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Genetic Association Studies of Suicidal Behavior: A Review of the Past 10?Years, Progress, Limitations, and Future Directions

机译:自杀行为的遗传关联研究:过去10年的回顾,进展,局限性和未来方向

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Suicidal behaviors (SBs), which range from suicidal ideation to suicide attempts and completed suicide, represent a fatal dimension of mental ill-health. The involvement of genetic risk factors in SB is supported by family, twin, and adoption studies. The aim of this paper is to review recent genetic association studies in SBs including (i) case–control studies, (ii) family-based association studies, and (iii) genome-wide association studies (GWAS). Various studies on genetic associations have tended to suggest that a number of genes [e.g., tryptophan hydroxylase, serotonin receptors and transporters, or brain-derived neurotrophic factors (BDNFs)] are linked to SBs, but these findings are not consistently supported by the results obtained. Although the candidate–gene approach is useful, it is hampered by the present state of knowledge concerning the pathophysiology of diseases. Interpretations of GWAS results are mostly hindered by a lack of annotation describing the functions of most variation throughout the genome. Association studies have addressed a wide range of single-nucleotide polymorphisms in numerous genes. We have included 104 such studies, of which 10 are family-based association studies and 11 are GWAS. Numerous meta-analyses of case–control studies have shown significant associations of SB with variants in the serotonin transporter gene (5-HTT or SLC6A4) and the tryptophan hydroxylase 1 gene (TPH1), but others report contradictory results. The gene encoding BDNF and its receptor (NTRK2) are also promising candidates. Only two of the GWAS showed any significant associations. Several pathways are mentioned in an attempt to understand the lack of reproducibility and the disappointing results. Consequently, we review and discuss here the following aspects: (i) sample characteristics and confounding factors; (ii) statistical limits; (iii) gene–gene interactions; (iv) gene, environment, and by time interactions; and (v) technological and theoretical limits.
机译:从自杀念头到自杀未遂,再到自杀未遂的自杀行为(SBs)代表着精神疾病的致命方面。家庭,双胞胎和收养研究支持遗传风险因素参与SB。本文的目的是回顾SB中最近的遗传关联研究,包括(i)病例对照研究,(ii)基于家庭的关联研究和(iii)全基因组关联研究(GWAS)。关于遗传关联的各种研究倾向于表明许多基因[例如,色氨酸羟化酶,5-羟色胺受体和转运蛋白或脑源性神经营养因子(BDNF)]与SB相关联,但结果并不能始终支持这些发现。获得。尽管候选基因方法是有用的,但是它被有关疾病病理生理学的当前知识所阻碍。缺少注释来描述整个基因组中大多数变异的功能,很大程度上阻碍了GWAS结果的解释。关联研究已解决了众多基因中的广泛单核苷酸多态性。我们纳入了104项此类研究,其中10项是基于家庭的协会研究,11项是GWAS。大量病例对照研究的荟萃分析表明,SB与血清素转运蛋白基因(5-HTT或SLC6A4)和色氨酸羟化酶1基因(TPH1)的变异存在显着关联,但其他报告的结果却相互矛盾。编码BDNF及其受体(NTRK2)的基因也是很有前途的候选基因。 GWAS中只有两个显示出任何重要的关联。为了理解可重复性的缺乏和令人失望的结果,提到了几种途径。因此,我们在这里回顾和讨论以下方面:(i)样本特征和混杂因素; (ii)统计限制; (iii)基因-基因相互作用; (iv)基因,环境和时间相互作用; (v)技术和理论极限。

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