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维生素 D 缺乏对儿童和青少年精神科患者抑郁症状的影响 - 一项随机对照试验:研究方案。

Effect of an vitamin D deficiency on depressive symptoms in child and adolescent psychiatric patients - a randomized controlled trial: study protocol.

机构信息

Department of Child and Adolescent Psychiatry, University Hospital Essen, University of Duisburg-Essen, Wickenburgstr. 21, D-45147, Essen, Germany.

Pediatric Endocrinology and Diabetology, Kinderklinik II, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.

出版信息

BMC Psychiatry. 2018 Mar 1;18(1):57. doi: 10.1186/s12888-018-1637-7.

Abstract

BACKGROUND

Depression is a significant health and economic burden worldwide affecting not only adults but also children and adolescents. Current treatment options for this group are scarce and show moderate effect sizes. There is emerging evidence that dietary patterns and specific nutritional components might play a role in the risk for developing depression. This study protocol focusses on the role of vitamin D which is for long known to be relevant for calcium and phosphorous homeostasis and bone health but might also impact on mental health. However, the assessment of the vitamin D status of depressed juvenile patients, or supplementation of vitamin D is currently not part of routine treatment. Controlled intervention studies are indispensable to prove whether a vitamin D deficiency ameliorates depressive symptoms.

METHODS/DESIGN: This double blinded, randomized controlled trial will enroll 200 inpatients from a child and adolescent psychiatric department with a vitamin D deficiency defined by a 25(OH)-vitamin D-level < 30 nmol/l (12 ng/ml) and a Beck Depressions Inventory (BDI-II) score > 13 (indicating at least: mild depression). Upon referral, all patients will be screened, checked for inclusion criteria, and those eligible will be randomized after written consent into a supplementation or placebo group. Both study-arms will receive treatment-as-usual for their psychiatric disorder according to established clinical guidelines. The participants of the vitamin D supplementation group will receive 2640 I.E. vitamin D3 q.d. for 28 days in accordance with best practice in pediatric endocrinology. We hypothesize that delaying supplementation of vitamin D in the placebo arm will affect the treatment success of the depressive symptomatology in comparison to the vitamin D supplementation group. Patients will be enrolled for a period of 28 days based on the mean length of hospitalization of juveniles with depression.

DISCUSSION

Randomized controlled trials in children and adolescents with depression are needed to elucidate the role of a vitamin D deficiency for mental disorders and to investigate the relevance of a routine assessment and supplementation of vitamin D deficits.

TRIAL REGISTRATION

DRKS00009758, 16/06/2016 (retrospectively registered).

摘要

背景

抑郁症是一种全球性的重大健康和经济负担,不仅影响成年人,还影响儿童和青少年。目前针对这一群体的治疗选择有限,且效果中等。越来越多的证据表明,饮食模式和特定的营养成分可能在抑郁症的发病风险中起作用。本研究方案侧重于维生素 D 的作用,维生素 D 长期以来被认为与钙和磷的体内平衡以及骨骼健康有关,但也可能对心理健康产生影响。然而,评估抑郁青少年患者的维生素 D 状态或补充维生素 D 目前并不是常规治疗的一部分。对照干预研究对于证明维生素 D 缺乏是否可以改善抑郁症状是不可或缺的。

方法/设计:这项双盲、随机对照试验将招募 200 名来自儿童和青少年精神病科的住院患者,这些患者的维生素 D 缺乏症由 25(OH)-维生素 D 水平<30 nmol/L(12ng/ml)和贝克抑郁量表(BDI-II)评分>13(表示至少存在:轻度抑郁)定义。在转介时,所有患者将接受筛查,检查是否符合纳入标准,符合条件的患者将在书面同意后随机分为补充组或安慰剂组。根据既定的临床指南,两个研究组将根据其精神疾病接受常规治疗。维生素 D 补充组的参与者将根据儿科内分泌学的最佳实践,每天接受 2640 国际单位维生素 D3,持续 28 天。我们假设,与维生素 D 补充组相比,在安慰剂组中延迟补充维生素 D 会影响抑郁症状治疗的成功率。根据有抑郁症状的青少年的平均住院时间,患者将被招募 28 天。

讨论

需要在儿童和青少年抑郁症患者中进行随机对照试验,以阐明维生素 D 缺乏与精神障碍的关系,并研究常规评估和补充维生素 D 缺乏的相关性。

试验注册

DRKS00009758,2016 年 6 月 16 日(回顾性注册)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2113/5831612/353e35e4382c/12888_2018_1637_Fig1_HTML.jpg

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