Identifying dopamine supersensitivity through a randomized controlled study of switching to aripiprazole from other antipsychotic agents in patients with schizophrenia.

IF 4 3区 医学 Q2 PHARMACOLOGY & PHARMACY Therapeutic Advances in Psychopharmacology Pub Date : 2022-01-28 eCollection Date: 2022-01-01 DOI:10.1177/20451253211064396
Chia-Hao Ma, Hung-Yu Chan, Ming H Hsieh, Chen-Chung Liu, Chih-Min Liu, Hai-Gwo Hwu, Ching-Hua Kuo, Wei J Chen, Tzung-Jeng Hwang
{"title":"Identifying dopamine supersensitivity through a randomized controlled study of switching to aripiprazole from other antipsychotic agents in patients with schizophrenia.","authors":"Chia-Hao Ma,&nbsp;Hung-Yu Chan,&nbsp;Ming H Hsieh,&nbsp;Chen-Chung Liu,&nbsp;Chih-Min Liu,&nbsp;Hai-Gwo Hwu,&nbsp;Ching-Hua Kuo,&nbsp;Wei J Chen,&nbsp;Tzung-Jeng Hwang","doi":"10.1177/20451253211064396","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Aripiprazole has been reported to worsen psychotic symptoms when switching from other antipsychotics, possibly due to dopamine supersensitivity psychosis.</p><p><strong>Objective: </strong>This study aimed to explore the predictors and possible underlying mechanisms of aripiprazole-related psychotic exacerbation.</p><p><strong>Methods: </strong>We conducted an 8-week, open-label, randomized controlled study from October 2007 to September 2009, assigning patients with a primary diagnosis of schizophrenia or schizoaffective disorder to switch from other antipsychotics to aripiprazole with 2-week dual administration, and then to taper off the original agents in fast (n = 38, within 1 week) or slow (n = 41, within 4 weeks) strategies. Positive and Negative Syndrome Scale (PANSS) was examined at day 0, 7, 14, 28, 56. Aripiprazole-related exacerbation (ARE) was defined positive as a 2-point increase in delusion/hallucination dimension score within 28 days compared with baseline. Baseline demographic, clinical and intervention-related variables were compared between the ARE+ and ARE- groups.</p><p><strong>Results: </strong>Of the 79 randomized patients, 21 fulfilled the criteria of ARE+ , and 46 were classified as ARE-. Fourteen patients in the ARE+ group had worsening psychotic symptoms in the first and second weeks. Compared with the ARE- group, the ARE+ group had a higher baseline chlorpromazine equivalent dose (405.8 ± 225.8 mg vs 268.1 ± 165.4 mg, <i>p</i> = 0.007) and was associated with prescription of first-generation antipsychotics (<i>p</i> = 0.038).</p><p><strong>Conclusions: </strong>A higher dose of original antipsychotics and prescription of first-generation antipsychotics may be associated with a higher risk of ARE. The underlying mechanism might be covert dopamine supersensitivity psychosis. These findings may help to identify high-risk patients and guide appropriate treatment strategies.</p><p><strong>Trial registration: </strong>ClinicalTrials.gov, identifier: NCT00545467.</p>","PeriodicalId":23127,"journal":{"name":"Therapeutic Advances in Psychopharmacology","volume":" ","pages":"20451253211064396"},"PeriodicalIF":4.0000,"publicationDate":"2022-01-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/b6/2f/10.1177_20451253211064396.PMC8801645.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Therapeutic Advances in Psychopharmacology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1177/20451253211064396","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Aripiprazole has been reported to worsen psychotic symptoms when switching from other antipsychotics, possibly due to dopamine supersensitivity psychosis.

Objective: This study aimed to explore the predictors and possible underlying mechanisms of aripiprazole-related psychotic exacerbation.

