TY - JOUR
T1 - Volume of subcortical brain regions in social anxiety disorder
T2 - mega-analytic results from 37 samples in the ENIGMA-Anxiety Working Group
AU - Groenewold, Nynke A
AU - Bas-Hoogendam, Janna Marie
AU - Amod, Alyssa R
AU - Laansma, Max A
AU - Van Velzen, Laura S
AU - Aghajani, Moji
AU - Hilbert, Kevin
AU - Oh, Hyuntaek
AU - Salas, Ramiro
AU - Jackowski, Andrea P
AU - Pan, Pedro M
AU - Salum, Giovanni A
AU - Blair, James R
AU - Blair, Karina S
AU - Hirsch, Joy
AU - Pantazatos, Spiro P
AU - Schneier, Franklin R
AU - Talati, Ardesheer
AU - Roelofs, Karin
AU - Volman, Inge
AU - Blanco-Hinojo, Laura
AU - Cardoner, Narcís
AU - Pujol, Jesus
AU - Beesdo-Baum, Katja
AU - Ching, Christopher R K
AU - Thomopoulos, Sophia I
AU - Jansen, Andreas
AU - Kircher, Tilo
AU - Krug, Axel
AU - Nenadić, Igor
AU - Stein, Frederike
AU - Dannlowski, Udo
AU - Grotegerd, Dominik
AU - Lemke, Hannah
AU - Meinert, Susanne
AU - Winter, Alexandra
AU - Erb, Michael
AU - Kreifelts, Benjamin
AU - Gong, Qiyong
AU - Lui, Su
AU - Zhu, Fei
AU - Mwangi, Benson
AU - Soares, Jair C
AU - Wu, Mon-Ju
AU - Bayram, Ali
AU - Canli, Mesut
AU - Tükel, Raşit
AU - Westenberg, P Michiel
AU - Heeren, Alexandre
AU - Cremers, Henk R
AU - ENIGMA consortium
N1 - © 2023. The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2023/3
Y1 - 2023/3
N2 - There is limited convergence in neuroimaging investigations into volumes of subcortical brain regions in social anxiety disorder (SAD). The inconsistent findings may arise from variations in methodological approaches across studies, including sample selection based on age and clinical characteristics. The ENIGMA-Anxiety Working Group initiated a global mega-analysis to determine whether differences in subcortical volumes can be detected in adults and adolescents with SAD relative to healthy controls. Volumetric data from 37 international samples with 1115 SAD patients and 2775 controls were obtained from ENIGMA-standardized protocols for image segmentation and quality assurance. Linear mixed-effects analyses were adjusted for comparisons across seven subcortical regions in each hemisphere using family-wise error (FWE)-correction. Mixed-effects d effect sizes were calculated. In the full sample, SAD patients showed smaller bilateral putamen volume than controls (left: d = -0.077, pFWE = 0.037; right: d = -0.104, pFWE = 0.001), and a significant interaction between SAD and age was found for the left putamen (r = -0.034, pFWE = 0.045). Smaller bilateral putamen volumes (left: d = -0.141, pFWE < 0.001; right: d = -0.158, pFWE < 0.001) and larger bilateral pallidum volumes (left: d = 0.129, pFWE = 0.006; right: d = 0.099, pFWE = 0.046) were detected in adult SAD patients relative to controls, but no volumetric differences were apparent in adolescent SAD patients relative to controls. Comorbid anxiety disorders and age of SAD onset were additional determinants of SAD-related volumetric differences in subcortical regions. To conclude, subtle volumetric alterations in subcortical regions in SAD were detected. Heterogeneity in age and clinical characteristics may partly explain inconsistencies in previous findings. The association between alterations in subcortical volumes and SAD illness progression deserves further investigation, especially from adolescence into adulthood.
AB - There is limited convergence in neuroimaging investigations into volumes of subcortical brain regions in social anxiety disorder (SAD). The inconsistent findings may arise from variations in methodological approaches across studies, including sample selection based on age and clinical characteristics. The ENIGMA-Anxiety Working Group initiated a global mega-analysis to determine whether differences in subcortical volumes can be detected in adults and adolescents with SAD relative to healthy controls. Volumetric data from 37 international samples with 1115 SAD patients and 2775 controls were obtained from ENIGMA-standardized protocols for image segmentation and quality assurance. Linear mixed-effects analyses were adjusted for comparisons across seven subcortical regions in each hemisphere using family-wise error (FWE)-correction. Mixed-effects d effect sizes were calculated. In the full sample, SAD patients showed smaller bilateral putamen volume than controls (left: d = -0.077, pFWE = 0.037; right: d = -0.104, pFWE = 0.001), and a significant interaction between SAD and age was found for the left putamen (r = -0.034, pFWE = 0.045). Smaller bilateral putamen volumes (left: d = -0.141, pFWE < 0.001; right: d = -0.158, pFWE < 0.001) and larger bilateral pallidum volumes (left: d = 0.129, pFWE = 0.006; right: d = 0.099, pFWE = 0.046) were detected in adult SAD patients relative to controls, but no volumetric differences were apparent in adolescent SAD patients relative to controls. Comorbid anxiety disorders and age of SAD onset were additional determinants of SAD-related volumetric differences in subcortical regions. To conclude, subtle volumetric alterations in subcortical regions in SAD were detected. Heterogeneity in age and clinical characteristics may partly explain inconsistencies in previous findings. The association between alterations in subcortical volumes and SAD illness progression deserves further investigation, especially from adolescence into adulthood.
KW - Adolescent
KW - Adult
KW - Anxiety
KW - Brain
KW - Humans
KW - Magnetic Resonance Imaging/methods
KW - Neuroimaging/methods
KW - Phobia, Social
UR - http://www.scopus.com/inward/record.url?scp=85146389629&partnerID=8YFLogxK
U2 - 10.1038/s41380-022-01933-9
DO - 10.1038/s41380-022-01933-9
M3 - Journal article
C2 - 36653677
SN - 1359-4184
VL - 28
SP - 1079
EP - 1089
JO - Molecular Psychiatry
JF - Molecular Psychiatry
IS - 3
ER -