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抗炎症治疗对重性抑郁障碍或抑郁症状的疗效:临床试验的荟萃分析。

Efficacy of anti-inflammatory treatment on major depressive disorder or depressive symptoms: meta-analysis of clinical trials.

机构信息

Psychosis Research Unit, Aarhus University Hospital Psychiatry, Aarhus, Denmark.

Department of Clinical Medicine, Aarhus University Hospital, Aarhus, Denmark.

出版信息

Acta Psychiatr Scand. 2019 May;139(5):404-419. doi: 10.1111/acps.13016. Epub 2019 Mar 28.

DOI:10.1111/acps.13016
PMID:30834514
Abstract

BACKGROUND

No study has gathered evidence from all randomized clinical trials (RCTs) with anti-inflammatory drugs measuring antidepressant effects including a detailed assessment of side-effects and bias.

METHODS

We performed a systematic review identifying RCTs published prior to January 1, 2018, studying antidepressant treatment effects and side-effects of pharmacological anti-inflammatory intervention in adults with major depressive disorder (MDD) or depressive symptoms. Outcomes were depression scores after treatment, remission, response, and side-effects. Pooled standard mean differences (SMD) and risk ratios (RR) including 95% confidence intervals (95%-CI) were calculated.

RESULTS

We identified 36 RCTs, whereof 13 investigated NSAIDs (N = 4214), 9 cytokine inhibitors (N = 3345), seven statins (N = 1576), 3 minocycline (N = 151), 2 pioglitazone (N = 77), and 2 glucocorticoids (N = 59). Anti-inflammatory agents improved depressive symptoms compared to placebo as add-on in patients with MDD (SMD = -0.64; 95%-CI = -0.88, -0.40; I  = 51%; N = 597) and as monotherapy (SMD = -0.41; 95%-CI = -0.60, -0.22; I  = 93%, N = 8825). Anti-inflammatory add-on improved response (RR = 1.76; 95%-CI = 1.44-2.16; I  = 16%; N = 341) and remission (RR = 2.14; 95%-CI = 1.03-4.48; I  = 57%; N = 270). We found a trend toward an increased risk for infections, and all studies showed high risk of bias.

CONCLUSION

Anti-inflammatory agents improved antidepressant treatment effects. Future RCTs need to include longer follow-up, identify optimal doses and subgroups of patients that can benefit from anti-inflammatory intervention.

摘要

背景

尚无研究从所有评估抗炎药物抗抑郁效果的随机临床试验(RCT)中收集证据,包括对副作用和偏倚的详细评估。

方法

我们进行了一项系统评价,以确定在 2018 年 1 月 1 日之前发表的 RCT,研究了在患有重度抑郁症(MDD)或抑郁症状的成年人中,药理学抗炎干预的抗抑郁治疗效果和副作用。结局是治疗后抑郁评分、缓解、反应和副作用。计算了汇总后的标准均数差(SMD)和风险比(RR),包括 95%置信区间(95%-CI)。

结果

我们确定了 36 项 RCT,其中 13 项研究了 NSAIDs(N=4214),9 项研究了细胞因子抑制剂(N=3345),7 项研究了他汀类药物(N=1576),3 项研究了米诺环素(N=151),2 项研究了吡格列酮(N=77),2 项研究了糖皮质激素(N=59)。抗炎药物作为 MDD 患者的附加治疗(SMD=-0.64;95%-CI=-0.88,-0.40;I=51%;N=597)和单药治疗(SMD=-0.41;95%-CI=-0.60,-0.22;I=93%;N=8825)均能改善抑郁症状。抗炎药物的附加治疗能改善反应(RR=1.76;95%-CI=1.44-2.16;I=16%;N=341)和缓解(RR=2.14;95%-CI=1.03-4.48;I=57%;N=270)。我们发现感染风险增加的趋势,而且所有研究均显示出高偏倚风险。

结论

抗炎药物改善了抗抑郁治疗效果。未来的 RCT 需要包括更长的随访时间,确定最佳剂量和可能受益于抗炎干预的患者亚组。

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