with smaller hippocampal and thalamic volumes (d = -0.07 to -0.14), while NbN classification indicated that the categories of ‘valproate’ and ‘dopamine and other monoamine receptor antagonists’ are key variables when considering volume differences between BD and CN. Concurrent lithium use weakened the negative association between antiepileptic use and hippocampal volume (β = 0.19, q = 0.038) in patients. Medication status is associated with altered subcortical brain volumes in BD. The NbN classification provides a useful framework for future studies, emphasizing the need for comprehensive longitudinal research to further unravel complex clinical-pharmacological-neurobiological interactions in BD.