[HTML][HTML] Environmental risk, Oxytocin Receptor Gene (OXTR) methylation and youth callous-unemotional traits: a 13-year longitudinal study

CAM Cecil, LJ Lysenko, SR Jaffee, JB Pingault… - Molecular …, 2014 - nature.com
CAM Cecil, LJ Lysenko, SR Jaffee, JB Pingault, RG Smith, CL Relton, G Woodward…
Molecular psychiatry, 2014nature.com
Youth with high callous-unemotional traits (CU) are at risk for early-onset and persistent
conduct problems. Research suggests that there may be different developmental pathways
to CU (genetic/constitutional vs environmental), and that the absence or presence of co-
occurring internalizing problems is a key marker. However, it is unclear whether such a
distinction is valid. Intermediate phenotypes such as DNA methylation, an epigenetic
modification regulating gene expression, may help to clarify etiological pathways. This is the …
Abstract
Youth with high callous-unemotional traits (CU) are at risk for early-onset and persistent conduct problems. Research suggests that there may be different developmental pathways to CU (genetic/constitutional vs environmental), and that the absence or presence of co-occurring internalizing problems is a key marker. However, it is unclear whether such a distinction is valid. Intermediate phenotypes such as DNA methylation, an epigenetic modification regulating gene expression, may help to clarify etiological pathways. This is the first study to examine prospective inter-relationships between environmental risk (prenatal/postnatal) and DNA methylation (birth, age 7 and 9) in the prediction of CU (age 13), for youth low vs high in internalizing problems. We focused on DNA methylation in the vicinity of the oxytocin receptor (OXTR) gene as it has been previously implicated in CU. Participants were 84 youth with early-onset and persistent conduct problems drawn from the Avon Longitudinal Study of Parents and Children. For youth with low internalizing problems (46%), we found that (i) OXTR methylation at birth associated with higher CU (age 13) as well as decreased experience of victimization during childhood (evocative epigenetic-environment correlation; birth–age 7),(ii) higher prenatal parental risks (maternal psychopathology, criminal behaviors, substance use) associated with higher OXTR methylation at birth and (iii) OXTR methylation levels were more stable across time (birth–age 9). In contrast, for youth with high internalizing problems, CU were associated with prenatal risks of an interpersonal nature (that is, intimate partner violence, family conflict) but not OXTR methylation. Findings support the existence of distinct developmental pathways to CU.
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