TY - JOUR
T1 - Does relapse contribute to treatment resistance? Antipsychotic response in first- vs. second-episode schizophrenia
AU - Takeuchi, Hiroyoshi
AU - Siu, Cynthia
AU - Remington, Gary
AU - Fervaha, Gagan
AU - Zipursky, Robert B.
AU - Foussias, George
AU - Agid, Ofer
N1 - Funding Information:
H.T. has received fellowship grants from the Canadian Institutes of Health Research (CIHR), Centre for Addiction and Mental Health (CAMH) Foundation, the Japanese Society of Clinical Neuropsy-chopharmacology, and Astellas Foundation for Research on Metabolic Disorders, speaker’s honoraria from Meiji-Seika Pharma, Mochida, Otsuka, Sumitomo Dainippon Pharma, and Yoshitomi Yakuhin, and manuscript fees from Sumitomo Dainippon Pharma. C.S. has received funding and consulting fees and research support from Sunovion, Pfizer, and Dainippon Sumitomo Pharma, Centre for Addiction and Mental Health (CAMH), Hong Kong Health and Medical Research Grant, and the Chinese University of Hong Kong. G.R. has received research support from Novartis and HLS. G.Fervaha has no competing interests to disclose. G.Foussias has served on advisory boards for Hoffman-La Roche and Takeda, and received speaker’s fees from Hoffman-La Roche, Lundbeck, and Novartis. R.B.Z. has received speaker’s honoraria and an educational grant from Janssen-Ortho (Johnson & Johnson). O.A. has received speaker’s honoraria from Janssen-Ortho (Johnson & Johnson), Lundbeck, Mylan Pharmaceuticals, HLS, and Novartis, and consultant fees from Janssen-Ortho (Johnson & Johnson), Lundbeck, Otsuka, and Sumitomo Dainippon Pharma, and research support from Boehringer Ingelheim, Neurocrine Biosciences, Janssen-Ortho (Johnson & Johnson), Otsuka, and Sunovion.
Publisher Copyright:
© 2018, American College of Neuropsychopharmacology.
PY - 2019/5/1
Y1 - 2019/5/1
N2 - Although some studies have suggested that relapse may be associated with antipsychotic treatment resistance in schizophrenia, the number and quality of studies is limited. The current analysis included patients with a diagnosis of first-episode schizophrenia or schizoaffective disorder who met the following criteria: (1) referral to the First-Episode Psychosis Program between 2003 and 2013; (2) treatment with an oral second-generation antipsychotic according to a standardized treatment algorithm; (3) positive symptom remission; (4) subsequent relapse (i.e., second episode) in association with non-adherence; and (5) reintroduction of antipsychotic treatment with the same agent used to achieve response in the first episode. The following outcomes were used as an index of antipsychotic treatment response: changes in the brief psychiatric rating scale (BPRS) total and positive symptom scores and number of patients who achieved positive symptom remission and 20 and 50% response. A total of 130 patients were included in the analyses. Although all patients took the same antipsychotic in both episodes, there were significant episode-by-time interactions for all outcomes of antipsychotic treatment response over 1 year in favor of the first episode compared to the second episode (50% response rate: 48.7 vs. 10.4% at week 7; 88.2 vs. 27.8% at week 27, respectively). Although antipsychotic doses in the second episode were significantly higher than those in the first episode, results remained unchanged after adjusting for antipsychotic dose. The present findings suggest that antipsychotic treatment response is reduced or delayed in the face of relapse following effective treatment of the first episode of schizophrenia.
AB - Although some studies have suggested that relapse may be associated with antipsychotic treatment resistance in schizophrenia, the number and quality of studies is limited. The current analysis included patients with a diagnosis of first-episode schizophrenia or schizoaffective disorder who met the following criteria: (1) referral to the First-Episode Psychosis Program between 2003 and 2013; (2) treatment with an oral second-generation antipsychotic according to a standardized treatment algorithm; (3) positive symptom remission; (4) subsequent relapse (i.e., second episode) in association with non-adherence; and (5) reintroduction of antipsychotic treatment with the same agent used to achieve response in the first episode. The following outcomes were used as an index of antipsychotic treatment response: changes in the brief psychiatric rating scale (BPRS) total and positive symptom scores and number of patients who achieved positive symptom remission and 20 and 50% response. A total of 130 patients were included in the analyses. Although all patients took the same antipsychotic in both episodes, there were significant episode-by-time interactions for all outcomes of antipsychotic treatment response over 1 year in favor of the first episode compared to the second episode (50% response rate: 48.7 vs. 10.4% at week 7; 88.2 vs. 27.8% at week 27, respectively). Although antipsychotic doses in the second episode were significantly higher than those in the first episode, results remained unchanged after adjusting for antipsychotic dose. The present findings suggest that antipsychotic treatment response is reduced or delayed in the face of relapse following effective treatment of the first episode of schizophrenia.
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U2 - 10.1038/s41386-018-0278-3
DO - 10.1038/s41386-018-0278-3
M3 - Article
C2 - 30514883
AN - SCOPUS:85058054718
SN - 0893-133X
VL - 44
SP - 1036
EP - 1042
JO - Neuropsychopharmacology
JF - Neuropsychopharmacology
IS - 6
ER -