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一项将米诺环素和/或ω-3脂肪酸添加到高危精神状态常规治疗中的随机、双盲、安慰剂对照试验(NAYAB):研究方案。

A randomised, double-blind, placebo-controlled trial of minocycline and/or omega-3 fatty acids added to treatment as usual for at-risk mental states (NAYAB): study protocol.

作者信息

Qurashi Inti, Chaudhry Imran B, Khoso Ameer B, Farooque Sana, Lane Steve, Husain Mohammad Omair, Chu Simon, Sarginson Jane, Hamarani Munir, Naqvi Haider A, Razzaque Bushra, Minhas Fareed A, Yung Alison R, Deakin J F W, Husain Nusrat

机构信息

Ashworth Research Centre, Mersey Care NHS Foundation Trust, Maghull, UK.

Faculty of Medicine, Biology and Health, University of Manchester, Manchester, UK.

出版信息

Trials. 2017 Nov 9;18(1):524. doi: 10.1186/s13063-017-2275-y.

Abstract

BACKGROUND

The at-risk mental state (ARMS) describes individuals at high risk of developing schizophrenia or psychosis. The use of antipsychotics in this population is not supported, because most individuals with ARMS are unlikely to develop psychosis. Anti-inflammatory treatments and polyunsaturated fatty acids (PUFAs) may have some beneficial effects in the treatment of ARMS. There have been no controlled clinical trials in which researchers have investigated the use of minocycline for ARMS and no trials involving PUFAs in combination with other proposed treatments. There is a need to find effective, tolerable and inexpensive interventions for individuals with ARMS that are available in high-, low- and middle-income countries.

METHODS/DESIGN: A 6-month intervention study of minocycline and/or omega-3 fatty acids added to treatment as usual (TAU) in patients with ARMS will be conducted in Pakistan using a randomised, placebo-controlled, double-blind factorial design. A total of 320 consenting patients with capacity will be recruited from the community, general practitioner clinics and psychiatric units. Allowing for a 25% dropout rate, we will recruit 59 completing participants into each study arm, and in total 236 will complete the study. We will determine whether the addition of minocycline and/or omega-3 fatty acids to TAU attenuates the rate of transition from ARMS to first-episode psychosis and improves symptoms and/or level of functioning in ARMS. We will also investigate whether any candidate risk factors, such as negative symptoms, influence treatment response in the ARMS group. The primary efficacy endpoint is conversion to psychotic disorder at 12 months after study entry. Analysis will be done according to the intention to treat principle using analysis of variance, chi-square tests and adjusted ORs to assess between-group differences. Cox regression analysis will be used to evaluate potential between-group differences in time to onset of psychosis.

DISCUSSION

The outcomes of this trial will provide evidence of the potential benefits of minocycline and PUFAs in the treatment of ARMS. Both minocycline and PUFAs are inexpensive, are readily available in low-/middle-income countries such as Pakistan, and if proven, may be safe and effective for treating individuals with ARMS.

TRIAL REGISTRATION

ClinicalTrials.gov, NCT02569307 . Registered on 3 October 2015.

摘要

背景

高危精神状态(ARMS)描述的是有发展为精神分裂症或精神病高风险的个体。不支持在该人群中使用抗精神病药物,因为大多数处于ARMS状态的个体不太可能发展为精神病。抗炎治疗和多不饱和脂肪酸(PUFA)可能对ARMS的治疗有一些有益作用。尚无研究人员对米诺环素用于ARMS进行研究的对照临床试验,也没有关于PUFA与其他拟用治疗方法联合使用的试验。需要为中低收入和高收入国家中处于ARMS状态的个体找到有效、可耐受且廉价的干预措施。

方法/设计:将在巴基斯坦采用随机、安慰剂对照、双盲析因设计,对ARMS患者在常规治疗(TAU)基础上加用米诺环素和/或ω-3脂肪酸进行为期6个月的干预研究。将从社区、全科医生诊所和精神科病房招募总共320名有行为能力且同意参与的患者。考虑到25%的失访率,我们将为每个研究组招募59名完成研究的参与者,总共236名将完成研究。我们将确定在TAU基础上加用米诺环素和/或ω-3脂肪酸是否能降低从ARMS转变为首发精神病的发生率,并改善ARMS患者的症状和/或功能水平。我们还将研究是否有任何候选风险因素,如阴性症状,会影响ARMS组的治疗反应。主要疗效终点是研究入组后12个月时转变为精神障碍。将根据意向性分析原则,使用方差分析、卡方检验和校正后的比值比来评估组间差异。将使用Cox回归分析来评估组间在精神病发病时间方面的潜在差异。

讨论

该试验的结果将为米诺环素和PUFA在ARMS治疗中的潜在益处提供证据。米诺环素和PUFA都价格低廉,在巴基斯坦等中低收入国家很容易获得,如果得到证实,可能对治疗ARMS个体安全有效。

试验注册

ClinicalTrials.gov,NCT02569307。于2015年10月3日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b820/5679379/c43b19938307/13063_2017_2275_Fig1_HTML.jpg

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