Abstract
Larger thalamic volume has been found in children with obsessive-compulsive disorder (OCD) and children with clinical-level symptoms within the general population. Particular thalamic subregions may drive these differences. The ENIGMA-OCD working group conducted mega- and meta-analyses to study thalamic subregional volume in OCD across the lifespan. Structural T1-weighted brain magnetic resonance imaging (MRI) scans from 2649 OCD patients and 2774 healthy controls across 29 sites (50 datasets) were processed using the FreeSurfer built-in ThalamicNuclei pipeline to extract five thalamic subregions. Volume measures were harmonized for site effects using ComBat before running separate multiple linear regression models for children, adolescents, and adults to estimate volumetric group differences. All analyses were pre-registered ( https://osf.io/73dvy ) and adjusted for age, sex and intracranial volume. Unmedicated pediatric OCD patients (<12 years) had larger lateral (d = 0.46), pulvinar (d = 0.33), ventral (d = 0.35) and whole thalamus (d = 0.40) volumes at unadjusted p-values <0.05. Adolescent patients showed no volumetric differences. Adult OCD patients compared with controls had smaller volumes across all subregions (anterior, lateral, pulvinar, medial, and ventral) and smaller whole thalamic volume (d = -0.15 to -0.07) after multiple comparisons correction, mostly driven by medicated patients and associated with symptom severity. The anterior thalamus was also significantly smaller in patients after adjusting for thalamus size. Our results suggest that OCD-related thalamic volume differences are global and not driven by particular subregions and that the direction of effects are driven by both age and medication status.
Original language | English |
---|---|
Article number | 70 |
Pages (from-to) | 70 |
Number of pages | 1 |
Journal | Translational psychiatry |
Volume | 12 |
Issue number | 1 |
DOIs | |
Publication status | Published - Dec 2022 |
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The thalamus and its subnuclei-a gateway to obsessive-compulsive disorder. / ENIGMA OCD Working Group.
In: Translational psychiatry, Vol. 12, No. 1, 70, 12.2022, p. 70.Research output: Contribution to journal › Article › Academic › peer-review
TY - JOUR
T1 - The thalamus and its subnuclei-a gateway to obsessive-compulsive disorder
AU - Weeland, Cees J.
AU - Kasprzak, Selina
AU - de Joode, Niels T.
AU - Abe, Yoshinari
AU - Alonso, Pino
AU - Ameis, Stephanie H.
AU - Anticevic, Alan
AU - Arnold, Paul D.
AU - Balachander, Srinivas
AU - Banaj, Nerisa
AU - Bargallo, Nuria
AU - Batistuzzo, Marcelo C.
AU - Benedetti, Francesco
AU - Beucke, Jan C.
AU - Bollettini, Irene
AU - Brecke, Vilde
AU - Brem, Silvia
AU - Cappi, Carolina
AU - Cheng, Yuqi
AU - Cho, Kang Ik K.
AU - Costa, Daniel L. C.
AU - Dallaspezia, Sara
AU - Denys, Damiaan
AU - Eng, Goi Khia
AU - Ferreira, S. nia
AU - Feusner, Jamie D.
AU - Fontaine, Martine
AU - Fouche, Jean-Paul
AU - Grazioplene, Rachael G.
AU - Gruner, Patricia
AU - He, Mengxin
AU - Hirano, Yoshiyuki
AU - Hoexter, Marcelo Q.
AU - Huyser, Chaim
AU - Hu, Hao
AU - Jaspers-Fayer, Fern
AU - Kathmann, Norbert
AU - Kaufmann, Christian
AU - Kim, Minah
AU - Koch, Kathrin
AU - Bin Kwak, Yoo
AU - Kwon, Jun Soo
AU - Lazaro, Luisa
AU - Li, Chiang-Shan R.
AU - Lochner, Christine
AU - Marsh, Rachel
AU - Martínez-Zalacaín, Ignacio
AU - Mataix-Cols, David
AU - Menchón, Jose M.
AU - Minnuzi, Luciano
AU - Moreira, Pedro Silva
AU - Morgado, Pedro
AU - Nakagawa, Akiko
AU - Nakamae, Takashi
AU - Narayanaswamy, Janardhanan C.
AU - Nurmi, Erika L.
AU - Ortiz, Ana E.
AU - Pariente, Jose C.
AU - Piacentini, John
AU - Picó-Pérez, Maria
AU - Piras, Fabrizio
AU - Piras, Federica
AU - Pittenger, Christopher
AU - Reddy, Y. C. Janardhan
AU - Rodriguez-Manrique, Daniela
AU - Sakai, Yuki
AU - Shimizu, Eiji
AU - Shivakumar, Venkataram
AU - Simpson, Helen Blair
AU - Soreni, Noam
AU - Soriano-Mas, Carles
AU - Sousa, Nuno
AU - Spalletta, Gianfranco
AU - Stern, Emily R.
