Department of Psychiatry, University Hospital Münster, University of Münster, Münster, Germany.
Discipline of Psychiatry, Adelaide Medical School, University of Adelaide, Adelaide, South Australia, Australia.
J Neurochem. 2024 Sep;168(9):1817-1825. doi: 10.1111/jnc.15946. Epub 2023 Aug 27.
Low-grade inflammation is considered as a pathophysiological mechanism in a subtype of patients with major depressive disorder (MDD). Anti-inflammatory drugs have shown efficacy in treating MDD. However, it remains unclear how to identify suitable patients for anti-inflammatory treatment of depression. This study investigates the predictive value of pre-treatment high-sensitivity C-Reactive Protein (hsCRP) stratification on the outcome of celecoxib augmentation of vortioxetine. The PREDDICT study was conducted as a randomized, double-blind, placebo-controlled 6-week trial on augmentation of vortioxetine with celecoxib between December 2017 and April 2020 at the University of Adelaide (Australia). The present analysis focusses on the question of whether the pre-treatment hsCRP measurement and stratification of patients to depression with inflammation (hsCRP >3 mg/L) or without inflammation (hsCRP ≤3 mg/L) has an impact on the outcome of anti-inflammatory treatment with celecoxib. A total of n = 119 mostly treatment-resistant MDD patients with moderate to severe symptomatology were recruited in the trial. There was no effect of treatment group (celecoxib or placebo), pre-treatment hsCRP strata (with/without inflammation), or interaction between the two terms on treatment outcome. The results of the current analysis do not support the hypothesis that pre-treatment hsCRP level is predictive for response to anti-inflammatory treatment with celecoxib in MDD patients. Further research is needed to identify appropriate biomarkers for the prediction of anti-inflammatory treatment outcome in depression. CLINICAL TRIALS REGISTRATION: Australian New Zealand Clinical Trials Registry (ANZCTR), ACTRN12617000527369p. Registered on 11 April 2017, http://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?ACTRN=12617000527369p.
低度炎症被认为是一种主要抑郁障碍(MDD)患者亚类的病理生理机制。抗炎药物已显示出治疗 MDD 的疗效。然而,目前尚不清楚如何确定适合抗炎治疗抑郁症的患者。本研究旨在探讨治疗前高敏 C 反应蛋白(hsCRP)分层对维拉唑酮增效塞来昔布治疗结局的预测价值。该研究 PREDDICT 是一项于 2017 年 12 月至 2020 年 4 月在阿德莱德大学(澳大利亚)进行的、针对维拉唑酮增效塞来昔布的随机、双盲、安慰剂对照 6 周试验。本分析主要关注以下问题:即治疗前 hsCRP 测量值以及将患者分为炎症(hsCRP >3mg/L)或无炎症(hsCRP ≤3mg/L)亚组是否会影响塞来昔布抗炎治疗的结局。该试验共纳入了 119 名大多为治疗抵抗性 MDD 患者,这些患者的症状中度至重度。治疗组(塞来昔布或安慰剂)、治疗前 hsCRP 分层(有/无炎症)或两者之间的相互作用均对治疗结局无影响。目前分析的结果不支持 hsCRP 水平可预测 MDD 患者塞来昔布抗炎治疗反应的假设。需要进一步研究以确定适当的生物标志物来预测抗抑郁治疗的结果。临床试验注册:澳大利亚新西兰临床试验注册中心(ANZCTR),ACTRN12617000527369p。于 2017 年 4 月 11 日注册,http://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?ACTRN=12617000527369p。