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这些遗传关联数据对抑郁症患者自杀风险高有何说明?一种新的基于网络的方法,用于寻找抑郁症和自杀行为的共同分子基础以及相关治疗靶点。

What do the genetic association data say about the high risk of suicide in people with depression? A novel network-based approach to find common molecular basis for depression and suicidal behavior and related therapeutic targets.

机构信息

Department of Neuroscience, Faculty of Advanced Technologies in Medicine, Iran University of Medical Sciences (IUMS), Tehran, Iran.

Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences (TUMS), Tehran, Iran.

出版信息

J Affect Disord. 2018 Mar 15;229:463-468. doi: 10.1016/j.jad.2017.12.079. Epub 2018 Jan 8.

Abstract

BACKGROUND

Available sources indicate that the risk of suicide in people with major depression is higher than other psychiatric disorders. Although it seems that these two conditions may have a shared cause in some cases, no studies have been conducted to identify a common basis for them.

METHODS

In this study, following an extensive review of literature, we found almost all the genes that are involved in major depression and suicidal behavior, and we isolated genes shared between the two conditions. Then, we found all physical or functional interactions within three mentioned gene sets and reconstructed three genetic interactive networks. All networks were analyzed topologically and enriched functionally. Finally, using a drug repurposing approach, we found the main available drugs that interacted with the most central genes shared between suicidal behavior and depression.

RESULTS

The results demonstrated that BDNF, SLC6A4, CREB1, and TNF are the most fundamental shared genes; and generally, disordered dopaminergic, serotonergic, and immunologic pathways in neuronal projections are the main shared deficient pathways. In addition, we found two genes, SLC6A4 and SLC6A2, to be the main therapeutic targets, and Serotonin-Norepinephrine Reuptake Inhibitors (SNRI) and Tricyclic Antidepressants (TCA) to be the most effective drugs for individuals with depression at risk for suicide.

CONCLUSIONS

Our results, in addition to shedding light on the integrated molecular basis of depression-suicide, offer new therapeutic targets for individuals with depression at high risk for suicide and could pave the way for future preclinical and clinical studies. However, integrative systems biology-based studies highly depend on existing data and related databases, as well as the arrival of new experimental data sources in the future, possibly affecting the current results.

摘要

背景

现有资料表明,患有重度抑郁症的人群自杀风险高于其他精神障碍。尽管这两种情况在某些情况下可能具有共同的病因,但尚未有研究确定它们的共同基础。

方法

在这项研究中,我们在广泛查阅文献后,发现了几乎所有与重度抑郁症和自杀行为相关的基因,并分离出这两种情况共有的基因。然后,我们找到了这两组基因之间所有的物理或功能相互作用,并重建了三个遗传相互作用网络。对所有网络进行拓扑分析和功能富集分析。最后,我们采用药物重定位方法,找到了与自杀行为和抑郁症之间共享的最核心基因相互作用的主要现有药物。

结果

结果表明,BDNF、SLC6A4、CREB1 和 TNF 是最基本的共有基因;一般来说,神经元投射中多巴胺能、5-羟色胺能和免疫紊乱途径是主要的共有缺陷途径。此外,我们发现 SLC6A4 和 SLC6A2 这两个基因是主要的治疗靶点,而 5-羟色胺去甲肾上腺素再摄取抑制剂(SNRI)和三环类抗抑郁药(TCA)是对有自杀风险的抑郁症患者最有效的药物。

结论

我们的研究结果不仅阐明了抑郁-自杀的综合分子基础,还为有自杀风险的抑郁症患者提供了新的治疗靶点,并为未来的临床前和临床研究铺平了道路。然而,基于整合系统生物学的研究高度依赖于现有数据和相关数据库,以及未来新的实验数据源的出现,这可能会影响当前的结果。

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