Methods: We conducted an 8-week, open-label, randomized controlled study from October 2007 to September 2009, assigning patients with a primary diagnosis of schizophrenia or schizoaffective disorder to switch from other antipsychotics to aripiprazole with 2-week dual administration, and then to taper off the original agents in fast (n = 38, within 1 week) or slow (n = 41, within 4 weeks) strategies. Positive and Negative Syndrome Scale (PANSS) was examined at day 0, 7, 14, 28, 56. Aripiprazole-related exacerbation (ARE) was defined positive as a 2-point increase in delusion/hallucination dimension score within 28 days compared with baseline. Baseline demographic, clinical and intervention-related variables were compared between the ARE+ and ARE- groups.

Results: Of the 79 randomized patients, 21 fulfilled the criteria of ARE+ , and 46 were classified as ARE-. Fourteen patients in the ARE+ group had worsening psychotic symptoms in the first and second weeks. Compared with the ARE- group, the ARE+ group had a higher baseline chlorpromazine equivalent dose (405.8 ± 225.8 mg vs 268.1 ± 165.4 mg, p = 0.007) and was associated with prescription of first-generation antipsychotics (p = 0.038).

Conclusions: A higher dose of original antipsychotics and prescription of first-generation antipsychotics may be associated with a higher risk of ARE. The underlying mechanism might be covert dopamine supersensitivity psychosis. These findings may help to identify high-risk patients and guide appropriate treatment strategies.

Trial registration: ClinicalTrials.gov, identifier: NCT00545467.

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
通过一项随机对照研究确定精神分裂症患者从其他抗精神病药物切换到阿立哌唑的多巴胺超敏感性。
背景:有报道称阿立哌唑在从其他抗精神病药物转用后会加重精神病症状,可能是由于多巴胺超敏感性精神病。目的:探讨阿立哌唑相关精神病加重的预测因素及可能的潜在机制。方法:从2007年10月至2009年9月,我们进行了一项为期8周的开放标签随机对照研究,将初步诊断为精神分裂症或分裂情感性障碍的患者从其他抗精神病药物切换到阿立哌唑,为期2周的双重给药,然后以快速(n = 38,在1周内)或缓慢(n = 41,在4周内)的策略逐渐减少原药物。分别于第0、7、14、28、56天检测阳性和阴性综合征量表(PANSS)。阿立哌唑相关恶化(ARE)被定义为28天内妄想/幻觉维度评分较基线增加2分。比较ARE+组和ARE-组的基线人口学、临床和干预相关变量。结果:79例随机患者中,21例符合ARE+标准,46例为ARE-。ARE+组14例患者在第1周和第2周出现精神病症状加重。与ARE-组相比,ARE+组氯丙嗪基线等效剂量更高(405.8±225.8 mg vs 268.1±165.4 mg, p = 0.007),且与第一代抗精神病药物处方相关(p = 0.038)。结论:较高的原始抗精神病药物剂量和第一代抗精神病药物处方可能与较高的ARE风险相关。潜在的机制可能是隐性多巴胺超敏性精神病。这些发现可能有助于识别高危患者并指导适当的治疗策略。试验注册:ClinicalTrials.gov,标识符:NCT00545467。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
7.90
自引率
2.40%
发文量
35
审稿时长
10 weeks
期刊介绍: Therapeutic Advances in Psychopharmacology delivers the highest quality peer-reviewed articles, reviews, and scholarly comment on pioneering efforts and innovative studies across all areas of psychopharmacology. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in psychopharmacology, providing a forum in print and online for publishing the highest quality articles in this area.
期刊最新文献
Levels of aripiprazole in the blood with an injection of aripiprazole administered once every two months: a plain language summary of publication. Anhedonia nonresponse to short-term ketamine administration for treatment-resistant bipolar depression. Adjunctive treatment with evenamide, a glutamate modulator, is associated with clinically meaningful benefits in patients with treatment-resistant schizophrenia and inadequate response to antipsychotics: recent clinical findings from randomized trials. A description of antipsychotic prescribing patterns on the inpatient behavioral health setting: a multicenter cross-sectional analysis. Acute and persistent withdrawal syndromes following discontinuation of antidepressants in children and adolescents: a systematic review.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1