Thalmeier Andreas, Dickmann Martin, Giegling Ina, Schneider Barbara, M Hartmann Annette, Maurer Konrad, Schnabel Axel, Kauert Gerold, Möller Hans-Jürgen, Rujescu Dan
Department of Psychiatry, Ludwig Maximilians University, Munich, Germany.
Int J Neuropsychopharmacol. 2008 Mar;11(2):217-28. doi: 10.1017/S1461145707007894. Epub 2007 Jul 3.
The neurobiological basis of suicidal behaviour is multifactorial and complex. Several lines of evidence indicate that environmental factors as well as multiple genes and interactions of both are implicated in its aetiology. The aim of this study was to establish the transcriptomic expression profile of post-mortem brain tissue of suicide victims in order to identify new candidate genes and biological patterns for suicidal behaviour. Post-mortem orbitofrontal cortex tissue was derived from 11 suicide victims and 10 non-psychiatric controls carefully selected from a brain bank of over 150 brains, and the expression of more than 23000 messenger RNAs was assessed in this case-control study. Validation experiments were carried out using quantitative RT-PCR as an independent method. A classification of the differentially expressed genes according to their biological function and statistical analyses of the data were performed in order to identify biological pathways that are over-represented in the suicide group. In total, 124 transcripts demonstrated significant changes (fold changes > or = 1.3, p value < or = 0.01), with 59 showing under-, and 65 over-expression in the suicide group. The results could be validated for nine particularly interesting transcripts (CDCA7L, CDH12, EFEMP1, MLC1, PCDHB5, PTPRR, S100A13, SCN2B, and ZFP36). The pathway analysis showed that the Gene Ontology categories 'central nervous system development', 'homophilic cell adhesion', 'regulation of cell proliferation' and 'transmission of nerve impulse' were significantly enriched. The differentially expressed genes and significant biological processes might be involved in the pathophysiology of suicide and warrant further attention.
自杀行为的神经生物学基础是多因素且复杂的。多条证据表明,环境因素以及多个基因及其二者的相互作用都与自杀行为的病因学有关。本研究的目的是建立自杀受害者死后脑组织的转录组表达谱,以识别自杀行为的新候选基因和生物学模式。死后眶额皮质组织取自11名自杀受害者和10名非精神科对照者,这些对照者是从一个拥有超过150个大脑的脑库中精心挑选出来的,在这项病例对照研究中评估了超过23000种信使核糖核酸的表达。使用定量逆转录聚合酶链反应作为独立方法进行了验证实验。根据差异表达基因的生物学功能进行分类,并对数据进行统计分析,以识别在自杀组中过度富集的生物学途径。总共124个转录本表现出显著变化(倍数变化≥1.3,p值≤0.01),其中59个在自杀组中表现为低表达,65个表现为高表达。九种特别有趣的转录本(CDCA7L、CDH12、EFEMP1、MLC1、PCDHB5、PTPRR、S100A13、SCN2B和ZFP36)的结果可以得到验证。通路分析表明,基因本体类别“中枢神经系统发育”“嗜同性细胞黏附”“细胞增殖调控”和“神经冲动传递”显著富集。差异表达基因和重要生物学过程可能参与了自杀的病理生理学,值得进一步关注。