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However, such abnormalities have additionally been reported in other psychiatric conditions, and until recently there has been few large\u2010scale investigations to compare such findings. The current study uses the Enhancing Neuroimaging Genetics through Meta\u2010Analysis (ENIGMA) consortium method of standardising structural brain measures to quantify case\u2013control differences and to compare brain\u2010correlates of substance use disorders with those published in relation to other psychiatric disorders. Using the ENIGMA protocols, we report effect sizes derived from a meta\u2010analysis of alcohol (seven studies, <jats:italic>N<\/jats:italic>\u00a0=\u2009798, 54% are cases) and cannabis (seven studies, <jats:italic>N<\/jats:italic>\u00a0=\u2009447, 45% are cases) dependent cases and age\u2010 and sex\u2010matched controls. We conduct linear analyses using harmonised methods to process and parcellate brain data identical to those reported in the literature for ENIGMA case\u2013control studies of major depression disorder (MDD), schizophrenia (SCZ) and bipolar disorder so that effect sizes are optimally comparable across disorders. R elationships between substance use disorder diagnosis and subcortical grey matter volumes and cortical thickness were assessed with intracranial volume, age and sex as co\u2010variates . After correcting for multiple comparisons, AUD case\u2013control meta\u2010analysis of subcortical regions indicated significant differences in the thalamus, hippocampus, amygdala and accumbens, with effect sizes (0.23) generally equivalent to, or larger than |0.23| those previously reported for other psychiatric disorders (except for the pallidum and putamen). On measures of cortical thickness, AUD was associated with significant differences bilaterally in the fusiform gyrus, inferior temporal gyrus, temporal pole, superior frontal gyrus, and rostral and caudal anterior cingulate gyri. Meta\u2010analysis of CUD case\u2013control studies indicated reliable reductions in amygdala, accumbens and hippocampus volumes, with the former effect size comparable to, and the latter effect size around half of that reported for alcohol and SCZ. CUD was associated with lower cortical thickness in the frontal regions, particularly the medial orbitofrontal region, but this effect was not significant after correcting for multiple testing. This study allowed for an unbiased cross\u2010disorder comparison of brain correlates of substance use disorders and showed alcohol\u2010related brain anomalies equivalent in effect size to that found in SCZ in several subcortical and cortical regions and significantly greater alterations than those found in MDD in several subcortical and cortical regions. Although modest, CUD results overlapped with findings reported for AUD and other psychiatric conditions, but appear to be most robustly related to reduce thickness of the medial orbitofrontal cortex.<\/jats:p>","DOI":"10.1002\/hbm.25114","type":"journal-article","created":{"date-parts":[[2020,7,9]],"date-time":"2020-07-09T11:04:53Z","timestamp":1594292693000},"page":"399-413","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":47,"title":["How do substance use disorders compare to other psychiatric conditions on structural brain abnormalities? 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