Bainomugisa Charlotte K, Sutherland Heidi G, Parker Richard, Mcrae Allan F, Haupt Larisa M, Griffiths Lyn R, Heath Andrew, Nelson Elliot C, Wright Margaret J, Hickie Ian B, Martin Nicholas G, Nyholt Dale R, Mehta Divya
Centre for Genomics and Personalised Health, School of Biomedical Science, Faculty of Health, Queensland University of Technology, Kelvin Grove, QLD, Australia.
Centre for Genomics and Personalised Health, Genomics Research Centre, School of Biomedical Sciences, Institute of Health and Biomedical Innovation, Kelvin Grove, QLD, Australia.
Front Neurosci. 2021 Jun 22;15:678350. doi: 10.3389/fnins.2021.678350. eCollection 2021.
Epigenetic mechanisms have been associated with genes involved in Posttraumatic stress disorder (PTSD). PTSD often co-occurs with other health conditions such as depression, cardiovascular disorder and respiratory illnesses. PTSD and migraine have previously been reported to be symptomatically positively correlated with each other, but little is known about the genes involved. The aim of this study was to understand the comorbidity between PTSD and migraine using a monozygotic twin disease discordant study design in six pairs of monozygotic twins discordant for PTSD and 15 pairs of monozygotic twins discordant for migraine. DNA from peripheral blood was run on Illumina EPIC arrays and analyzed. Multiple testing correction was performed using the Bonferroni method and 10% false discovery rate (FDR). We validated 11 candidate genes previously associated with PTSD including , , and 1. In the epigenome-wide scan, seven novel CpGs were significantly associated with PTSD within/near , , , , , and , with all CpGs except the CpG hypermethylated in PTSD. These results were significantly enriched for genes whose DNA methylation was previously associated with migraine (-value = 0.036). At 10% FDR, 132 CpGs in 99 genes associated with PTSD were also associated with migraine in the migraine twin samples. Genes associated with PTSD were overrepresented in vascular smooth muscle, axon guidance and oxytocin signaling pathways, while genes associated with both PTSD and migraine were enriched for AMPK signaling and longevity regulating pathways. In conclusion, these results suggest that common genes and pathways are likely involved in PTSD and migraine, explaining at least in part the co-morbidity between the two disorders.
表观遗传机制与创伤后应激障碍(PTSD)相关基因有关。PTSD常与其他健康状况同时出现,如抑郁症、心血管疾病和呼吸系统疾病。此前有报道称PTSD和偏头痛在症状上呈正相关,但对其中涉及的基因了解甚少。本研究的目的是利用单卵双生子疾病不一致研究设计,对6对患PTSD不一致的单卵双生子和15对患偏头痛不一致的单卵双生子进行研究,以了解PTSD和偏头痛之间的共病情况。从外周血提取的DNA在Illumina EPIC芯片上进行检测并分析。使用Bonferroni方法和10%的错误发现率(FDR)进行多重检验校正。我们验证了11个先前与PTSD相关的候选基因,包括[具体基因1]、[具体基因2]和[具体基因3]。在全表观基因组扫描中,7个新的CpG位点在[基因1]、[基因2] [基因3]、[基因4]、[基因5]和[基因6]内部或附近与PTSD显著相关,除了[具体CpG位点]外,所有CpG位点在PTSD中均发生高甲基化。这些结果在DNA甲基化先前与偏头痛相关的基因中显著富集(P值 = 0.036)。在10%的FDR水平下,99个与PTSD相关基因中的m132个CpG位点在偏头痛双生子样本中也与偏头痛相关。与PTSD相关的基因在血管平滑肌、轴突导向和催产素信号通路中过度表达,而与PTSD和偏头痛都相关的基因在AMPK信号通路和寿命调节通路中富集。总之,这些结果表明,PTSD和偏头痛可能涉及共同的基因和通路,这至少部分解释了这两种疾病之间的共病现象。