TY - JOUR
T1 - Widespread white matter microstructural abnormalities in bipolar disorder
T2 - evidence from mega- and meta-analyses across 3033 individuals
AU - for the ENIGMA Bipolar Disorder Working Group
AU - Favre, Pauline
AU - Pauling, Melissa
AU - Stout, Jacques
AU - Hozer, Franz
AU - Sarrazin, Samuel
AU - Abé, Christoph
AU - Alda, Martin
AU - Alloza, Clara
AU - Alonso-Lana, Silvia
AU - Andreassen, Ole A.
AU - Baune, Bernhard T.
AU - Benedetti, Francesco
AU - Busatto, Geraldo F.
AU - Canales-Rodríguez, Erick J.
AU - Caseras, Xavier
AU - Chaim-Avancini, Tiffany Moukbel
AU - Ching, Christopher R.K.
AU - Dannlowski, Udo
AU - Deppe, Michael
AU - Eyler, Lisa T.
AU - Fatjo-Vilas, Mar
AU - Foley, Sonya F.
AU - Grotegerd, Dominik
AU - Hajek, Tomas
AU - Haukvik, Unn K.
AU - Howells, Fleur M.
AU - Jahanshad, Neda
AU - Kugel, Harald
AU - Lagerberg, Trine V.
AU - Lawrie, Stephen M.
AU - Linke, Julia O.
AU - McIntosh, Andrew
AU - Melloni, Elisa M.T.
AU - Mitchell, Philip B.
AU - Polosan, Mircea
AU - Pomarol-Clotet, Edith
AU - Repple, Jonathan
AU - Roberts, Gloria
AU - Roos, Annerine
AU - Rosa, Pedro G.P.
AU - Salvador, Raymond
AU - Sarró, Salvador
AU - Schofield, Peter R.
AU - Serpa, Mauricio H.
AU - Sim, Kang
AU - Stein, Dan J.
AU - Sussmann, Jess E.
AU - Temmingh, Henk S.
AU - Thompson, Paul M.
AU - Verdolini, Norma
N1 - Publisher Copyright:
© 2019, The Author(s), under exclusive licence to American College of Neuropsychopharmacology.
PY - 2019/12/1
Y1 - 2019/12/1
N2 - Fronto-limbic white matter (WM) abnormalities are assumed to lie at the heart of the pathophysiology of bipolar disorder (BD); however, diffusion tensor imaging (DTI) studies have reported heterogeneous results and it is not clear how the clinical heterogeneity is related to the observed differences. This study aimed to identify WM abnormalities that differentiate patients with BD from healthy controls (HC) in the largest DTI dataset of patients with BD to date, collected via the ENIGMA network. We gathered individual tensor-derived regional metrics from 26 cohorts leading to a sample size of N = 3033 (1482 BD and 1551 HC). Mean fractional anisotropy (FA) from 43 regions of interest (ROI) and average whole-brain FA were entered into univariate mega- and meta-analyses to differentiate patients with BD from HC. Mega-analysis revealed significantly lower FA in patients with BD compared with HC in 29 regions, with the highest effect sizes observed within the corpus callosum (R2 = 0.041, Pcorr < 0.001) and cingulum (right: R2 = 0.041, left: R2 = 0.040, Pcorr < 0.001). Lithium medication, later onset and short disease duration were related to higher FA along multiple ROIs. Results of the meta-analysis showed similar effects. We demonstrated widespread WM abnormalities in BD and highlighted that altered WM connectivity within the corpus callosum and the cingulum are strongly associated with BD. These brain abnormalities could represent a biomarker for use in the diagnosis of BD. Interactive three-dimensional visualization of the results is available at www.enigma-viewer.org.
AB - Fronto-limbic white matter (WM) abnormalities are assumed to lie at the heart of the pathophysiology of bipolar disorder (BD); however, diffusion tensor imaging (DTI) studies have reported heterogeneous results and it is not clear how the clinical heterogeneity is related to the observed differences. This study aimed to identify WM abnormalities that differentiate patients with BD from healthy controls (HC) in the largest DTI dataset of patients with BD to date, collected via the ENIGMA network. We gathered individual tensor-derived regional metrics from 26 cohorts leading to a sample size of N = 3033 (1482 BD and 1551 HC). Mean fractional anisotropy (FA) from 43 regions of interest (ROI) and average whole-brain FA were entered into univariate mega- and meta-analyses to differentiate patients with BD from HC. Mega-analysis revealed significantly lower FA in patients with BD compared with HC in 29 regions, with the highest effect sizes observed within the corpus callosum (R2 = 0.041, Pcorr < 0.001) and cingulum (right: R2 = 0.041, left: R2 = 0.040, Pcorr < 0.001). Lithium medication, later onset and short disease duration were related to higher FA along multiple ROIs. Results of the meta-analysis showed similar effects. We demonstrated widespread WM abnormalities in BD and highlighted that altered WM connectivity within the corpus callosum and the cingulum are strongly associated with BD. These brain abnormalities could represent a biomarker for use in the diagnosis of BD. Interactive three-dimensional visualization of the results is available at www.enigma-viewer.org.
UR - http://www.scopus.com/inward/record.url?scp=85071620394&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85071620394&partnerID=8YFLogxK
U2 - 10.1038/s41386-019-0485-6
DO - 10.1038/s41386-019-0485-6
M3 - Article
C2 - 31434102
AN - SCOPUS:85071620394
SN - 0893-133X
VL - 44
SP - 2285
EP - 2293
JO - Neuropsychopharmacology
JF - Neuropsychopharmacology
IS - 13
ER -