A systematic review and meta-analysis of deep brain stimulation in treatment-resistant depression.
A systematic review and meta-analysis of deep brain stimulation in treatment-resistant depression.
复制标题
对难治性抑郁症的深部脑刺激的系统回顾和荟萃分析。
DOI:
10.1016/j.pnpbp.2017.11.012
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发表时间:
2018
影响因子:
5.6
通讯作者:
Xie Peng
中科院分区:
文献类型:
--
作者:
Zhou Chanjuan;Zhang Hanping;Qin Yinhua;Tian Tian;Xu Bing;Chen Jianjun;Zhou Xinyu;Zeng Li;Fang Liang;Qi Xunzhong;Lian Bin;Wang Haiyang;Hu Zicheng;Xie Peng
BackgroundDeep brain stimulation (DBS) has been applied in treatment-resistant depression (TRD) as a putative intervention targeting different brain regions. However, the antidepressant effects of DBS for TRD in recent clinical trials remain controversial.MethodsWe searched Scopus, EMBASE, the Cochrane Library, PubMed, and PsycINFO for all published studies investigating the efficacy of DBS in TRD up to Feb 2017. Hamilton depression rating scale (HDRS) scores and Montgomery–Asberg depression rating scale (MARDS) scores were compared between baseline levels and those after DBS using the standardized mean difference (SMD) with 95% confidence intervals (CIs). The pooled response and remission rates were described using Risk Difference with 95% CIs.ResultsWe identified 14 studies of DBS in TRD targeting the subcallosal cingulate gyrus (SCG), ventral capsule/ventral striatum (VC/VS), medial forebrain bundle (MFB), and nucleus accumbens (NAcc). The overall effect sizes showed a significant reduction in HDRS after DBS stimulation in these four regions, with a standardized mean difference of − 3.02 (95% CI = − 4.28 to − 1.77,p< 0.00001) for SCG, − 1.64 (95% CI = − 2.80 to − 0.49,p= 0.005) for VC/VS, − 2.43 (95% CI = − 3.66 to − 1.19,p= 0.0001) for MFB, and − 1.30 (95% CI = − 2.16 to − 0.44,p= 0.003) for NAcc. DBS was effective, with high response rates at 1, 3, 6, and 12 months. Some adverse events (AEs), especially some specific AEs related to targeting regions, occurred during the DBS treatment.ConclusionsDBS significantly alleviates depressive symptoms in TRD patients by targeting the SCG, VC/VS, MFB, and NAcc. Several adverse events might occur during DBS therapy, although it is uncertain whether some AEs can be linked to DBS treatment. Further confirmatory trials are required involving larger sample sizes.