AU - Stevens, Michael C.
AU - Stewart, S. Evelyn
AU - Szeszko, Philip R.
AU - Takahashi, Jumpei
AU - Tanamatis, Tais
AU - Tang, Jinsong
AU - Thorsen, Anders Lillevik
AU - Tolin, David
AU - van der Werf, Ysbrand D.
AU - van Marle, Hein
AU - van Wingen, Guido A.
AU - Vecchio, Daniela
AU - Venkatasubramanian, G.
AU - Walitza, Susanne
AU - Wang, Jicai
AU - Wang, Zhen
AU - Watanabe, Anri
AU - Wolters, Lidewij H.
AU - Xu, Xiufeng
AU - Yun, Je-Yeon
AU - Zhao, Qing
AU - White, Tonya
AU - Thompson, Paul M.
AU - ENIGMA OCD Working Group
AU - Stein, Dan J.
AU - van den Heuvel, Odile A.
AU - Vriend, Chris
N1 - Funding Information: The ENIGMA Obsessive-Compulsive Disorder Working Group gratefully acknowledges support from the NIH BD2K award U54 EB020403 (PI: P.M. Thompson) and Amsterdam Neuroscience (CIA-2019-03-A to O.A. van den Heuvel, Amsterdam Neuroscience Alliance Project to G.A. van Wingen). Supported by the Japan Society for the Promotion of Science (JSPS; KAKENHI Grants No. 18K15523 to Y. Abe, No. 19K03308 to Y. Hirano and A. Nakagawa, No. 16K04342 to A. Nakagawa); National Institute of Mental Health (NIMH; Grant no. 5R01MH116038 to A. Anticevic, No. R01MH085900 to J.D. Feusner, No. K23 MH115206 to P. Gruner, No. R01MH104648 and No. R21MH101441 to R. Marsh, No. R01MH085900 and No. R01MH081864 to J. O’Neill, No. 1R01MH081864 to J. Piacentini, No. K24 MH121571 to C. Pittenger, No. R01 MH074934, No. R21/R33MH107589 and No. R01MH111794 to E.R. Stern, No. R01 MH074934 to D. Tolin); the Alberta Innovates Translational Health Chair in Child and Youth Mental Health and the Ontario Brain Institute funding P.D. Arnold; Swiss National Science Foundation (Grant No. 320030_130237) and the Hartmann Müller Foundation (Grant No. 1460) to S. Brem; Fundação Faculdade de Medicina (Grant No. 86.768 to D.L.C. Costa); the Japan Agency for Medical Research and Development (AMED Brain/MINDS Beyond program Grant No. JP21dm0307002 to Y. Hirano, No. JP21dm0307008 to Y. Sakai); Michael Smith Foundation for Health Research to F. Jaspers-Fayer; the Deutsche Forschungsgemeinschaft (DFG; to D. Rodriguez-Manrique, Grant No. DFG 815/6-1 to N. Kathmann, No. KO 3744/11-1 to K. Koch); The Basic Science Research Program through the National Research Foundation of Korea (NRF) (Grant no. 2019R1A2B5B03100844 to J.S. Kwon); the Marató TV3 Foundation (Grant No. 01/2010 and No. 091710 to L. Lazaro); the National Research Foundation of South Africa to C. Lochner; the Portuguese Foundation for Science and Technology (Fundação para a Ciência e a Tecnologia; FCT; Project No. UIDB/50026/2020 and No. UIDP/50026/2020 to P. Morgado and N. Sousa); the ICVS Scientific Microscopy Platform, member of the national infrastructure PPBI - Portuguese Platform of Bioimaging (Grant No. PPBI-POCI-01-0145-FEDER-022122); the Norte Portugal Regional Operational Programme (NORTE 2020; Grant No. NORTE-01-0145-FEDER-000039 to P. Morgado and N. Sousa), under the PORTUGAL 2020 Partnership Agreement, through the European Regional Development Fund (ERDF); the FLAD Science Award Mental Health 2021 to P. Morgado and N. Sousa; the Government of India grants from the Department of Science and Technology (Grants No. SR/S0/HS/0016/2011 to Y.C. Janardhan Reddy, and DST INSPIRE faculty grant -IFA12-LSBM-26 to J.C. Narayanaswamy) and from the Department of Biotechnology (Grants No. BT/PR13334/Med/30/259/2009 to Y.C. Janardhan Reddy, and No. BT/06/IYBA/2012 to Dr. Janardhanan C. Narayanaswamy, and Accelerator Program for Discovery in Brain Disorders using Stem cells (ADBS), Grant No. BT/PR17316/MED/31/326/2015 to S. Balachander); the Italian Ministry of Health (Grant No. RC19-20-21 to Fabrizio Piras, No. RC18-19-20-21/A to G. Spalletta); the Wellcome Trust-DBT India Alliance (Grant No. 500236/Z/11/Z to G. Venkatasubramanian, Early Career Fellowship Grant No. IA/CPHE/18/1/503956 to. V. Shivakumar); the Carlos III Health Institute (Grant No. PI16/00889 and No. PI19/01171 to C. Soriano-Mas); the Departament de Salut, Generalitat de Catalunya (Grant No. PERIS SLT006/17/249 to C. Soriano-Mas); the Agència de Gestió d’Ajuts Universitaris i de Recerca (Grant No. 2017 SGR 1262 to C. Soriano-Mas); the International OCD Foundation to P.R. Szeszko; the Helse Vest Health Authority (Grant No. 911754 and No. 911880 to A.L. Thorsen); the Netherlands Organisation for Health Research and Development (ZonMw; VIDI Grant No. 91717306 to O.A. van den Heuvel, TOP Grant No. 91211021 to T. White); the South African Medical Research Council (SAMRC) to D.J. Stein; the Dutch Brain Foundation (Nederlandse Hersenstichting; Grant No. HA-2017-00227 to C. Vriend). Publisher Copyright: © 2022, The Author(s).
