2015
DOI: 10.1073/pnas.1506352112
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Genetic variation in CD38 and breastfeeding experience interact to impact infants’ attention to social eye cues

Abstract: Attending to emotional information conveyed by the eyes is an important social skill in humans. The current study examined this skill in early development by measuring attention to eyes while viewing emotional faces in 7-mo-old infants. In particular, we investigated individual differences in infant attention to eyes in the context of genetic variation (CD38 rs3796863 polymorphism) and experiential variation (exclusive breastfeeding duration) related to the oxytocin system. Our results revealed that, whereas i… Show more

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Cited by 58 publications
(64 citation statements)
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References 93 publications
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“…Another region in BTA06 showing selection signal with the XP‐EHH methodology in two clusters, Colombian group (region #5) and Texas Longhorn (region #41), has not been associated with any QTL in cattle so far and includes genes such as C1QTNF7 , related to Trypanosoma cruzi cardiomyopathy (Deng et al., ), FBXL5 , which controls iron metabolism processes key for the regulation of reactive oxygen species that augment with the exposure of animals to high environmental temperatures (Paital et al., ), BST1 that has immune functions facilitating pre‐B‐cell growth, and CD38 that has pleiotropic functions in T‐cell activation (Würsch et al., ), social behaviour through its effect on the release of oxytocin (Krol, Monakhov, Lai, Ebstein, & Grossmann, ) and cancer. BST1 and CD38 are also implicated in salivary and pancreatic secretion and nicotinate and nicotinamide metabolism pathways (Table ).…”
Section: Resultsmentioning
confidence: 99%
“…Another region in BTA06 showing selection signal with the XP‐EHH methodology in two clusters, Colombian group (region #5) and Texas Longhorn (region #41), has not been associated with any QTL in cattle so far and includes genes such as C1QTNF7 , related to Trypanosoma cruzi cardiomyopathy (Deng et al., ), FBXL5 , which controls iron metabolism processes key for the regulation of reactive oxygen species that augment with the exposure of animals to high environmental temperatures (Paital et al., ), BST1 that has immune functions facilitating pre‐B‐cell growth, and CD38 that has pleiotropic functions in T‐cell activation (Würsch et al., ), social behaviour through its effect on the release of oxytocin (Krol, Monakhov, Lai, Ebstein, & Grossmann, ) and cancer. BST1 and CD38 are also implicated in salivary and pancreatic secretion and nicotinate and nicotinamide metabolism pathways (Table ).…”
Section: Resultsmentioning
confidence: 99%
“…Similar in this context is the role of breastfeeding. Although much research emphasized the positive effects of breastfeeding on the formation of mother-infant synchrony, the infant's social gaze (Feldman and Eidelman, 2003;Krol et al, 2015) and the development of cognitive competencies up to adulthood (Johnson et al, 1996;Mortensen et al, 2002), while bonding in rodents critically depends on lactation, human mothers can bond to their infants in the absence of breastfeeding via multiple alternative pathways and other forms of caregiving.…”
Section: Accepted Manuscriptmentioning
confidence: 99%
“…Why infant CD38 genotype did not have an impact on infants' cortisol response remains unclear. However, it should be mentioned that in prior work with older infants (7 months of age), infant CD38 genotype has been shown to impact differences in infants' attention to emotional eyes as a function of duration of exclusive breastfeeding (Krol et al 2015a). This indicates that in a different context (emotion perception and exclusive breastfeeding duration) and at an older age (7 instead of 4-6 months of age) infant CD38 genotype has an effect on socio-emotional processes.…”
Section: Discussionmentioning
confidence: 99%
“…Hardy-Weinberg equilibrium was tested in mothers and infants separately; no deviations were detected (all p-values >0.05). The majority of studies relating the polymorphism rs3796863 (CD38) with aspects of social behavior and plasma oxytocin find differences between homozygous risk allele carriers (CC) and A carriers (CA/AA) (Algoe and Way 2014;Feldman et al 2013;Feldman et al 2012;Krol et al 2015a;Sauer et al 2013;Sauer et al 2012). In keeping with prior studies, we conducted our analyses by grouping genotypes in the same manner (CC versus CA/AA).…”
Section: Methodsmentioning
confidence: 99%
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