The association between exposure to COX-2 inhibitors and schizophrenia deterioration. A nested case-control study

Pharmacopsychiatry. 2007 May;40(3):111-5. doi: 10.1055/s-2007-977714.

Abstract

Background: COX-2 inhibitors (COX-2i) have been reported to have beneficial effects on schizophrenia. This observational study assesses the association between exposure to COX-2i or/and NSAIDs and schizophrenia deterioration.

Methods: We conducted a case-control study within a cohort (n=3,485) of antipsychotic users with a schizophrenia diagnosis (ICD-9=295.x) in IMS-Lifelink, a US claims database. Case events indicating exacerbation of schizophrenia were: switching antipsychotic medication, starting combination therapy, using parenteral antipsychotics or an increasing dose. For each case one control was selected. Exposure to COX-2i/NSAIDs (current/recent/none) and cumulative exposure in Defined Daily Doses 90 days before the index/event date were assessed. Age, sex and co-medication were evaluated as confounders. Logistic regression analysis was used to assess the association.

Results: 1,443 case events occurred. For current use, no benefit on schizophrenia case events from exposure to COX-2i was found (adjusted OR 1.16; 95% CI 0.83-1.62). Instead, recent COX2i use with a duration of 0 to 93 days was associated with an increased risk for schizophrenia deterioration (adjusted OR 2.56; 95% CI 1.35-4.87). This association was strongest in rofecoxib. No relation was found for NSAIDs.

Conclusion: The use of COX-2i was not associated with a decreased risk for schizophrenia deterioration in this population.

Publication types

  • Comparative Study

MeSH terms

  • Age Factors
  • Anti-Inflammatory Agents, Non-Steroidal / adverse effects
  • Antipsychotic Agents / therapeutic use
  • Case-Control Studies
  • Cyclooxygenase 2 Inhibitors / adverse effects*
  • Female
  • Humans
  • Logistic Models
  • Male
  • Middle Aged
  • Schizophrenia / drug therapy
  • Schizophrenia / physiopathology*
  • Sex Factors
  • Time Factors

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Antipsychotic Agents
  • Cyclooxygenase 2 Inhibitors