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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.
Obsessive-compulsive symptoms (OCSs) do not increase psychosis risk in clinical high-risk individuals. However, OCSs are linked to a 15-fold increased psychosis risk in population-level studies.
Area of Science:
- Psychiatry
- Clinical Psychology
- Epidemiology
Background:
- Obsessive-compulsive symptoms (OCSs) share phenomenological overlap with psychosis.
- Previous research on OCSs and psychosis risk has primarily focused on clinical high-risk (CHR) cohorts.
- Sampling biases in CHR cohorts may misestimate the true risk of OCSs for developing psychosis.
Purpose of the Study:
- To systematically review and meta-analyze the risk of OCSs in developing psychosis.
- To assess this risk in both clinical high-risk (CHR) and population-level cohorts.
- To address potential sampling biases in previous reviews.
Main Methods:
- Systematic review and meta-analysis of 11 selected studies.
- Two separate meta-analyses were conducted: one for CHR cohorts and one for register-based (population-level) cohorts.
- Risk ratios (RR) were calculated to estimate the association between OCSs and psychosis development.
Main Results:
- In CHR cohorts, no significant difference in psychosis risk was found between individuals with and without OCSs (RR=0.99, P=0.95).
- In register-based cohorts, OCSs were associated with a 15-fold increase in psychosis risk (RR=15.01, P<.001).
- Significant heterogeneity was noted in the register-based cohort analysis (I²=85.1%).
Conclusions:
- OCSs may increase the risk of developing psychosis in population-level cohorts, but not in CHR cohorts.
- The discrepancy suggests shared underlying vulnerabilities for OCSs and psychosis that may be masked in CHR samples.
- Further research is needed, acknowledging limitations due to study numbers and heterogeneity in population-level data.
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