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FI
7.048
2014 Neuropsychopharmacology
Multimodal Voxel-Based Meta-Analysis of White Matter Abnormalities in Obsessive-Compulsive Disorder.
Radua J, Grau M, van den Heuvel OA, de Schotten MT, Stein DJ, Canales-Rodríguez EJ, Catani M, Mataix-Cols D

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Abstract

White matter abnormalities have long been suspected in obsessive-compulsive disorder (OCD) but the available evidence has been inconsistent. We conducted the first multimodal meta-analysis of white matter volume (WMV) and fractional anisotropy (FA) studies in OCD. All voxel-wise studies comparing WMV or FA between patients with OCD and healthy controls in the PubMed, ScienceDirect, Google Scholar, Web of Knowledge and Scopus databases were retrieved. Manual searches were also conducted and authors were contacted soliciting additional data. Thirty-four datasets were identified, of which 22 met inclusion criteria (five of them unpublished; comprising 537 adult and pediatric patients with OCD and 575 matched healthy controls). Whenever possible, raw statistical parametric maps were also obtained from the authors. Peak and raw WMV and FA data were combined using novel multimodal meta-analytic methods implemented in effect-size signed differential mapping (ES-SDM). Patients with OCD showed widespread white matter abnormalities, but findings were particularly robust in the anterior midline tracts (crossing between anterior parts of cingulum bundle and body of corpus callosum), which showed both increased WMV and decreased FA, possibly suggesting an increase of fiber crossing in these regions. This finding was also observed when the analysis was limited to adult participants, and especially pronounced in samples with a higher proportion of medicated patients. Therefore, patients with OCD may have widespread white matter abnormalities, particularly evident in anterior midline tracts, though these changes might be, at least in part, attributable to the effects of therapeutic drugs.Neuropsychopharmacology accepted article preview online, 10 January 2014. doi:10.1038/npp.2014.5.
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