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Meta-Analysis
. 2019 Dec;44(13):2285-2293.
doi: 10.1038/s41386-019-0485-6. Epub 2019 Aug 21.

Widespread white matter microstructural abnormalities in bipolar disorder: evidence from mega- and meta-analyses across 3033 individuals

Pauline Favre  1   2 Melissa Pauling  3   4 Jacques Stout  3 Franz Hozer  3   4   5   6 Samuel Sarrazin  3   4   7   8 Christoph Abé  9 Martin Alda  10 Clara Alloza  11   12 Silvia Alonso-Lana  13   14 Ole A Andreassen  15   16 Bernhard T Baune  17   18 Francesco Benedetti  19   20 Geraldo F Busatto  21   22 Erick J Canales-Rodríguez  13 Xavier Caseras  23 Tiffany Moukbel Chaim-Avancini  21   22 Christopher R K Ching  24   25 Udo Dannlowski  18 Michael Deppe  26 Lisa T Eyler  27   28 Mar Fatjo-Vilas  13   14 Sonya F Foley  29 Dominik Grotegerd  18 Tomas Hajek  10 Unn K Haukvik  15   16 Fleur M Howells  30   31 Neda Jahanshad  24 Harald Kugel  32 Trine V Lagerberg  15   16 Stephen M Lawrie  33 Julia O Linke  34   35 Andrew McIntosh  33   36 Elisa M T Melloni  37 Philip B Mitchell  38   39 Mircea Polosan  40 Edith Pomarol-Clotet  13   14 Jonathan Repple  18 Gloria Roberts  38   39 Annerine Roos  41 Pedro G P Rosa  21   22 Raymond Salvador  14   29 Salvador Sarró  14   29 Peter R Schofield  42   43 Mauricio H Serpa  19   20 Kang Sim  44   45   46 Dan J Stein  41 Jess E Sussmann  33 Henk S Temmingh  30   47 Paul M Thompson  25 Norma Verdolini  13   14   48 Eduard Vieta  14   48 Michele Wessa  34 Heather C Whalley  34 Marcus V Zanetti  20   21   49 Marion Leboyer  3   50   51 Jean-François Mangin  3 Chantal Henry  52 Edouard Duchesnay  3 Josselin Houenou  3   4   50   51 ENIGMA Bipolar Disorder Working Group
Affiliations
Meta-Analysis

Widespread white matter microstructural abnormalities in bipolar disorder: evidence from mega- and meta-analyses across 3033 individuals

Pauline Favre et al. Neuropsychopharmacology. 2019 Dec.

Erratum in

  • Correction: Widespread white matter microstructural abnormalities in bipolar disorder: evidence from mega- and meta-analyses across 3033 individuals.
    Favre P, Pauling M, Stout J, Hozer F, Sarrazin S, Abé C, Alda M, Alloza C, Alonso-Lana S, Andreassen OA, Baune BT, Benedetti F, Busatto GF, Canales-Rodríguez EJ, Caseras X, Chaim-Avancini TM, Ching CRK, Dannlowski U, Deppe M, Eyler LT, Fatjo-Vilas M, Foley SF, Grotegerd D, Hajek T, Haukvik UK, Howells FM, Jahanshad N, Kugel H, Lagerberg TV, Lawrie SM, Linke JO, McIntosh A, Melloni EMT, Mitchell PB, Polosan M, Pomarol-Clotet E, Repple J, Roberts G, Roos A, Rosa PGP, Salvador R, Sarró S, Schofield PR, Serpa MH, Sim K, Stein DJ, Sussmann JE, Temmingh HS, Thompson PM, Verdolini N, Vieta E, Wessa M, Whalley HC, Zanetti MV, Leboyer M, Mangin JF, Henry C, Duchesnay E, Houenou J; ENIGMA Bipolar Disorder Working Group. Favre P, et al. Neuropsychopharmacology. 2019 Dec;44(13):2298. doi: 10.1038/s41386-019-0521-6. Neuropsychopharmacology. 2019. PMID: 31527792 Free PMC article.

Abstract

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.

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Figures

Fig. 1
Fig. 1
Results of the mega-analysis. a Effect sizes of fractional anisotropy (FA) differences between patients with bipolar disorder (BD) and healthy controls projected on the 43 white matter (WM) tracts analyzed. b R squared (effect size) with confidence interval, sorted in increasing order of magnitude, for the regions showing significant differences between bipolar patients and healthy controls
Fig. 2
Fig. 2
Results of the meta-analysis. a Effect sizes for fractional anisotropy (FA) differences between patients with bipolar disorder (BD) and healthy controls projected on the 43 white matter (WM) tracts analyzed. b Cohen’s d (effect size) sorted in increasing order of magnitude for significant differences between bipolar patients and healthy controls. Significant findings after Bonferroni correction are highlighted in blue. Error bars represent standard error

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