Department of Psychosis Studies, King's College London, Institute of Psychiatry, Psychology and Neuroscience, 16 De Crespigny Park, London, SE5 8AF, UK.
South London and Maudsley NHS Foundation Trust, Denmark Hill, London, SE5 8AZ, UK.
Trials. 2020 Jan 6;21(1):14. doi: 10.1186/s13063-019-3758-9.
People experiencing their first episode of psychosis are often deficient in vitamin D. Observational studies have reported an association between low vitamin D concentrations and poorer subsequent health outcomes in psychosis. A vitamin D deficiency in neonates and children has been linked to a later increased risk of schizophrenia and psychotic-like experiences. This trial aims to examine the effect of high-dose vitamin D supplementation on outcomes in early psychosis. We hypothesise that vitamin D supplementation will be associated with better mental health outcomes.
METHODS/DESIGN: The DFEND study is a multicentre double-blind placebo-controlled parallel-group trial of vitamin D supplementation in people with early psychosis. Patients with an ICD-10 diagnosis of functional psychosis will be randomised in a 1:1 ratio to receive either 120,000 IU/month of vitamin D (cholecalciferol) or a matched placebo for 6 months. The primary outcome is the total Positive and Negative Syndrome Scale (PANSS) score at the 6-month follow-up for all patients. Secondary outcomes include assessment of mood (Calgary Depression Scale), general function (Global Assessment of Functioning), cardiovascular risk (body mass index, waist circumference, C-reactive protein, cholesterol and HbA1c) and vitamin D levels at the 6-month follow-up. Additionally, 3- and 6-month total PANSS scores will be analysed for those with inadequate vitamin D levels at the baseline.
The DFEND study is the first trial to examine whether vitamin D supplementation in early psychosis is associated with better mental health outcomes. The findings of this study may help to resolve the clinical equipoise regarding the benefits and cost-effectiveness of routine vitamin D supplementation in people with psychosis.
ISRCTN, ISRCTN12424842. Registered on 25 February 2015.
首次出现精神病症状的人群往往缺乏维生素 D。观察性研究报告称,维生素 D 浓度低与精神病患者后续健康状况较差之间存在关联。新生儿和儿童的维生素 D 缺乏与以后精神分裂症和类精神病体验风险增加有关。本试验旨在研究大剂量维生素 D 补充对早期精神病患者结局的影响。我们假设维生素 D 补充将与更好的心理健康结果相关。
方法/设计:DFEND 研究是一项针对早期精神病患者维生素 D 补充的多中心、双盲、安慰剂对照、平行组试验。具有功能性精神病 ICD-10 诊断的患者将以 1:1 的比例随机分为两组,分别接受 120,000IU/月的维生素 D(胆钙化醇)或匹配的安慰剂治疗 6 个月。主要结局是所有患者在 6 个月随访时的阳性和阴性综合征量表(PANSS)总分。次要结局包括在 6 个月随访时评估情绪(卡尔加里抑郁量表)、一般功能(总体功能评估)、心血管风险(体重指数、腰围、C 反应蛋白、胆固醇和 HbA1c)和维生素 D 水平。此外,还将分析基线时维生素 D 水平不足的患者在 3 个月和 6 个月时的总 PANSS 评分。
DFEND 研究是第一项研究维生素 D 补充在早期精神病中是否与更好的心理健康结果相关的试验。该研究的结果可能有助于解决有关在精神病患者中常规补充维生素 D 的益处和成本效益的临床均衡问题。
ISRCTN,ISRCTN12424842。于 2015 年 2 月 25 日注册。