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Study on risk factors of extrapyramidal symptoms induced by antipsychotics and its correlation with symptoms of schizophrenia
  1. Jiajun Weng1,2,
  2. Yan Zhang1,2,
  3. Huafang Li1,2,
  4. Yifeng Shen1,2 and
  5. Wenjuan Yu1,2
  1. 1Drug Clinical Trial Institution, Shanghai Mental Health Center, Shanghai, China
  2. 2Psychiatry, Shanghai Mental Health Center, Shanghai, China
  1. Correspondence to Wenjuan Yu; wenjuanyu2004{at}163.com

Abstract

Background Extrapyramidal symptoms (EPS) are one of the most common and neglected side effects during the treatment of schizophrenia. The risk factors of EPS in Chinese patients with schizophrenia and its relationship with psychiatric symptoms and mood symptoms of schizophrenia remain unknown.

Aims The main objective of this study is to explore the risk factors of EPS caused by antipsychotics and the relationship between EPS and psychotic symptoms and mood symptoms of schizophrenia.

Method This study included 679 patients with schizophrenia who have met the diagnostic criteria of the Diagnostic and Statistical Manual of Mental Disorders-Fourth Edition. Patients were divided into the EPS group and the non-EPS group according to the scale rating criteria and whether the anticholinergics have been used. The differences between demographic data and characters of drug intake were compared between the two groups, and the risk factors of EPS were selected between those factors. Correlation analysis was performed on the severity of schizophrenia (Positive and Negative Symptoms Scale (PANSS), Calgary Depression Scale for Schizophrenia (CDSS) score) and EPS scale (Simpson-Angus Scale (SAS), Barnes Akathisia Rating Scale (BARS), Abnormal Involuntary Movement Scale (AIMS) score) in 679 patients. The differences between the PANSS subscale score and the CDSS score between the EPS group and the non-EPS group were compared.

Result Compared with the non-EPS group, the EPS group patients are older, and they have a longer duration since first prescribed antipsychotics. The EPS group patients have higher frequency of atypical antipsychotics polytherapy and typical and atypical antipsychotics polytherapy or combined treatments with mood stabilisers. Logistic regression analysis shows that antipsychotics with high D2 receptor antagonistic effect and illness duration are the risk factors of EPS. The SAS score was significantly correlated with PANSS negative score, PANSS general psychopathological score and PANSS total score. The BARS scale score was significantly correlated with PANSS positive score, PANSS general psychopathological score, PANSS total score and CDSS total score. The AIMS scale score was significantly correlated with PANSS negative score. Compared with the non-EPS group, the EPS group patients have significantly higher PANSS negative score, PANSS general psychopathological score, PANSS total score and CDSS total score.

Conclusion Antipsychotic drugs with high D2 receptor antagonism and disease duration are risk factors of EPS in Chinese patients with schizophrenia. The severity of various types of EPS is significantly correlated with the psychiatric and mood symptoms of schizophrenia, and psychiatric symptoms and mood symptoms were significantly more severe in the EPS group. The occurrence of EPS is associated with poor treatment outcome of schizophrenia.

  • extrapyramidal symptoms
  • antipsychotics
  • schizophrenia

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Footnotes

  • Contributors WJ and YZ are responsible for the statistical analysis and the writing of the paper. HL is responsible for the scientific design of this study. YS and WY are responsible for the data checking and literature evaluation of this paper.

  • Funding Multicentre clinical study of Shanghai Jiao Tong University School of Medicine (DLY201620, 2016–2018): Real-world, multicentre clinical study of the long-term outcome of atypical antipsychotics in the treatment of schizophrenia 'Major new drug creation' Major science and technology project, National Major Project for IND, 2018ZX09734005 (2018–2020), Translational Medicine Collaborative Innovation Collaborative Research Project–Shanghai Mental Health Center Sub-center Construction (New Drug Clinical Trial Conversion Platform) (TM201624,2016–2018), Shanghai Science and Technology Commission Research Project (17411970300).

  • Competing interests None declared.

  • Patient consent for publication Obtained.

  • Ethics approval The Shanghai Mental Health Center Ethics Committee approved this study.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Data sharing statement No additional data are available.

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