Predictors of Treatment-Resistant and Clozapine-Resistant Schizophrenia: A 12-Year Follow-up Study of First-Episode Schizophrenia-Spectrum Disorders

Author:

Chan Sherry Kit Wa12ORCID,Chan Hei Yan Veronica1,Honer William G3,Bastiampillai Tarun4,Suen Yi Nam1ORCID,Yeung Wai Song5,Lam Ming6,Lee Wing King7,Ng Roger Man King8,Hui Christy Lai Ming1,Chang Wing Chung12,Lee Edwin Ho Ming1,Chen Eric Yu Hai12

Affiliation:

1. Department of Psychiatry, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR

2. The State Key Laboratory of Brain and Cognitive Sciences, The University of Hong Kong, Hong Kong SAR

3. Department of Psychiatry, The University of British Columbia, Vancouver, Canada

4. Department of Psychiatry, Monash University, Melbourne, Australia

5. Department of Psychiatry, Pamela Youde Nethersole Eastern Hospital, Hong Kong SAR

6. Department of Psychiatry, Castle Peak Hospital, Hong Kong SAR

7. Department of Psychiatry, Kwai Chung Hospital, Hong Kong SAR

8. Department of Psychiatry, Kowloon Hospital, Hong Kong SAR

Abstract

Abstract Studies on the long-term development and early predictors of treatment-resistant schizophrenia (TRS) and clozapine-resistant TRS (CR-TRS) in patients with first-episode schizophrenia-spectrum disorders (FES) are limited and have not considered the impact of early intervention services (EIS). This study aimed to explore the development of TRS and CR-TRS among patients with FES over 12 years of follow-up. Of the 1234 patients with FES, 15% developed TRS. A total of 450 patients with schizophrenia or schizoaffective disorder were included in a nested case-control study (157 TRS and 293 non-TRS). Younger age of onset, poorer premorbid social adjustment during adulthood, longer duration of first episode, a greater number of relapses, and a higher antipsychotic dose in the first 24 months were associated with earlier TRS. CR-TRS patients, constituting 25% of TRS patients, had a poorer premorbid social adjustment in late adolescence and longer delay before clozapine initiation compared with non-CR-TRS. CR-TRS had poorer clinical and functional outcomes at 12-year follow-up. However, TRS patients on clozapine had a lower mortality rate compared with non-TRS patients. EIS did not have a significant impact on the development of TRS, but patients in the EIS group had a shorter delay of clozapine initiation. Results suggested that neurodevelopmental factors, early clinical characteristics, and requirement for higher antipsychotic dose may be associated with TRS development, highlighting multiple pathways leading to this form of illness. Specific interventions including relapse prevention and early initiation of clozapine during the early course of illness may reduce the rate of TRS and improve patient outcomes.

Funder

Health and Medical Research Fund

Hong Kong

Publisher

Oxford University Press (OUP)

Subject

Psychiatry and Mental health

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