Neuropsychological functions as trait markers in OCD: A 10-year follow-up study
1OCD Clinical and Research Unit, Psychiatry Department, Hospital Universitari de Bellvitge, Barcelona, Spain.
Background:
The alterations in neuropsychological performance described in Obsessive-Compulsive Disorder (OCD) reflect dysfunctions of the neurobiological structures underlying the disorder. Cognitive functions are influenced by clinical variables and are considered a potential endophenotype of the disorder. Although OCD is a chronic illness, data regarding the course of cognitive impairment are scarce.
Methods:
The present study assessed 60 OCD patients and 30 healthy controls (HC). Both groups were followed for a period of 10.6 years (range 5-18 years). Neuropsychological performance was assessed with a battery measuring executive subcomponents and non-verbal memory at baseline and after follow-up, using repeated-measures mixed models. Several clinical variables were also assessed in the patient group.
Results:
At baseline, patients with OCD demonstrated significantly poorer performance on neuropsychological tests than HC. Overall, the patterns of specific executive processes (organizational strategies and working memory) and non-verbal memory remained unchanged during the follow-up period in both groups. A reduction in severity of depression and obsessive-compulsive symptomatology was observed at the end of follow-up in OCD patients. In the sample, female sex was associated with worse performance on certain executive functions, and age with greater impairment in non-verbal memory after a decade of follow-up.
Conclusions:
OCD patients showed significant impairments on neuropsychological tests compared to HC at baseline. After follow-up, both groups showed a similar decline in neuropsychological performance, with no significant differences. These findings suggest that cognitive deficits in OCD remain stable over time and may reflect trait-like characteristics, and that sex may differentially affect cognitive performance with aging.
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