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Omega-3 fatty acids for the treatment of depressive disorders in children and adolescents: a meta-analysis of randomized placebo-controlled trials

机译:ω-3脂肪酸用于治疗儿童和青少年的抑郁症:随机安慰剂对照试验的荟萃分析

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To investigate the efficacy and safety of omega-3 fatty acids (O3FA) in treating depressive disorders in children and adolescents. We conducted a comprehensive search in electronic databases and hand-searched articles included for relevant studies. We included randomized controlled trials which studied on O3FA for treatment of children and adolescents with depression. The standard mean differences (SMDs) and the odds ratios (ORs) with 95% confidence intervals (CIs) were estimated by a random-effects model. The primary outcomes were end-point depressive symptoms scores (efficacy) and all-cause discontinuation (safety). The secondary outcome of response rate was also assessed. Subgroup analyses were performed by age, severity of depression and dosage. Risk of bias assessment was performed based on the Jadad score and the Cochrane Collaboration's risk-of-bias method. A total of four studies with 153 participants were included. In terms of efficacy, there was no significant difference of end-point depressive symptoms scores between O3FA and placebo (SMD?=?-?0.12, 95% CI -?0.53 to 0.30, P?=?0.58; I2=?30%). In terms of safety, the all-cause discontinuation showed no statistical significance between O3FA and placebo (OR?=?1.3, 95% CI 0.58 to 2.93, P?=?0.53; I2=?0%). The response rate of O3FA was also not significant better than that of placebo (OR?=?1.57, 95% CI 0.26 to 9.39, P?=?0.62; I2=?71%). Besides, there were also no significant differences in those subgroup analyses outcomes. The risk of bias of included trials were not high. Only considering the limited evidence of O3FA in the acute treatment of major depressive disorder, it did not seem to offer a clear advantage for children and adolescents.
机译:探讨Omega-3脂肪酸(O3FA)治疗儿童和青少年抑郁症的疗效和安全性。我们在电子数据库中进行了全面的搜索,并包括相关研究的手动搜索文章。我们包括随机对照试验,研究O3FA,用于治疗儿童和青少年的抑郁症。通过随机效应模型估计标准平均差异(SMD)和具有95%置信区间(CIS)的差异比率(或者)。主要结果是终点抑郁症状评分(疗效)和全部导致停药(安全)。还评估了响应率的二次结果。亚组分析由年龄,抑郁和剂量严重性进行。基于Jadad评分和Cochrane协作的偏倚方法进行偏见评估风险。共有四项与153名参与者的研究。在疗效方面,O3FA和安慰剂之间的终点抑郁症状差异没有显着差异(SMD?=α- - ?0.12,95%CI - ?0.53至0.30,P?= 0.58; I2 = 30% )。在安全性方面,全源性停药在O3FA和安慰剂之间没有统计学意义(或?=?1.3,95%CI 0.58至2.93,P?0.53; I2 = 0%)。 O3Fa的响应率也没有优于安慰剂(或?=Δ1.57,95%CI 0.26至9.39,p≤0.62; i2 = 71%)。此外,这些亚组分析结果也没有显着差异。包括含量的偏见的风险不高。只考虑在重症抑郁症的急性治疗中O3FA的有限证据,它似乎没有为儿童和青少年提供明显的优势。

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