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Do Obsessive-Compulsive Symptoms Increase the Risk of Developing Psychosis? A Systematic Review and Meta-analysis
William Hinton1,2, Marco Vivolo1,2, Emma Jimenez1
1Department of Clinical Psychology and Psychological Therapies, Norwich Medical School, Faculty of Medicine and Health Sciences, University of East Anglia, Norwich Research Park, Norwich, Norfolk NR4 7TJ, United Kingdom.
Background And Hypothesis:
There is a phenomenological overlap of obsessive-compulsive symptoms (OCSs) and psychosis, leading to discussion about whether OCSs increase the risk of developing psychosis. Previous reviews have focused on clinical high-risk (CHR) cohorts, which may misestimate risk due to sampling biases. The current systematic review and meta-analyses aimed to determine the risk of OCSs on developing psychosis in individuals classified at CHR and at the population level.
Study Design:
A total of 2081 articles were screened, with 11 studies meeting the criteria for inclusion. Two separate meta-analyses were conducted for CHR cohorts and for register-based cohorts to estimate the risk ratio (RR) of OCSs for developing psychosis.
Study Results:
In CHR cohorts, the meta-analysis found no significant difference in the risk of developing psychosis between individuals with and without OCSs (RR = 0.99, 95% CI, 0.71-1.38, P = .95) across 8 studies with low heterogeneity (I 2 < 0.000%, 95% CI, 0-67.03). In register-based cohorts, OCSs were associated with a 15-fold increase in the risk of developing psychosis (RR = 15.01, 95% CI, 8.36-26.93, P < .001), although this estimate was derived from 3 studies with significant heterogeneity (I 2 = 85.1%, 95% CI, 37.14-99.67).
Conclusions:
The limited number of studies and high heterogeneity in the population-level cohort limit any firm conclusions. However, the findings indicate that OCSs may increase the risk of developing psychosis in the register-based cohorts, but not in CHR cohorts. The discrepancy may reflect shared underlying vulnerabilities present in both OCSs and psychosis that are obscured by samples enriched for psychosis risk.
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