Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/176667
Title: What we learn about bipolar disorder from large-scale neuroimaging: Findings and future directions from the ENIGMA Bipolar Disorder Working Group
Author: Ching, Christopher R. K.
Hibar, Derrek P.
Gurholt, Tiril P.
Nunes, Abraham
Thomopoulos, Sophia I.
Abé, Christoph
Agartz, Ingrid
Brouwer, Rachel M.
Cannon, Dara M.
de Zwarte, Sonja M.C.
Eyler, Lisa T.
Favre, Pauline
Hajek, Tomas
Haukvik, Unn K.
Houenou, Josselin
Landén, Mikael
Lett, Tristram A.
McDonald, Colm
Nabulsi, Leila
Patel, Yash
Pauling, Melissa E.
Paus, Tomas
Radua, Joaquim
Soeiro-de-Souza, MarcioG.
Tronchin, Giulia
van Haren, Neeltje E.M.
Vieta i Pascual, Eduard, 1963-
Walter, Henrik
Zeng, Ling-Li
Alda, Martin
Almeida, Jorge
Alnæs, Dag
Alonso Lana, Silvia
Altimus, Cara
Bauer, Michael
Baune, Bernhard T.
Bearden, Carrie E.
Bellani, Marcella
Bonnín, Caterina del Mar
ENIGMA Bipolar Disorder Working Group
Keywords: Imatges per ressonància magnètica
Trastorn bipolar
Magnetic resonance imaging
Manic-depressive illness
Issue Date: 29-Jul-2020
Publisher: Wiley
Abstract: MRI‐derived brain measures offer a link between genes, the environment and behavior and have been widely studied in bipolar disorder (BD). However, many neuroimaging studies of BD have been underpowered, leading to varied results and uncertainty regarding effects. The Enhancing Neuro Imaging Genetics through Meta‐Analysis (ENIGMA) Bipolar Disorder Working Group was formed in 2012 to empower discoveries, generate consensus findings and inform future hypothesis‐driven studies of BD. Through this effort, over 150 researchers from 20 countries and 55 institutions pool data and resources to produce the largest neuroimaging studies of BD ever conducted. The ENIGMA Bipolar Disorder Working Group applies standardized processing and analysis techniques to empower large‐scale meta‐ and mega‐analyses of multimodal brain MRI and improve the replicability of studies relating brain variation to clinical and genetic data. Initial BD Working Group studies reveal widespread patterns of lower cortical thickness, subcortical volume and disrupted white matter integrity associated with BD. Findings also include mapping brain alterations of common medications like lithium, symptom patterns and clinical risk profiles and have provided further insights into the pathophysiological mechanisms of BD. Here we discuss key findings from the BD working group, its ongoing projects and future directions for large‐scale, collaborative studies of mental illness.
Note: Reproducció del document publicat a: https://doi.org/10.1002/hbm.25098
It is part of: Human Brain Mapping, 2020
URI: http://hdl.handle.net/2445/176667
Related resource: https://doi.org/10.1002/hbm.25098
ISSN: 1065-9471
Appears in Collections:Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)
Articles publicats en revistes (Medicina)
Publicacions de projectes de recerca finançats per la UE

Files in This Item:
File Description SizeFormat 
702899.pdf6.73 MBAdobe PDFView/Open


This item is licensed under a Creative Commons License Creative Commons