Hyperarousal Symptom Severity in Women with Posttraumatic Stress Disorder Might Be Associated with LINE-1 Hypomethylation in Childhood Sexual Abuse Victims.

Complex psychiatry Pub Date : 2023-02-15 eCollection Date: 2023-01-01 DOI:10.1159/000529698
Carolina Muniz Carvalho, Bruno Messina Coimbra, Amanda Bugiga, Diogo Ferri Marques, Vanessa Kiyomi Ota, Andrea Feijó Mello, Marcelo Feijó Mello, Sintia Iole Belangero
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Abstract

Introduction: Sexual assault and a history of childhood sexual abuse (CSA) are related to posttraumatic stress disorder (PTSD) development. Long interspersed nuclear elements (LINE-1) are transposable elements, and their methylation is used to infer DNA global methylation. DNA methylation can be affected by trauma exposition which in turn would be associated with PTSD. Thus, we investigated if the LINE-1 methylation pattern is related to PTSD symptoms in females with a history of CSA.

Methods: This is a case-control study that examined, at baseline (W1), 64 women victims of sexual assault diagnosed with PTSD and 31 patients with PTSD who completed the 1-year follow-up (W2). Participants were categorized into two groups according to the presence of CSA (PTSDCSA+: NW1 = 19, NW2 = 10; PTSDCSA-: NW1 = 45, NW2 = 21). PTSD symptoms (re-experiencing, avoidance, hyperarousal, alterations in cognition/mood) were assessed using the Clinician-Administered PTSD Scale, and the history of CSA was assessed by the Childhood Trauma Questionnaire. LINE-1 methylation was measured in three sites (CpG1, CpG2, CpG3) located in the 5'UTR region using bisulfite conversion followed by pyrosequencing. Linear regression models were performed to test the relation between LINE-1 CpG sites methylation and PTSD symptoms.

Results: We found a negative association between CpG2 methylation and hyperarousal symptoms among those in the PTSDCSA+ group in W1 (adjusted p = 0.003) compared to the PTSDCSA- group (p > 0.05). Still, no association was observed between other PTSD symptoms and other CpG sites. Further, in the longitudinal analysis, LINE-1 hypomethylation was no longer observed in PTSD participants exposed to CSA.

Conclusion: Our findings suggest that LINE-1 methylation may help understand the relationship between trauma and PTSD. However, more studies are needed to investigate LINE-1 as an epigenetic marker of psychiatric disorders.

创伤后应激障碍女性的过度焦虑症状严重程度可能与童年性虐待受害者体内 LINE-1 基因的低甲基化有关
导言:性侵犯和童年性虐待(CSA)史与创伤后应激障碍(PTSD)的发展有关。长穿插核元素(LINE-1)是一种转座元件,其甲基化可用于推断 DNA 的全局甲基化。DNA甲基化会受到创伤暴露的影响,而创伤暴露又会与创伤后应激障碍有关。因此,我们研究了LINE-1甲基化模式是否与有CSA史的女性的创伤后应激障碍症状有关:这是一项病例对照研究,对基线(W1)时被诊断为创伤后应激障碍的 64 名女性性侵犯受害者和完成 1 年随访(W2)的 31 名创伤后应激障碍患者进行了研究。根据是否存在 CSA 将参与者分为两组(PTSDCSA+:NW1 = 19,NW2 = 10;PTSDCSA-:NW1 = 45,NW2 = 21)。创伤后应激障碍症状(再体验、回避、过度焦虑、认知/情绪改变)通过临床医师管理的创伤后应激障碍量表进行评估,CSA史通过童年创伤问卷进行评估。利用亚硫酸氢盐转化法和热释光测序法测量了位于5'UTR区域的三个位点(CpG1、CpG2和CpG3)的LINE-1甲基化情况。通过线性回归模型检验了LINE-1 CpG位点甲基化与创伤后应激障碍症状之间的关系:结果:我们发现,与 PTSDCSA- 组(p > 0.05)相比,W1 组中 PTSDCSA+ 组的 CpG2 甲基化与过度焦虑症状呈负相关(调整后 p = 0.003)。然而,在其他创伤后应激障碍症状和其他 CpG 位点之间没有观察到任何关联。此外,在纵向分析中,暴露于 CSA 的创伤后应激障碍参与者中不再观察到 LINE-1 低甲基化:我们的研究结果表明,LINE-1甲基化可能有助于理解创伤与创伤后应激障碍之间的关系。结论:我们的研究结果表明,LINE-1甲基化可能有助于理解创伤与创伤后应激障碍之间的关系,但还需要更多的研究来探讨LINE-1作为精神疾病表观遗传标记的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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