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Despite the availability of effective treatments for obsessive-compulsive disorder (OCD), a considerable proportion of patients still remain resistant to or lack access to treatment. These patients are more severely symptomatic, have poorer long-term functional outcomes, and may incur significant costs. Previous studies suggest that more severe OCD symptoms are associated with poorer cognitive functioning. To determine whether this association extends to more naturalistic settings, this study explored whether severity of obsessive-compulsive symptoms and related functional impairment in a clinical outpatient sample were associated with poorer cognitive functioning. Participants (N=119) completed self-report measures of OCD severity and related functional impairment, as well as the Cognitive Triad (Eysenck, Anderson, and Cloninger). Two levels of severity were defined by the number of symptoms endorsed for each obsessive-compulsive symptom. Functional impairment was measured by reporting work and social impairment associated with these symptoms, and functional impairment related to these symptoms and the associated work and social impairment was aggregated to create a composite measure. Poor cognitive functioning was defined by Z scores below the 10th percentile of the cognitive triad. Across levels of OCD symptom severity, higher rates of obsessive-compulsive symptoms were associated with poorer cognitive functioning. However, symptom-related impairment and composite functional impairment were associated with poorer cognitive functioning, even when symptom-related impairment was controlled. These findings suggest that, in a clinical sample of OCD patients, impairment in different cognitive domains is associated with presence of OCD symptoms. Interventions aimed at improving functional impairment are likely to be particularly beneficial for patients with greater levels of OCD symptoms.Main menu

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The synthesis of 11C- and 18F-labeled N-substituted analogues of cis-5-dihydro-4-(5-methyl-1,2,4-oxadiazol-3-yl)imidazol-2-thion-1-one (WAY-100635) is described, and the biodistribution of these compounds was evaluated in baboons. The compounds were prepared using a propargylation reaction, to minimize side reaction of the thiol group. High specific activity (ca. 21 Ci/mol) and good radiochemical yield were achieved. The biodistribution data indicated that a N-substituted WAY-100635 derivative, with high cerebral selectivity and binding in the 5-HT(1A) receptors, was suitable for PET studies.I was just thinking about that thing earlier… I never use the -devel branch, even when I have access to it, because it’s too buggy and has been for a while. But I have

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