Higher orexin-A levels are associated with treatment response to clozapine in patients with schizophrenia: A cross-sectional study

Author:

Chen Po-Yu123,Chiu Chih-Chiang12,Chang Chin-Kuo456,Lu Mong-Liang278ORCID,Huang Cho-Yin1,Chen Chun-Hsin278,Huang Ming-Chyi1289ORCID

Affiliation:

1. Department of Psychiatry, Taipei City Psychiatric Center, Taipei City Hospital, Taipei, Taiwan

2. Department of Psychiatry, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan

3. Department of Psychology, National Chengchi University, Taipei, Taiwan

4. Global Health Program, College of Public Health, National Taiwan University, Taipei, Taiwan

5. Institute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University, Taipei, Taiwan

6. Department of Psychological Medicine, Institute of Psychiatry, Psychology & Neuroscience, King’s College London, London, UK

7. Department of Psychiatry, Wan Fang Hospital, Taipei Medical University, Taipei, Taiwan

8. Psychiatric Research Center, Wang-Fang Hospital, Taipei Medical University, Taipei, Taiwan

9. Psychiatric Research Center, Taipei Medical University Hospital, Taipei, Taiwan

Abstract

Background: Clozapine is the primary antipsychotic (APD) for treatment-resistant schizophrenia (TRS). However, only 40% of patients with TRS respond to clozapine, constituting a subgroup of clozapine-resistant patients. Recently, the neuropeptide orexin-A was shown to be involved in the pathophysiology of schizophrenia. This study evaluated the association of orexin-A levels with the clozapine response in patients with TRS. Methods: We recruited 199 patients with schizophrenia, including 37 APD-free and 162 clozapine-treated patients. Clozapine-treated patients were divided into clozapine-responsive ( n = 100) and clozapine-resistant ( n = 62) groups based on whether they had achieved psychotic remission defined by the 18-item Brief Psychiatric Rating Scale (BPRS-18). We compared blood orexin-A levels among the three groups and performed regression analysis to determine the association of orexin-A level with treatment response in clozapine-treated patients. We also explored the correlation between orexin-A levels and cognitive function, assessed using the CogState Schizophrenia Battery. Results: Clozapine-responsive patients had higher orexin-A levels than clozapine-resistant and APD-free patients. Orexin-A level was the only factor significantly associated with treatment response after adjustment. Orexin-A levels were negatively correlated with BPRS-18 full scale and positive, negative, and general symptoms subscale scores. We also observed a positive correlation between orexin-A levels and verbal memory, visual learning and memory, and working memory function. Conclusions: This cross-sectional study showed that higher levels of orexin-A are associated with treatment response to clozapine in patients with TRS. Future prospective studies examining changes in orexin-A level following clozapine treatment and the potential benefit of augmenting orexin-A signaling are warranted.

Funder

Taipei Institute of Pathology

Taipei City Government

Taipei City Hospital

National Science Council

Publisher

SAGE Publications

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