一项初步研究调查性别在基因表达、慢性疼痛和不良童年经历之间的代际关系中的作用,在一个患有慢性疼痛的青少年临床样本中。

IF 2.5 Q3 GENETICS & HEREDITY
Jennaya Christensen, Jaimie K Beveridge, Melinda Wang, Serena L Orr, Melanie Noel, Richelle Mychasiuk
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引用次数: 6

摘要

慢性疼痛是一个非常普遍和昂贵的问题,经常出现在童年或青春期,并持续到成年。不良童年经历(ace)会增加几种不良健康状况的风险,包括慢性疼痛。最近的证据表明,父母的创伤(ace,创伤后应激障碍(PTSD)症状)会给他们的孩子带来不良健康结果的风险。父母创伤与儿童慢性疼痛之间的代际关系可能通过表观遗传机制介导。有慢性疼痛的青少年及其父母的临床样本完成了心理测量学上健全的问卷,评估ace、PTSD症状和慢性疼痛,并提供了唾液样本。这些被用来研究四种表观遗传生物标志物(COMT、DRD2、GR和SERT)、创伤和慢性疼痛之间的代际关系。结果表明,显著的生物标志物依赖于儿童的性别,其中父母ace与女性儿童DRD2表达的变化和男性儿童父母COMT表达的变化显著相关。此外,ACE的性质(虐待与家庭功能障碍)与特定的表观遗传变化有关。父母的ace可能通过不同的途径给男性和女性带来不良后果的风险,这突出了儿童性别在未来调查中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Pilot Study Investigating the Role of Gender in the Intergenerational Relationships between Gene Expression, Chronic Pain, and Adverse Childhood Experiences in a Clinical Sample of Youth with Chronic Pain.

Chronic pain is a highly prevalent and costly issue that often emerges during childhood or adolescence and persists into adulthood. Adverse childhood experiences (ACEs) increase risk for several adverse health conditions, including chronic pain. Recent evidence suggests that parental trauma (ACEs, post-traumatic stress disorder (PTSD) symptoms) confers risk of poor health outcomes in their children. Intergenerational relationships between parental trauma and child chronic pain may be mediated by epigenetic mechanisms. A clinical sample of youth with chronic pain and their parents completed psychometrically sound questionnaires assessing ACEs, PTSD symptoms, and chronic pain, and provided a saliva sample. These were used to investigate the intergenerational relationships between four epigenetic biomarkers (COMT, DRD2, GR, and SERT), trauma, and chronic pain. The results indicated that the significant biomarkers were dependent upon the gender of the child, wherein parental ACEs significantly correlated with changes in DRD2 expression in female children and altered COMT expression in the parents of male children. Additionally, the nature of the ACE (maltreatment vs. household dysfunction) was associated with the specific epigenetic changes. There may be different pathways through which parental ACEs confer risk for poor outcomes for males and females, highlighting the importance of child gender in future investigations.

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来源期刊
Epigenomes
Epigenomes GENETICS & HEREDITY-
CiteScore
3.80
自引率
0.00%
发文量
38
审稿时长
11 weeks
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