NIHR Leicester Biomedical Research Centre, Leicester General Hospital, College of Life Sciences, University of Leicester, Leicester LE5 4PW, UK.
Diabetes Research Centre, University Hospitals of Leicester NHS Trust, Leicester LE5 4PW, UK.
Nutrients. 2022 Apr 27;14(9):1827. doi: 10.3390/nu14091827.
Background: Omega-3 polyunsaturated fatty acids′ concurrent benefits for cardiometabolic and mental health are equivocal. Despite lack of evidence, up to a third of adults consume Omega-3 supplements. No review has yet been published to report effect on depression in this cardiometabolic population. Methods: We conducted a systematic review of double-blinded, controlled randomised trials to investigate the safety and effect of Omega-3 supplementation on depression scores in people with cardiometabolic diseases. Primary outcome was change in depression scores versus placebo. Secondary outcomes were side-effects, concurrent medication and adherence. Results: Seven trials reporting on 2575 (672 female) adults aged 39−73 were included. Omega-3 dosages ranged from 1−3 g with an intervention duration of 10−48 weeks. Six out of seven trials found no statistically or clinically significant change to depression scores compared to placebo. One trial favoured intervention (Relative Risk Reduction: 47.93%, 95% CI: 24.89−63.98%, p < 0.001). Sub-analyses showed clinically meaningful reductions in depression scores for those on antidepressants (Intervention: 20.9 (SD: 7.1), Placebo: 24.9 (SD: 8.5) p < 0.05) or with severe depression (−1.74; 95% CI −3.04 to −0.05, p < 0.05) in two separate trials. Side effects were comparable between treatment arms. Conclusions: Omega-3 supplementation is safe to use but not superior to placebo for depression in adults with concurrent cardiometabolic disease.
ω-3 多不饱和脂肪酸对心脏代谢和心理健康的有益作用尚不确定。尽管缺乏证据,但多达三分之一的成年人服用ω-3 补充剂。尚未有综述报道ω-3 补充剂对该心脏代谢人群的抑郁影响。
我们对双盲、对照随机试验进行了系统评价,以调查ω-3 补充剂对患有心脏代谢疾病的人群的抑郁评分的安全性和效果。主要结局是与安慰剂相比抑郁评分的变化。次要结局是副作用、同时服用的药物和依从性。
纳入了 7 项试验,共报告了 2575 名(672 名女性)年龄在 39-73 岁的成年人。ω-3 剂量范围为 1-3 克,干预时间为 10-48 周。7 项试验中有 6 项发现与安慰剂相比,抑郁评分没有统计学或临床意义上的变化。一项试验倾向于干预(相对风险降低:47.93%,95%CI:24.89-63.98%,p<0.001)。亚分析显示,对于服用抗抑郁药的患者(干预组:20.9(SD:7.1),安慰剂组:24.9(SD:8.5),p<0.05)或有严重抑郁的患者(-1.74;95%CI -3.04 至-0.05,p<0.05),抑郁评分有临床意义的降低,这是在两项单独的试验中得出的结果。治疗组之间的副作用相当。
ω-3 补充剂在患有心脏代谢合并症的成年人中使用安全,但在治疗抑郁方面并不优于安慰剂。