학술논문

An overview of the first 5 years of the ENIGMA obsessive–compulsive disorder working group: The power of worldwide collaboration
Document Type
article
Source
Human Brain Mapping. 43(1)
Subject
Biological Psychology
Psychology
Brain Disorders
Clinical Research
Serious Mental Illness
Pediatric
Neurosciences
Mental Health
Mental health
Neurological
Cerebral Cortex
Humans
Machine Learning
Multicenter Studies as Topic
Neuroimaging
Obsessive-Compulsive Disorder
cortical thickness
ENIGMA
mega-analysis
meta-analysis
MRI
obsessive-compulsive disorder
surface area
volume
ENIGMA-OCD working group
Cognitive Sciences
Experimental Psychology
Biological psychology
Cognitive and computational psychology
Language
Abstract
Neuroimaging has played an important part in advancing our understanding of the neurobiology of obsessive-compulsive disorder (OCD). At the same time, neuroimaging studies of OCD have had notable limitations, including reliance on relatively small samples. International collaborative efforts to increase statistical power by combining samples from across sites have been bolstered by the ENIGMA consortium; this provides specific technical expertise for conducting multi-site analyses, as well as access to a collaborative community of neuroimaging scientists. In this article, we outline the background to, development of, and initial findings from ENIGMA's OCD working group, which currently consists of 47 samples from 34 institutes in 15 countries on 5 continents, with a total sample of 2,323 OCD patients and 2,325 healthy controls. Initial work has focused on studies of cortical thickness and subcortical volumes, structural connectivity, and brain lateralization in children, adolescents and adults with OCD, also including the study on the commonalities and distinctions across different neurodevelopment disorders. Additional work is ongoing, employing machine learning techniques. Findings to date have contributed to the development of neurobiological models of OCD, have provided an important model of global scientific collaboration, and have had a number of clinical implications. Importantly, our work has shed new light on questions about whether structural and functional alterations found in OCD reflect neurodevelopmental changes, effects of the disease process, or medication impacts. We conclude with a summary of ongoing work by ENIGMA-OCD, and a consideration of future directions for neuroimaging research on OCD within and beyond ENIGMA.