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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Cortical thickness in obsessive compulsive disorder: multisite mega-analysis of 780 brain scans from six centres

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Fouche, Jean-Paul ; du Plessis, Stefan ; Hattingh, Coenie ; Roos, Annerine ; Lochner, Christine ; Soriano-Mas, Carles ; Sato, Joao R. ; Nakamae, Takashi ; Nishida, Seiji ; Kwon, Jun Soo ; Jung, Wi Hoon ; Mataix-Cols, David ; Hoexter, Marcelo Q. ; Alonso, Pino ; de Wit, Stella J. ; Veltman, Dick J. ; Stein, Dan J. ; van den Heuvel, Odile A. ; Consortium, OCD Brain Imaging
Total Authors: 19
Document type: Journal article
Source: BRITISH JOURNAL OF PSYCHIATRY; v. 210, n. 1, p. 67-74, JAN 2017.
Web of Science Citations: 28
Abstract

Background There is accumulating evidence for the role of fronto-striatal and associated circuits in obsessive -compulsive disorder (OCD) but limited and conflicting data on alterations in cortical thickness. Aims To investigate alterations in cortical thickness and subcortical volume in OCD. Method In total, 412 patients with OCD and 368 healthy adults underwent magnetic resonance imaging scans. Between group analysis of covariance of cortical thickness and subcortical volumes was performed and regression analyses undertaken. Results Significantly decreased cortical thickness was found in the OCD group compared with controls in the superior and inferior frontal, precentral, posterior cingulate, middle temporal, inferior parietal and precuneus gyri. There was also a group x age interaction in the parietal cortex, with increased thinning with age in the OCD group relative to controls. Conclusions Our findings are partially consistent with earlier work, suggesting that group differences in grey matter volume and cortical thickness could relate to the same underlying pathology of OCD. They partially support a frontostriatal model of OCD, but also suggest that limbic, temporal and parietal regions play a role in the pathophysiology of the disorder. The group x age interaction effects may be the result of altered neuroplasticity. Copyright and usage (C) The Royal College of Psychiatrists 2017. (AU)

FAPESP's process: 11/21357-9 - Research on neural circuits and biological markers involved in obsessive-compulsive disorder using behavioral paradigms of fear and anxiety
Grantee:Eurípedes Constantino Miguel Filho
Support Opportunities: Research Projects - Thematic Grants