Janiri Delfina, Kotzalidis Georgios D, di Luzio Michelangelo, Giuseppin Giulia, Simonetti Alessio, Janiri Luigi, Sani Gabriele
Department of Neurology, Fondazione Policlinico Universitario Agostino Gemelli IRCCS.
Department of Psychiatry and Neurology, Sapienza University of Rome.
Psychiatr Genet. 2021 Apr 1;31(2):50-64. doi: 10.1097/YPG.0000000000000274.
There is evidence of genetic polymorphism influences on brain structure and function, genetic risk in bipolar disorder (BD), and neuroimaging correlates of BD. How genetic influences related to BD could be reflected on brain changes in BD has been efficiently reviewed in a 2017 systematic review. We aimed to confirm and extend these findings through a Preferred Reporting Items for Systematic reviews and Meta-Analyses-based systematic review. Our study allowed us to conclude that there is no replicated finding in the timeframe considered. We were also unable to further confirm prior results of the BDNF gene polymorphisms to affect brain structure and function in BD. The most consistent finding is an influence of the CACNA1C rs1006737 polymorphism in brain connectivity and grey matter structure and function. There was a tendency of undersized studies to obtain positive results and large, genome-wide polygenic risk studies to find negative results in BD. The neuroimaging genetics in BD field is rapidly expanding.
有证据表明基因多态性会影响大脑结构和功能、双相情感障碍(BD)的遗传风险以及BD的神经影像学关联。2017年的一项系统评价有效地综述了与BD相关的基因影响如何在BD的大脑变化中得到体现。我们旨在通过基于系统评价和Meta分析的首选报告项目进行系统评价来证实并扩展这些发现。我们的研究使我们得出结论,在所考虑的时间范围内没有重复的发现。我们也无法进一步证实BDNF基因多态性影响BD大脑结构和功能的先前结果。最一致的发现是CACNA1C rs1006737多态性对大脑连通性以及灰质结构和功能的影响。在BD研究中,规模较小的研究有获得阳性结果的趋势,而大规模的全基因组多基因风险研究则有发现阴性结果的趋势。BD领域的神经影像学遗传学正在迅速发展。