PY - 2022/12
Y1 - 2022/12
N2 - Larger thalamic volume has been found in children with obsessive-compulsive disorder (OCD) and children with clinical-level symptoms within the general population. Particular thalamic subregions may drive these differences. The ENIGMA-OCD working group conducted mega- and meta-analyses to study thalamic subregional volume in OCD across the lifespan. Structural T1-weighted brain magnetic resonance imaging (MRI) scans from 2649 OCD patients and 2774 healthy controls across 29 sites (50 datasets) were processed using the FreeSurfer built-in ThalamicNuclei pipeline to extract five thalamic subregions. Volume measures were harmonized for site effects using ComBat before running separate multiple linear regression models for children, adolescents, and adults to estimate volumetric group differences. All analyses were pre-registered ( https://osf.io/73dvy ) and adjusted for age, sex and intracranial volume. Unmedicated pediatric OCD patients (<12 years) had larger lateral (d = 0.46), pulvinar (d = 0.33), ventral (d = 0.35) and whole thalamus (d = 0.40) volumes at unadjusted p-values <0.05. Adolescent patients showed no volumetric differences. Adult OCD patients compared with controls had smaller volumes across all subregions (anterior, lateral, pulvinar, medial, and ventral) and smaller whole thalamic volume (d = -0.15 to -0.07) after multiple comparisons correction, mostly driven by medicated patients and associated with symptom severity. The anterior thalamus was also significantly smaller in patients after adjusting for thalamus size. Our results suggest that OCD-related thalamic volume differences are global and not driven by particular subregions and that the direction of effects are driven by both age and medication status.
AB - Larger thalamic volume has been found in children with obsessive-compulsive disorder (OCD) and children with clinical-level symptoms within the general population. Particular thalamic subregions may drive these differences. The ENIGMA-OCD working group conducted mega- and meta-analyses to study thalamic subregional volume in OCD across the lifespan. Structural T1-weighted brain magnetic resonance imaging (MRI) scans from 2649 OCD patients and 2774 healthy controls across 29 sites (50 datasets) were processed using the FreeSurfer built-in ThalamicNuclei pipeline to extract five thalamic subregions. Volume measures were harmonized for site effects using ComBat before running separate multiple linear regression models for children, adolescents, and adults to estimate volumetric group differences. All analyses were pre-registered ( https://osf.io/73dvy ) and adjusted for age, sex and intracranial volume. Unmedicated pediatric OCD patients (<12 years) had larger lateral (d = 0.46), pulvinar (d = 0.33), ventral (d = 0.35) and whole thalamus (d = 0.40) volumes at unadjusted p-values <0.05. Adolescent patients showed no volumetric differences. Adult OCD patients compared with controls had smaller volumes across all subregions (anterior, lateral, pulvinar, medial, and ventral) and smaller whole thalamic volume (d = -0.15 to -0.07) after multiple comparisons correction, mostly driven by medicated patients and associated with symptom severity. The anterior thalamus was also significantly smaller in patients after adjusting for thalamus size. Our results suggest that OCD-related thalamic volume differences are global and not driven by particular subregions and that the direction of effects are driven by both age and medication status.
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85125154377&origin=inward
UR - https://www.ncbi.nlm.nih.gov/pubmed/35190533
U2 - 10.1038/s41398-022-01823-2
DO - 10.1038/s41398-022-01823-2
M3 - Article
C2 - 35190533
SN - 2158-3188
VL - 12
SP - 70
JO - Translational psychiatry
JF - Translational psychiatry
IS - 1
M1 - 70
ER -