Schmidt Ulrike, Keck Martin E, Buell Dominik R
Max Planck Institute of Psychiatry, Department of Clinical Research, Kraepelinstrasse 10, 80804 München, Germany.
Max Planck Institute of Psychiatry, Department of Clinical Research, Kraepelinstrasse 10, 80804 München, Germany; Clienia Privatklinik Schloessli, Schloesslistr. 8, CH-8618 Oetwil am See, Switzerland.
J Psychiatr Res. 2015 Jun;65:1-8. doi: 10.1016/j.jpsychires.2015.03.014. Epub 2015 Mar 24.
In the last couple of years, non-coding (nc) RNAs like micro-RNAs (miRNAs), small interference RNAs (siRNAs) and long ncRNAs (lncRNAs) have emerged as promising candidates for biomarkers and drug-targets in a variety of psychiatric disorders. In contrast to reports on ncRNAs in affective disorders, schizophrenia and anxiety disorders, manuscripts on ncRNAs in posttraumatic stress disorder (PTSD) and associated animal models are scarce. Aiming to stimulate ncRNA research in PTSD and to identify the hitherto most promising ncRNA candidates and associated pathways for psychotrauma research, we conducted the first review on ncRNAs in PTSD. We aimed to identify studies reporting on the expression, function and regulation of ncRNAs in PTSD patients and in animals exhibiting a PTSD-like syndrome. Following the PRISMA guidelines for systematic reviews, we systematically screened the PubMed database for clinical and animal studies on ncRNAs in PTSD, animal models for PTSD and animal models employing a classical fear conditioning paradigm. Using 112 different combinations of search terms, we retrieved 523 articles of which we finally included and evaluated three clinical and 12 animal studies. In addition, using the web-based tool DIANA miRPath v2.0, we searched for molecular pathways shared by the predicted targets of the here-evaluated miRNA candidates. Our findings suggest that mir-132, which has been found to be regulated in three of the here included studies, as well as miRNAs with an already established role in Alzheimer's disease (AD) seem to be particularly promising candidates for future miRNA studies in PTSD. These results are limited by the low number of human trials and by the heterogeneity of included animal studies.
在过去几年中,诸如微小RNA(miRNA)、小干扰RNA(siRNA)和长链非编码RNA(lncRNA)等非编码(nc)RNA已成为多种精神疾病生物标志物和药物靶点的有前景的候选者。与关于情感障碍、精神分裂症和焦虑症中ncRNA的报道相比,关于创伤后应激障碍(PTSD)及相关动物模型中ncRNA的文献很少。为了促进PTSD中ncRNA的研究,并确定迄今为止最有前景的ncRNA候选者以及心理创伤研究的相关途径,我们对PTSD中的ncRNA进行了首次综述。我们旨在确定报告PTSD患者以及表现出PTSD样综合征的动物中ncRNA的表达、功能和调控的研究。遵循系统评价的PRISMA指南,我们系统地在PubMed数据库中筛选了关于PTSD中ncRNA的临床和动物研究、PTSD动物模型以及采用经典恐惧条件范式的动物模型。使用112种不同的搜索词组合,我们检索到523篇文章,最终纳入并评估了3项临床研究和12项动物研究。此外,我们使用基于网络的工具DIANA miRPath v2.0,搜索了此处评估的miRNA候选者预测靶点共有的分子途径。我们的研究结果表明,在本文纳入的三项研究中发现其受到调控的mir-132,以及在阿尔茨海默病(AD)中已确立作用的miRNA,似乎是未来PTSD中miRNA研究特别有前景的候选者。这些结果受到人体试验数量少以及纳入动物研究的异质性的限制。