Predicting treatment resistance in positive and negative symptom domains from first episode psychosis: Development of a clinical prediction model

IF 3.6 2区 医学 Q1 PSYCHIATRY Schizophrenia Research Pub Date : 2024-09-10 DOI:10.1016/j.schres.2024.09.010
{"title":"Predicting treatment resistance in positive and negative symptom domains from first episode psychosis: Development of a clinical prediction model","authors":"","doi":"10.1016/j.schres.2024.09.010","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>Treatment resistance (TR) in schizophrenia may be defined by the persistence of positive and/or negative symptoms despite adequate treatment. Whilst previous investigations have focused on positive symptoms, negative symptoms are highly prevalent, impactful, and difficult to treat. In the current study we aimed to develop easily employable prediction models to predict TR in positive and negative symptom domains from first episode psychosis (FEP).</p></div><div><h3>Methods</h3><p>Longitudinal cohort data from 1027 individuals with FEP was utilised. Using a robust definition of TR, <em>n</em> = 51 (4.97 %) participants were treatment resistant in the positive domain and <em>n</em> = 56 (5.46 %) treatment resistant in the negative domain 12 months after first presentation. 20 predictor variables, selected by existing evidence and availability in clinical practice, were entered into two LASSO regression models. We estimated the models using repeated nested cross-validation (NCV) and assessed performance using discrimination and calibration measures.</p></div><div><h3>Results</h3><p>The prediction model for TR in the positive domain showed good discrimination (AUC = 0.72). Twelve predictor variables (male gender, cannabis use, age, positive symptom severity, depression and academic and social functioning) were retained by each outer fold of the NCV procedure, indicating importance in prediction of the outcome. However, our negative domain model failed to discriminate those with and without TR, with results only just over chance (AUC = 0.56).</p></div><div><h3>Conclusions</h3><p>Treatment resistance of positive symptoms can be accurately predicted from FEP using routinely collected baseline data, however prediction of negative domain-TR remains a challenge. Detailed negative symptom domains, clinical data, and biomarkers should be considered in future longitudinal studies.</p></div>","PeriodicalId":21417,"journal":{"name":"Schizophrenia Research","volume":null,"pages":null},"PeriodicalIF":3.6000,"publicationDate":"2024-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0920996424004213/pdfft?md5=efb421067df4b03b9914361a7ac792ca&pid=1-s2.0-S0920996424004213-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Schizophrenia Research","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0920996424004213","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PSYCHIATRY","Score":null,"Total":0}
引用次数: 0

Abstract

Background

Treatment resistance (TR) in schizophrenia may be defined by the persistence of positive and/or negative symptoms despite adequate treatment. Whilst previous investigations have focused on positive symptoms, negative symptoms are highly prevalent, impactful, and difficult to treat. In the current study we aimed to develop easily employable prediction models to predict TR in positive and negative symptom domains from first episode psychosis (FEP).

Methods

Longitudinal cohort data from 1027 individuals with FEP was utilised. Using a robust definition of TR, n = 51 (4.97 %) participants were treatment resistant in the positive domain and n = 56 (5.46 %) treatment resistant in the negative domain 12 months after first presentation. 20 predictor variables, selected by existing evidence and availability in clinical practice, were entered into two LASSO regression models. We estimated the models using repeated nested cross-validation (NCV) and assessed performance using discrimination and calibration measures.

Results

The prediction model for TR in the positive domain showed good discrimination (AUC = 0.72). Twelve predictor variables (male gender, cannabis use, age, positive symptom severity, depression and academic and social functioning) were retained by each outer fold of the NCV procedure, indicating importance in prediction of the outcome. However, our negative domain model failed to discriminate those with and without TR, with results only just over chance (AUC = 0.56).

Conclusions

Treatment resistance of positive symptoms can be accurately predicted from FEP using routinely collected baseline data, however prediction of negative domain-TR remains a challenge. Detailed negative symptom domains, clinical data, and biomarkers should be considered in future longitudinal studies.

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
预测首次发病的精神病患者在阳性和阴性症状领域的治疗阻力:开发临床预测模型
背景精神分裂症的耐药性(TR)可定义为在接受充分治疗后仍持续出现阳性和/或阴性症状。以往的研究主要集中在阳性症状方面,而阴性症状的发病率高、影响大且难以治疗。在本研究中,我们旨在开发易于使用的预测模型,以预测首发精神病(FEP)患者在阳性和阴性症状领域的TR。采用可靠的TR定义,在首次发病12个月后,n = 51(4.97%)名参与者在阳性症状领域出现治疗耐药,n = 56(5.46%)名参与者在阴性症状领域出现治疗耐药。我们将根据现有证据和临床实践选择的 20 个预测变量输入两个 LASSO 回归模型。我们使用重复嵌套交叉验证(NCV)对模型进行了估计,并使用辨别度和校准度对模型的性能进行了评估。结果阳性领域 TR 的预测模型显示出良好的辨别度(AUC = 0.72)。12个预测变量(男性性别、吸食大麻、年龄、阳性症状严重程度、抑郁、学业和社会功能)在NCV程序的每个外层折叠中都被保留下来,这表明了预测结果的重要性。然而,我们的阴性领域模型却无法区分有和没有TR的患者,其结果仅略高于偶然性(AUC = 0.56)。结论利用常规收集的基线数据,可以从FEP中准确预测阳性症状的治疗耐受性,但阴性领域-TR的预测仍是一项挑战。未来的纵向研究应考虑详细的阴性症状域、临床数据和生物标志物。
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
Schizophrenia Research
Schizophrenia Research 医学-精神病学
CiteScore
7.50
自引率
8.90%
发文量
429
审稿时长
10.2 weeks
期刊介绍: As official journal of the Schizophrenia International Research Society (SIRS) Schizophrenia Research is THE journal of choice for international researchers and clinicians to share their work with the global schizophrenia research community. More than 6000 institutes have online or print (or both) access to this journal - the largest specialist journal in the field, with the largest readership! Schizophrenia Research''s time to first decision is as fast as 6 weeks and its publishing speed is as fast as 4 weeks until online publication (corrected proof/Article in Press) after acceptance and 14 weeks from acceptance until publication in a printed issue. The journal publishes novel papers that really contribute to understanding the biology and treatment of schizophrenic disorders; Schizophrenia Research brings together biological, clinical and psychological research in order to stimulate the synthesis of findings from all disciplines involved in improving patient outcomes in schizophrenia.
期刊最新文献
Schizophrenia and antipsychotic medications present distinct and shared gut microbial composition: A meta-analysis. Association of CACNA1C polymorphisms (rs1006737, rs4765905, rs2007044) with schizophrenia: A meta-analysis and trial sequential analysis. Aligning phenomenology and neuroscience of the basic and narrative self in schizophrenia. Dyadic interaction in schizophrenia - A promising new avenue of investigation? Early and later remission from clinical high risk of psychosis. A latent class and predictor analysis
×
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:481959085
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