Attachment Epigenetics Neuroscience Psychology

Towards the Epigenetics of Human Attachment

Attachment theory postulates that the establishment of attachment bonds represents an innate, biologically programmed behaviour. Its biological function is to enhance the chances of survival in times of danger and need. Accordingly, (almost) all children become attached to an attachment figure – mostly a caregiver – to survive. However, beyond such basic biological function associated with survival, attachment theory emphasises the existence of considerable interindividual differences in attachment quality. These interindividual differences in attachment quality are usually captured through secure versus insecure – anxious and avoidant – attachment orientations, and are associated with universal strategies to either draw near, or away, from significant others during situations of personal distress. For a more detailed overview on attachment theory and its terminology (also from a social neuroscience perspective), please see here.

Since Bowlby’s pioneering writings on the theory of attachment, attachment researchers have been intrigued by the question how secure versus insecure attachment orientations emerge during human development. The most plausible explanation considers both genetic and social factors, in that, as Jay Belsky puts it elegantly in one of his blog posts: “it appears that some children are simply born secure, whereas others are made secure or insecure by, as theory would have it, the quality of rearing they experience“.

The above view that secure versus insecure attachment orientations emerge during development depending on both genetic and social factors was neatly demonstrated by the seminal work of Weaver and colleagues in rodents (original publications: 1999 and 2004). A comprehensive  and interactive online summary is available from the University of Utah Genetic Science Learning Center via the website  “Lick Your Rats“.

Weaver and colleagues selected rat mothers by naturally occurring interindividual differences in maternal behaviour, quantified by low versus high licking and grooming (LG) and arched-back nursing (ABN). Within this context, a high LG-ABN rat mother would most closely resemble a sensitive / available human mother and thus a rearing environment favouring the emergence of a secure attachment in the offspring. In turn, a low LG-ABN rat mother would most closely resemble an insensitive / unavailable human mother and thus a rearing environment favouring the emergence of an insecure attachment in the offspring.

The researchers then examined adult pups of low and high LG-ABN rat mothers that were either brought up by their own / biological mother, or reared by a foster mother. In so doing, the researchers found that some pups were “born secure” (i.e., adult pups from a high LG-ABN mother reared by a low LG-ABN foster mother resembled adult pups born and reared by a high LG-ABN mother), whilst others “were made secure by the quality of rearing” (i.e., adult pups from a low LG-ABN mother reared by a high LG-ABN foster mother resembled adult pups born and reared by a high LG-ABN mother). 

In addition to showing the above patterns based on observing the adult rat pups’ behaviour, Weaver and colleagues also provided an underlying biological mechanism reflecting a gene by environment interaction. They found that the environment’s influence on pup development was maintained by non-genomic transmission of interindividual differences in terms of epigenetic DNA modification. Specifically, they observed that expression of the glucocorticoid receptor – an important component of the HPA axis regulating stress – was altered in rat pups through DNA methylation, thereby determining how strongly the rat pups responded to stress during adulthood. 

Since Weaver and colleagues reported the above findings in rodents, some evidence for a similar mechanism involving epigenetic modification of the glucocorticoid receptor has been found in humans post-mortem (associated with childhood abuse). It therefore appears that both genetic and social factors play a role in human development, too. A nice overall summary mentioning the experiments in low versus high LG-ABN rats, and more generally discussing the associated nature versus nurture debate in relation to human development, can be found in this YouTube video (University of Oslo).

According to the above-described theoretical considerations and animal data, we set out to investigate whether we could find evidence for a gene by environment interaction in association with attachment in humans. To this end, we turned to attachment theory and its assumption that interindividual differences in attachment are associated with universal strategies to either draw near, or away, from significant others during situations of personal distress.

To capture the propensity to approach (or avoid) others, we used a biological marker associated with the oxytocin system, namely the oxytocin receptor gene (OXTR). As for the study in rodents, we then also examined the glucocorticoid receptor gene (NR3C1) associated with the HPA stress axis, and particularly the negative feedback loop to end the stress response. In both cases we looked at the degree of gene promoter methylation as a function of attachment security versus insecurity (i.e., attachment avoidance and anxiety), the latter obtained through an attachment self-report questionnaire. To analyse OXTR and NR3C1 promoter methylation, our participants – 109 young healthy adults (56 female) – provided saliva samples. 


What we observed was a specific effect for attachment avoidance: the higher our participants scored on attachment avoidance (i.e., high levels of attachment avoidance with concomitantly low levels of attachment anxiety), the more OXTR and NR3C1 promoter methylation was present. Furthermore, we did not find any differentiation between attachment security and anxiety – they both were linked to similar levels of OXTR and NR3C1 promoter methylation. The same was true for a combination of high attachment anxiety and avoidance.

Although these findings are preliminary and need replication and further extension, they tentatively suggest that attachment in humans could also be related to epigenetic DNA modification, particularly in two systems associated with the social regulation of stress. What is interesting is that attachment avoidance appears to be most strongly linked to OXTR and NR3C1 promoter methylation, with attachment avoidance most consistently showing links to diminished social responding and support-seeking in humans (see our NAMA model).

Caution is advised, however, when interpreting our findings, because they emerged from a correlational study and only reflect epigenetic DNA modification at one time point. We can therefore not establish any causal relationship between OXTR and NR3C1 promoter methylation and attachment (avoidance) in humans as of yet. These and some additional limitations are explicitly mentioned in the corresponding publication (see below).

Despite the currently present limitations, we think that the assessment of gene (promoter) methylation offers a promising new avenue to study gene by environment interactions in the context of human attachment, and hope that this approach may inform the development of future prevention and intervention strategies. This notion is supported by a recent review paper (Attachment and Epigenetics: A Scoping Review of Recent Research and Current Knowledge) by Rasmussen & Storebro (2020) that presents a broad perspective on the current state of knowledge in the relatively new and complex field of “attachment and epigenetic processes” in humans. The authors identified 11 studies on this topic performed since 2009 and summarised the so far available evidence in the format of a narrative / scoping review. While some communalities appear to emerge – such as a focus on the HPA stress axis and glucocorticoids or the oxytocin system – many questions still remain unresolved and need further investigation.

The above data were published in the following paper: 

Tsachi Ein-Dor, Willem J. M. I. Verbeke, Michal Mokry & Pascal Vrtička (2018). Epigenetic modification of the oxytocin and glucocorticoid receptor genes is linked to attachment avoidance in young adults. Attachment & Human Development.

Our paper is published open access and therefore freely available.

Dr Pascal Vrticka is a social neuroscientist with strong ties to developmental & social psychology. His research focuses on the psychological, behavioural, biological, and brain basis of human social interaction, attachment and caregiving. Besides measuring neurobiological responses to different kinds of social versus non-social information in single participants using (functional) magnetic resonance imaging ([f]MRI) and electroencephalography (EEG), Dr Vrticka most recently started to assess bio-behavioural synchrony in interacting pairs using functional near-infrared spectroscopy (fNIRS) hyperscanning. The main question thereby is how romantic partners and parents with their children get “in sync” when they solve problems together or talk to each other. Dr Vrticka furthermore relates the obtained individual and dyadic behavioural, biological, and brain measures to interindividual differences in relationship quality – particularly attachment and caregiving. In doing so, he refers to attachment theory that provides a suitable theoretical framework on how we initiate and maintain interpersonal relationships across the life span. With his research, Dr Vrticka is promoting a new area of investigation: the social neuroscience of human attachment.

1 comment on “Towards the Epigenetics of Human Attachment

  1. Pingback: Attachment and Epigenetics (Research) – PerSynthesis

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