TY - JOUR
T1 - 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
AU - Christensen, Jennaya
AU - Beveridge, Jaimie K.
AU - Wang, Melinda
AU - Orr, Serena L.
AU - Noel, Melanie
AU - Mychasiuk, Richelle
N1 - Funding Information:
Funding: This research was supported by funding awarded to M. Noel from the Vi Riddell Pediatric Pain Initiative (Grant #1036777), Alberta Children’s Hospital Foundation and Alberta Children’s Hospital Research Institute (Grant #1042861), and the Canadian Institutes of Health Research Strategy for Patient-Oriented Research ‘Chronic Pain Network’ (Grant #1041605); and to R. Mychasiuk from the Canadian Institutes of Health Research (PJT-153051).
Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/6
Y1 - 2021/6
N2 - 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.
AB - 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.
KW - ACEs
KW - Adolescents
KW - Biomarker
KW - Children
KW - Dopamine
KW - Epigenetics
KW - Parents
KW - PTSD
KW - Trauma
UR - http://www.scopus.com/inward/record.url?scp=85124311737&partnerID=8YFLogxK
U2 - 10.3390/epigenomes5020009
DO - 10.3390/epigenomes5020009
M3 - Article
C2 - 34968296
AN - SCOPUS:85124311737
SN - 2075-4655
VL - 5
JO - Epigenomes
JF - Epigenomes
IS - 2
M1 - 9
ER -