scholarly journals DRD2, DAT1, COMT, and OXTR Genes as Potential Moderators of the Relationship Between Maternal History of Maltreatment and Infant Emotion Regulation

2021 ◽  
Author(s):  
Vanessa Villani

Background: Gene-environment (GXE) interaction models have demonstrated that DRD2, DAT1, COMT, and OXTR SNPs moderate parental factors (i.e., maternal depression, parenting) to predict outcomes related to emotion regulation (e.g., affective problems, attentional control). No studies have investigated the connections between maternal maltreatment history and infant dopamine and oxytocin gene variants as they relate to infant emotion regulation. The current study addresses these gaps, evaluating the interaction of selected genes as they interact with maternal history of maltreatment to predict infant emotion regulation. Method: I investigated five infant genotypes (DRD2, DAT1, COMT, OXTR rs53576, and OXTR rs2254298) as they interacted with maternal history of self-reported maltreatment to predict observed infant emotion regulation behaviours. Self-reported maternal depressive symptoms were covaried. Infant emotion regulation was observed in the context of a potent stressor. I assessed three potential models of interaction, diathesis-stress, differential sensitivity, or vantage sensitivity. Results: Analyses demonstrated that, over and above maternal depressive symptoms, DRD2 and COMT significantly interacted with self-reported maternal maltreatment scores in a ‘vantage sensitivity’ model and DAT1 significantly interacted with maternal maltreatment history in a ‘diathesis-stress’ model. A cumulative vantage sensitivity (CVS) index significantly interacted with maternal maltreatment history to predict emotion regulation scores, consistent with a vantage sensitivity model. Conclusions: Findings indicated that infants with the “vantage” DRD2 (A1+) and COMT (Met) alleles, when exposed to mothers with lesser histories of maltreatment, fair better in terms of regulation than their non-susceptible counterparts. Infants with the “risk” DAT1 (presence of the 9-repeat) allele, when exposed to a parent with a greater history of maltreatment, tended to fare worse in terms of regulation behaviours. These differences in genetic interaction models suggest that an adaptive variation in genetic vulnerability and vantage-sensitivity, across an infant’s genome, can increase the possibility for optimal self-regulation outcomes, whether the environment is favourable or less favourable (i.e., lower versus higher history of maternal maltreatment, respectively).

2021 ◽  
Author(s):  
Vanessa Villani

Background: Gene-environment (GXE) interaction models have demonstrated that DRD2, DAT1, COMT, and OXTR SNPs moderate parental factors (i.e., maternal depression, parenting) to predict outcomes related to emotion regulation (e.g., affective problems, attentional control). No studies have investigated the connections between maternal maltreatment history and infant dopamine and oxytocin gene variants as they relate to infant emotion regulation. The current study addresses these gaps, evaluating the interaction of selected genes as they interact with maternal history of maltreatment to predict infant emotion regulation. Method: I investigated five infant genotypes (DRD2, DAT1, COMT, OXTR rs53576, and OXTR rs2254298) as they interacted with maternal history of self-reported maltreatment to predict observed infant emotion regulation behaviours. Self-reported maternal depressive symptoms were covaried. Infant emotion regulation was observed in the context of a potent stressor. I assessed three potential models of interaction, diathesis-stress, differential sensitivity, or vantage sensitivity. Results: Analyses demonstrated that, over and above maternal depressive symptoms, DRD2 and COMT significantly interacted with self-reported maternal maltreatment scores in a ‘vantage sensitivity’ model and DAT1 significantly interacted with maternal maltreatment history in a ‘diathesis-stress’ model. A cumulative vantage sensitivity (CVS) index significantly interacted with maternal maltreatment history to predict emotion regulation scores, consistent with a vantage sensitivity model. Conclusions: Findings indicated that infants with the “vantage” DRD2 (A1+) and COMT (Met) alleles, when exposed to mothers with lesser histories of maltreatment, fair better in terms of regulation than their non-susceptible counterparts. Infants with the “risk” DAT1 (presence of the 9-repeat) allele, when exposed to a parent with a greater history of maltreatment, tended to fare worse in terms of regulation behaviours. These differences in genetic interaction models suggest that an adaptive variation in genetic vulnerability and vantage-sensitivity, across an infant’s genome, can increase the possibility for optimal self-regulation outcomes, whether the environment is favourable or less favourable (i.e., lower versus higher history of maternal maltreatment, respectively).


2021 ◽  
Author(s):  
Jaclyn Ludmer

Background: This dissertation examines maternal genotypes and mother-infant attachment as moderators of the association between the early rearing environment and cortisol secretion. Study 1 examines whether DRD2, SLC6A3, and OXTR genes moderate the association between maternal history of care and maternal cortisol secretion. Study 2 examines mother-infant attachment as a moderator of the associations between maternal depressive symptoms and both infant and maternal cortisol secretion. Method: Mothers self-reported their history of care and depressive symptoms at infant age 16 months. At 17 months, mother-infant attachment was assessed in the Strange Situation Procedure (SSP). Salivary cortisol was assessed at baseline and at 20- and 40-minutes post-SSP. Buccal cells were collected for genotyping. Results: Study 1 revealed that maternal history of low care predicts elevated cortisol secretion, but only for mothers with 10-repeat alleles of SLC6A3 or G alleles of OXTR. Study 2 revealed that maternal depressive symptoms predict elevated cortisol secretion, but only for infants and mothers in non-secure attachment relationships. Conclusions: This dissertation enhances our understanding of the complex relations between the early rearing environment and maternal and infant cortisol secretion.


2021 ◽  
Author(s):  
Jaclyn Ludmer

Background: This dissertation examines maternal genotypes and mother-infant attachment as moderators of the association between the early rearing environment and cortisol secretion. Study 1 examines whether DRD2, SLC6A3, and OXTR genes moderate the association between maternal history of care and maternal cortisol secretion. Study 2 examines mother-infant attachment as a moderator of the associations between maternal depressive symptoms and both infant and maternal cortisol secretion. Method: Mothers self-reported their history of care and depressive symptoms at infant age 16 months. At 17 months, mother-infant attachment was assessed in the Strange Situation Procedure (SSP). Salivary cortisol was assessed at baseline and at 20- and 40-minutes post-SSP. Buccal cells were collected for genotyping. Results: Study 1 revealed that maternal history of low care predicts elevated cortisol secretion, but only for mothers with 10-repeat alleles of SLC6A3 or G alleles of OXTR. Study 2 revealed that maternal depressive symptoms predict elevated cortisol secretion, but only for infants and mothers in non-secure attachment relationships. Conclusions: This dissertation enhances our understanding of the complex relations between the early rearing environment and maternal and infant cortisol secretion.


2020 ◽  
Vol 51 (5) ◽  
pp. 792-800
Author(s):  
Arielle H. Sheftall ◽  
Emory E. Bergdoll ◽  
Monaé James ◽  
Connor Bauer ◽  
Elisabeth Spector ◽  
...  

2015 ◽  
pp. n/a-n/a ◽  
Author(s):  
Jennifer E. Khoury ◽  
Andrea Gonzalez ◽  
Robert Levitan ◽  
Mario Masellis ◽  
Vincenzo Basile ◽  
...  

2019 ◽  
Vol 29 (8) ◽  
pp. 1125-1134 ◽  
Author(s):  
Qiong Wu ◽  
Xin Feng ◽  
Micah Gerhardt ◽  
Li Wang

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