School for Mental Health and Neuroscience, Faculty of Health, Medicine and Life Sciences, Maastricht University, 6211 LK Maastricht, The Netherlands.
NORMENT, Division of Mental Health and Addiction, Oslo University Hospital & Institute of Clinical Medicine, University of Oslo, 0315 Oslo, Norway.
Genes (Basel). 2022 Nov 2;13(11):2003. doi: 10.3390/genes13112003.
22q11.2 deletion syndrome (22q11DS) is a clinically heterogeneous genetic syndrome, associated with a wide array of neuropsychiatric symptoms. The clinical presentation is likely to be influenced by environmental factors, yet little is known about this. Here, we review the available research literature on the role of the environment in 22q11DS. We find that within-patient design studies have mainly investigated the role of parental factors, stress, and substance use, reporting significant effects of these factors on the clinical profile. Case-control studies have been less successful, with almost no reports of significant moderating effects of the environment. We go on to hypothesize which specific environmental measures are most likely to interact with the 22q11 deletion, based on the genes in this region and their involvement in molecular pathways. We end by discussing potential reasons for the limited findings so far, including modest sample sizes and limited availability of environmental measures, and make recommendations how to move forward.
22q11.2 缺失综合征(22q11DS)是一种临床表现多样的遗传性综合征,与广泛的神经精神症状相关。环境因素可能会影响其临床表现,但目前对此知之甚少。在这里,我们回顾了关于环境在 22q11DS 中作用的现有研究文献。我们发现,基于患者内的设计研究主要调查了父母因素、压力和物质使用的作用,报告了这些因素对临床特征的显著影响。病例对照研究的结果则不太成功,几乎没有报道环境有显著的调节作用。在此基础上,我们根据该区域的基因及其在分子途径中的作用,进一步假设哪些特定的环境因素最有可能与 22q11 缺失相互作用。最后,我们讨论了迄今为止发现有限的潜在原因,包括样本量较小和环境测量的可用性有限,并提出了如何推进研究的建议。