Abstract
BACKGROUND: Although it has been suggested that the hippocampus and amygdala (HA) are involved in the neurobiology of obsessive-compulsive disorder (OCD), volumetric findings have been inconsistent, and little work has been undertaken on the volumetry of the heterogeneous anatomic units of HA, with their specific functions and cytoarchitecture, in OCD. We sought to explore potential sources of heterogeneity in brain volumes by performing a separate analysis for people with and without psychotropic medication use, as well as the association of subfield volumes with OCD symptom severity. METHODS: We segmented T1-weighted images from people with OCD and healthy controls in the OCD Brain Imaging Consortium to produce 12 hippocampal subfields and 9 amygdala subfields using Free-Surfer 6.0. We assessed between-group differences in subfield volume using a mixed-effects model adjusted for age and quadratic effects of age, sex, site, and whole HA volume. We also performed subgroup analyses to examine subfield volume in relation to comorbid anxiety and depression, medication status, and symptom severity. We corrected all analyses for multiple comparisons using the false discovery rate (FDR). RESULTS: We included images from 381 people with OCD and 338 healthy controls. These groups did not significantly differ in HA subfield volumes. However, medicated people with OCD had significantly smaller volumes in the hippocampal dentate gyrus (pFDR = 0.04, d = -0.26) and molecular layer (pFDR = 0.04, d = -0.29), and larger volumes in the lateral (pFDR = 0.049, d = 0.23) and basal (pFDR = 0.049, d = 0.25) amygdala subfields, than healthy controls. Unmedicated people with OCD had significantly smaller volumes in the hippocampal cornu ammonis sector 1 (pFDR = 0.02, d = -0.28) than controls. We did not detect associations between any subfield volume and OCD severity. LIMITATIONS: We used cross-sectional data, which limits the interpretation of our analysis. CONCLUSION: Differences in HA subfields between people with OCD and healthy controls are dependent on medication status, in line with previous work on other brain volumetric alterations in OCD. This emphasizes the importance of considering psychotropic medication in neuroimaging studies of OCD.
| Original language | English |
|---|---|
| Pages (from-to) | E170-E180 |
| Number of pages | 11 |
| Journal | Journal of psychiatry & neuroscience : JPN |
| Volume | 50 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - 27 May 2025 |
Bibliographical note
Publisher Copyright:© 2025 CMA Impact Inc.
Funding
Ziphozihle Ntwatwa was partially funded by a grant from the Carnegie Corporation of New York. This work was supported in part by the Oppenheimer Memorial Trust. Other sources of support include the National Research Foundation of South Africa to Christine Lochner; Dutch Organization for Scientific Research (nos. 912-02-050, 907-00-012, 940-37-018, and 916.86.038); Carlos III Health Institute (nos. PI09/01331, PI10/01753, PI10/01003, CP10/00604, and CIBER-CB06/03/0034); Agency for Administration of University and Research (no. 2009SGR1554); a Miguel Servet contract from the Carlos III Health Institute (no. CP10/00604) to Carles Soriano-Mas; a Wellcome Trust project grant (no. 064846) to David Mataix-Cols; a grant from the Foundation for the Support of Research in the State of São Paulo to Euripedes Miguel (FAPESP; no. 2005/55628-8); a FAPESP scholarship to Marcelo Hoexter (2005/04206-6); Brain Science Convergence Research Program (RS-2023-00266120) and the Basic Research Program of the Korea Brain Research Institute (no. 25-BR-05-05) to Minah Kim, funded by the Ministry of Science and Information and Communication Technologies; and a National Research Foundation of Korea grant funded by the Ministry of Education, Science, and Technology (no. 2012-0005150).
| Funders | Funder number |
|---|---|
| Ministry of Science and ICT, South Korea | |
| National Research Foundation of Korea | |
| Ernest Oppenheimer Memorial Trust | |
| Carnegie Corporation of New York | |
| Fundação de Amparo à Pesquisa do Estado de São Paulo | 2005/04206-6, 2005/55628-8 |
| Nederlandse Organisatie voor Wetenschappelijk Onderzoek | 940-37-018, 912-02-050, 916.86.038, 907-00-012 |
| Brain Science Convergence Research Program | RS-2023-00266120 |
| Instituto de Salud Carlos III | PI10/01003, PI09/01331, PI10/01753, CIBER-CB06/03/0034, CP10/00604 |
| Agency for Administration of University and Research | 2009SGR1554 |
| Korea Brain Research Institute | 25-BR-05-05 |
| Wellcome Trust | 064846 |
| Ministry of Education, Science and Technology | 2012-0005150 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
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