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. 2019 Aug;29(8):905-913.
doi: 10.1016/j.euroneuro.2019.06.006. Epub 2019 Jul 11.

A cross sectional study of impact and clinical risk factors of antipsychotic-induced OCD

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A cross sectional study of impact and clinical risk factors of antipsychotic-induced OCD

Marjan Biria et al. Eur Neuropsychopharmacol. 2019 Aug.

Abstract

A large proportion of schizophrenia patients treated with second generation antipsychotics will develop Obsessive Compulsive Disorder (OCD). However, there are few studies about the impact of this comorbidity and who is at higher risk. In this study of clozapine-treated patients, we aimed to determine the impact on outcome of clozapine-induced OCD, as well as the clinical and sociodemographic risk factors related to OCD-onset in clozapine patients. We had strict and novel inclusion criteria to minimise mis-identification of cases. The Obsessive-Compulsive Inventory-Revised (OCI-R) was used to divide 231 clozapine-treated patients into extreme cases of OCD (OCI ≥ 24 or checking subscale ≥6) versus non-OCD (OCI <15 and checking subscale <4). The Global Assessment of Functioning (GAF), short version of Warwick-Edinburgh Wellbeing scale and Clinical Global Impression for schizophrenia (CGI) scales were used to determine outcome. Socio-demographic information was used to identify the risk factors for OCD development. We found that schizophrenia patients with OCD symptoms had a significantly lower patient rated wellbeing scores (p < 0.001) only (no difference in clinician rated wellbeing scores), higher CGI positive (p < 0.01) and higher CGI depressive scores (p < 0.05). The only risk factors that reached significance level were higher treatment dose (p < 0.01) and younger paternal age at birth (p < 0.05). There is scope for future studies based on e.g. imaging and genetic studies to further investigate causality, and in improving clinician screening for OCD.

Keywords: Antipsychotic; Clozapine; Obsessive compulsive disorder; Schizophrenia.

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Figures

Fig. 1
Fig. 1
(A) Shows the average scores on different subsets of the Clinical Global Impression (CGI) scale. (B) Shows the average scores on the Global Assessment of Functioning (GAF) rated by clinicians and the Wellbeing scores rated by patients themselves. The Wellbeing scores are converted to percentages. The significance levels of p < 0.05, p < 0.01, and p < 0.001 are indicated with one, two and three stars respectively.

References

    1. Baytunca B., Kalyoncu T., Ozel I., Erermiş S., Kayahan B., Öngur D. Early onset schizophrenia associated with obsessive-compulsive disorder: clinical features and correlates. Clin. Neuropharmacol. 2017;40:243–245. - PubMed
    1. Brander G., Rydell M., Kuja-Halkola R., Fernández de la Cruz L., Lichtenstein P., Serlachius E., Rück C., Almqvist C., D'Onofrio B.M., Larsson H., Mataix-Cols D. Association of perinatal risk factors with obsessive-compulsive disorder: a population-based birth cohort, sibling control study. JAMA Psychiatry. 2016;73:1135–1144. - PubMed
    1. Brown J.E., Mezquida G., Fernandez-Egea E. Well-being in clozapine-treated schizophrenia patients: the significance of positive symptoms. Compr. Psychiatry. 2016;68:140–146. - PubMed
    1. Busner J., Targum S.D. The clinical global impressions scale: applying a research tool in clinical practice. Psychiatry. 2007;4:28–37. - PMC - PubMed
    1. Chudal R., Leivonen S., Rintala H., Hinkka-Yli-Salomäki S., Sourander A. Parental age and the risk of obsessive compulsive disorder and Tourette syndrome / chronic tic disorder in a nationwide population-based sample. J. Affect. Disord. 2017;223:101–105. - PubMed

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