The relation between Oxytocin Receptor Gene polymorphisms, adult attachment and Instagram sociability: an exploratory analysis

So far literature considered the association between environmental factors (i.e. involved in adult relationships) and genetic vulnerability on Oxytocin Receptor Gene (OXTR) in the comprehension of social behavior. Although an extensive knowledge on in-person social interactions has been obtained, little is known about online social behavior. A gene-environment perspective is adopted to examine how OXTR and adult attachment moderate Instagram behavior. The Experience in Close Relationships-Revised (ECR-R) questionnaire was used to collect participants' (N = 57, 16 males) attachment with their partners. The genetic factors within the regions OXTR rs53576 (A/A homozygotes vs. G-carriers) and rs2254298 (G/G homozygotes vs. A-carriers) were assessed. Number of posts, followed people ("followings") and followers were obtained from Instagram, and the Social Desirability Index was calculated as the ratio of followers to followings. Interaction effects between OXTR groups and ECR-R scores on the number of posts and SDI were hypothesised. Results showed an effect of rs53576 on the number of Instagram followings. Specifically, A/A homozygotes had more followings than G-carriers independently of the quality of the relationship with their partner. These preliminary results are discussed in light of the debate of behavioral genetics and offer insights into future investigations on social media behavior.

Social Anxiety and Common OXTR Gene Variant are Associated with Cortisol Response Following Peer Social Challenge

Peer rejection and acceptance experiences are commonplace with potential to promote emotional and adrenocortical stress reactivity. Risk for heightened stress reactivity during these social challenges may be influenced by individual differences in social interaction anxiety (SIA) and the common gene variant, OXTR rs53576, but this relationship remains to be elucidated. We tested the relationship between SIA, OXTR rs53576, and cortisol stress response over time in 53 young adults (Mage=20.13yrs) using an experimental design. Participants were randomized to receive either scripted rejection or acceptance from a group of peer confederates. Saliva samples were collected pre- and post-evaluation and assayed for cortisol. In the peer rejection condition, participants showed significantly lower cortisol responses over time when social interaction anxiety levels were not elevated (versus elevated), and when possessing the GG genotype (versus AA/AG). In the peer acceptance condition, when SIA was not elevated, the GG genotype was associated with significantly lower cortisol responses than the AA/AG genotype. Individual differences in SIA and OXTR 53576 are related to cortisol responses to peer social stressors, with non-elevated levels of SIA and the GG genotype generally contributing to reduced cortisol responsiveness.

OXTR rs53576 variation with breast and nipple pain in breastfeeding women

Purpose: To evaluate associations among breast and nipple pain sensitivity and candidate pain sensitivity single-nucleotide polymorphisms [SNPs], (COMT rs6269, rs4633, rs4818, rs4680 and OXTR rs2254298, rs53576) in breastfeeding women. Design: A secondary analysis of sixty women participating in a pilot randomized controlled trial of a pain self-management intervention. Methods: All participants underwent standardized mechanical somatosensory testing for an assessment of pain sensitivity and provided baseline buccal swabs for genetic analysis. At 1, 2, and 6 weeks postpartum, women self-reported breast and nipple pain severity using a visual analogue scale. Results:- Women with the minor allele OXTR rs53576 reported 8.18-fold higher breast and nipple pain severity over time. For every 1-unit increase in mechanical detection threshold and windup ratio, women reported 16.51-fold and 4.82-fold higher breast and nipple pain severity respectively. Six women with the OXTR rs2254298 minor allele reported allodynia. Discussion: The presence of OXTR alleles in women with enhanced pain sensitivity suggests a phenotype of genetic risk for ongoing breast and nipple with potential for pain-associated breastfeeding cessation. Somatosensory testing identified women who reported higher breast and nipple pain during the first weeks of breastfeeding. Clinical Implications: Pain sensitivity testing can help to identify women at risk of intolerable and/or ongoing breastfeeding pain who may benefit from additional support to mitigate early breastfeeding cessation. Targeted interventions are needed to address breastfeeding pain, including management of infant latch, positioning, and infection as well as support for self-management of breastfeeding pain.

Oxytocin Pathway Genes (CD38, OXTR) and Psychosocial Characteristics Defined According to Strengths and Difficulties Questionnaire in Urban Siberian Adolescents: A School-based Study

Oxytocin (OT) is regarded as an extremely important prosocial neuropeptide that dramatically affects the establishment of social connections from infancy to adulthood. OT effects on the psychoemotional state are pretty individual and may be dependent on age, gender, ethnocultural factors, social environment, the presence of stress factors, and features of personality. The Strengths and Difficulties Questionnaire (SDQ) is a brief psychopathological screening tool and is recommended for the detection and classification of psychosocial problems in adolescents. The current field school-based study, conducted among urban Siberian adolescents (n = 298 aged 12–18) explored the relation of SDQ scales in relation to genotypes of CD38 gene that controls oxytocin release, rs3796863, and oxytocin receptor gene (OXTR), rs53576. The results of our study show that during the adolescence period, OT pathway high activity can cause some negative effects, such as emotional instability in young (aged 12–14) adolescent girls in the case of carriage of the rs3796863 A allele and emotional disturbances in older (aged 15–18) adolescent boys who are carriers of a GG variant of rs53576. Our results support the hypothesis of OT-mediated excessive social sensitivity which can lead to some age-sex depending psychosocial problems during adolescence.

Association Analysis of 14 Candidate Gene Polymorphism with Depression and Stress among Gestational Diabetes Mellitus

The association of candidate genes and psychological symptoms of depression, anxiety, and stress among women with gestational diabetes mellitus (GDM) in Malaysia was determined in this study, followed by the determination of their odds of getting psychological symptoms, adjusted for socio-demographical background, maternal, and clinical characteristics. Single nucleotide polymorphisms (SNPs) recorded a significant association between SNP of EPHX2 (rs17466684) and depression symptoms (AOR = 7.854, 95% CI = 1.330–46.360) and stress symptoms (AOR = 7.664, 95% CI = 1.579–37.197). Associations were also observed between stress symptoms and SNP of OXTR (rs53576) and (AOR = 2.981, 95% CI = 1.058–8.402) and SNP of NRG1 (rs2919375) (AOR = 9.894, 95% CI = 1.159–84.427). The SNP of EPHX2 (rs17466684) gene polymorphism is associated with depression symptoms among Malaysian women with GDM. SNP of EPHX2 (rs17466684), OXTR (rs53576) and NRG1 (rs2919375) are also associated with stress symptoms.