Insight into susceptibility genes associated with bipolar disorder: a systematic review

被引:8
作者
Kalcev, G. [1 ]
Preti, A. [2 ]
Scano, A. [3 ]
Orru, G. [3 ]
Carta, M. G. [2 ]
机构
[1] Univ Cagliari, Innovat Sci & Technol, Cagliari, Italy
[2] Univ Cagliari, Dept Publ Hlth Clin & Mol Med, Cagliari, Italy
[3] Univ Cagliari, Dept Surg Sci, Cagliari, Italy
关键词
Bipolar disorder; Genes; Gene regions; Genome-wide association; Genomic mutations; Chromosome; GENOME-WIDE ASSOCIATION; WHITE-MATTER MICROSTRUCTURE; NEUROTROPHIC FACTOR; SUICIDAL-BEHAVIOR; DNA METHYLATION; PSYCHIATRIC-DISORDERS; EARLY-ONSET; COGNITIVE IMPAIRMENT; AFFECTIVE-ILLNESS; MAJOR DEPRESSION;
D O I
10.26355/eurrev_202109_26789
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
OBJECTIVE: 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. MATERIALS AND METHODS: 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. RESULTS: 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. CONCLUSIONS: 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.
引用
收藏
页码:5701 / 5724
页数:24
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