Innovation Sciences and Technologies, University of Cagliari, Cagliari, Italy.
Eur Rev Med Pharmacol Sci. 2021 Sep;25(18):5701-5724. doi: 10.26355/eurrev_202109_26789.
Bipolar disorder (BD) is a severe disorder, and it is associated with an increased risk of mortality. About 25% of patients with BD have attempted and 11% have died by suicide. All these characteristics suggest that the disorders within the bipolar spectrum are a crucial public health problem. With the development of molecular genetics in recent decades, it was possible to more easily detect risk genes associated with this disorder. This study aimed at summarizing the findings of systematic reviews and meta-analyses on the topic and assessing the quality of the available evidence.
PubMed/Medline and Web of Science were searched to identify systematic reviews and meta-analyses published during 2013-2019. Standard methodology was applied to synthesize and assess the retrieved literature.
This systematic review identifies a number of potential risk genes associated with bipolar disorder whose mechanism of action has yet to be confirmed. They are divided into several groups: 1) a list of the most significant susceptibility genetic factors associated with BD; 2) the implication of the ZNF804A gene in BD; 3) the role of genes involved in calcium signaling in BD; 4) DNA methylation in BD; 5) BD and risk suicide genes; 6) susceptibility genes for early-onset BD; 7) candidate genes common to both BD and schizophrenia; 8) genes involved in cognitive status in BD cases; 9) genes involved in structural alteration in BD brain tissue; 10) genes involved in lithium response in BD.
Future research should concentrate on molecular mechanisms by which genetic variants play a major role in BD. Supplemental research is needed to replicate the applicable results.
双相情感障碍(BD)是一种严重的障碍,与死亡率增加有关。大约 25%的 BD 患者有过自杀企图,11%的患者自杀身亡。所有这些特征表明,双相谱系内的障碍是一个重要的公共卫生问题。近几十年来,随着分子遗传学的发展,更容易检测到与这种障碍相关的风险基因。本研究旨在总结 2013-2019 年期间关于该主题的系统评价和荟萃分析的研究结果,并评估现有证据的质量。
在 PubMed/Medline 和 Web of Science 上搜索 2013-2019 年发表的系统评价和荟萃分析。采用标准方法综合和评估检索文献。
本系统综述确定了一些与双相情感障碍相关的潜在风险基因,其作用机制尚未得到证实。它们分为几个组:1)与 BD 最相关的显著易感性遗传因素列表;2)ZNF804A 基因在 BD 中的作用;3)钙信号转导在 BD 中的作用;4)BD 中的 DNA 甲基化;5)BD 和自杀风险基因;6)BD 早发的易感基因;7)BD 和精神分裂症共同的候选基因;8)BD 病例认知状态相关的基因;9)BD 脑组织结构改变相关的基因;10)BD 中锂反应相关的基因。
未来的研究应集中在遗传变异通过何种分子机制在 BD 中起主要作用。需要进行补充研究以复制适用的结果。