Inflammation‐stratified augmentation of vortioxetine with celecoxib: Results from a double‐blind, randomized, placebo‐controlled trial in major depressive disorder

塞来昔布 沃替西汀 安慰剂 双盲 重性抑郁障碍 随机对照试验 医学 炎症 内科学 精神科 病理 替代医学 扁桃形结构
作者
Erhan Kavakbasi,Emma Sampson,Natalie Mills,Hikaru Hori,Kathrin Schwarte,Christa Hohoff,Klaus Oliver Schubert,Scott Clark,Célia Fourrier,Bernhard T. Baune
出处
期刊:Journal of Neurochemistry [Wiley]
被引量:5
标识
DOI:10.1111/jnc.15946
摘要

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.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
是神完成签到 ,获得积分10
1秒前
wulanshu应助bingsu108采纳,获得10
2秒前
ellen完成签到,获得积分10
2秒前
杜梦婷发布了新的文献求助10
2秒前
馒头发布了新的文献求助10
2秒前
漂亮听双完成签到,获得积分10
2秒前
3秒前
yehhh发布了新的文献求助30
3秒前
3秒前
何先生完成签到,获得积分20
3秒前
ghq完成签到,获得积分10
4秒前
5秒前
5秒前
5秒前
6秒前
知了完成签到 ,获得积分10
6秒前
solitude发布了新的文献求助10
6秒前
小奶瓶_发布了新的文献求助10
6秒前
7秒前
bai发布了新的文献求助10
7秒前
科目三应助罗谦平采纳,获得10
7秒前
8秒前
脑洞疼应助TAO采纳,获得10
9秒前
ZHH发布了新的文献求助10
9秒前
10秒前
lovesf发布了新的文献求助10
10秒前
mmmmm完成签到,获得积分10
10秒前
高高诗柳完成签到 ,获得积分10
10秒前
传奇3应助杜梦婷采纳,获得10
11秒前
11秒前
yehhh完成签到,获得积分10
12秒前
笙箫剑客发布了新的文献求助10
12秒前
12秒前
陌路完成签到,获得积分10
12秒前
哈哈应助电池小能手采纳,获得20
12秒前
科研通AI2S应助研了个研采纳,获得10
12秒前
13秒前
14秒前
落后的语海完成签到,获得积分10
15秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
A Research Agenda for Law, Finance and the Environment 800
Development Across Adulthood 800
Chemistry and Physics of Carbon Volume 18 800
The Organometallic Chemistry of the Transition Metals 800
A Time to Mourn, A Time to Dance: The Expression of Grief and Joy in Israelite Religion 700
The formation of Australian attitudes towards China, 1918-1941 640
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6447562
求助须知:如何正确求助?哪些是违规求助? 8260751
关于积分的说明 17598540
捐赠科研通 5509287
什么是DOI,文献DOI怎么找? 2902445
邀请新用户注册赠送积分活动 1879446
关于科研通互助平台的介绍 1719953