Continuous Dopamine D2 Receptor Blockade and Long-Term Outcome in First-Episode Schizophrenia

精神分裂症(面向对象编程) 封锁 期限(时间) 多巴胺 多巴胺受体D2 结果(博弈论) 医学 多巴胺受体 多巴胺受体D3 精神科 神经科学 心理学 内科学 受体 数理经济学 物理 量子力学 数学
作者
Jari Tiihonen,Antti Tanskanen,Marco Solmi,José M. Rubio,Christoph U. Correll,John M. Kane,Heidi Taipale
出处
期刊:American Journal of Psychiatry [American Psychiatric Association]
卷期号:: 00-00
标识
DOI:10.1176/appi.ajp.20240321
摘要

It is not known what proportion of patients experience relapse in first-episode schizophrenia despite continuous dopamine D2 receptor blockade and whether breakthrough psychosis is attributable to long-term use of D2-blocking antipsychotics. Using data from a Finnish nationwide cohort, the authors sought to test the hypothesis that the incidence of breakthrough psychosis is accelerated among previously relapse-free patients receiving continuous D2 antagonist treatment beyond 5 years. All persons age 45 years or younger with first-episode schizophrenia were identified from the nationwide registry of inpatient care for the years 1996-2014. The primary outcome was a severe relapse leading to hospitalization among those treated continuously with long-acting injectable (LAI) antipsychotics. The secondary outcome was the incidence rate ratio (IRR) of relapse during years 2-10, using year 1 as the reference. A total of 305 patients initiated ensured LAI use during the first 30 days of follow-up. Kaplan-Meier analysis showed that during the 10-year follow-up, their cumulative probability of relapse was 45% (95% CI=35-57). The annual relapse incidence per person-year decreased from 0.26 (95% CI=0.20-0.35) during the first year to 0.05 (95% CI=0.01-0.19) during the fifth year, corresponding to an IRR of 0.18 (95% CI=0.04-0.74). During years 6-10, only four relapses occurred during 128 person-years, corresponding to an IRR of 0.12 (95% CI=0.03-0.33) compared with year 1. About 40%-50% of patients with first-episode schizophrenia will relapse despite continuous D2 blockade, apparently due to non-dopaminergic elements of the pathophysiology of the illness, as the results show that long-term dopamine receptor blockade is not associated with an increased risk of breakthrough psychosis.
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