Human Milk as a Pathway for Intergenerational Transmission: The Impact of Maternal Anxiety on Milk Immune Components and Infant Uncinate Fasciculus Microstructure

dc.contributor.authorCarreno, Claudia Adelitaen
dc.contributor.committeechairHowell, Brittany R.en
dc.contributor.committeememberBell, Martha Annen
dc.contributor.committeememberWallace, TeKisha Monet Riceen
dc.contributor.committeememberKatz, Benjamin D.en
dc.contributor.departmentAdult Learning and Human Resource Developmenten
dc.date.accessioned2026-06-06T08:00:29Zen
dc.date.available2026-06-06T08:00:29Zen
dc.date.issued2026-06-05en
dc.description.abstractInfancy is a unique time characterized by a profound link between mothers and infants. Infants rely on their mothers for all aspects of their survival, making mothers arguably the most salient influence in their lives. This close relationship provides infants with a range of beneficial resources for growth and development; however, when mothers lack access to resources to cope with stressors themselves, this can lead to adverse outcomes for infants. Traits such as anxiety, could either act as a resource for mothers (e.g., low trait anxiety) or a stressor (e.g., high trait anxiety). High trait anxiety may result in chronic activation of the stress response system due to evaluation of neutral stimuli as a threat. One result of chronic activation of stress is the dysregulation of the immune system, likely contributing to the long-term health outcomes we observe. Notably, human milk contains immune mediators such as Interleukin-6 and C-reactive protein, potentially exposing infants to maternal immune system function and, indirectly, to maternal stress. Though there is strong evidence that human milk supports healthy infant brain development, there is a paucity of information on the effects of increased exposure to immune system biomediators within milk, including which maternal factors may impact them. As immune biomediators influence developing white matter (WM) structure, specifically in areas that mediate our stress response, they may contribute to the development of adverse mental and physical health outcomes. Therefore, investigating tracts that connect regions involved in the stress response, such as the uncinate fasciculus (UF), may help characterize one pathway for the intergenerational transmission of stress. Utilizing maternal self-reports, milk samples, and infant diffusion tensor imaging during the first year postpartum from the UNC/UMN Baby Connectome Project, this dissertation sought to address two questions: 1) Does maternal trait anxiety impact concentrations of milk immune components, and 2) Do milk immune components impact infant UF fractional anisotropy (FA; an estimate of directional dependence of water reflecting myelin integrity) during the first-year post birth? Results from this study found no significant relationships between maternal trait anxiety and IL-6 presence (OR = 0.95, p = 0.15) but did find a significant positive relationship with CRP (B = 0.06, p = .048). The second, exploratory analysis found that presence of IL-6 was related to increased right UF FA (F(1,24) = 4.30, p = .050, η^2 = 0.16), but not left UF FA (F(1, 24) = 2.36, p = 0.138, η^2 = 0.10). These results provide evidence that maternal factors influence milk immune components and milk immune components influence infant neurodevelopment; however, more research is needed to definitively characterize these relationships.en
dc.description.abstractgeneralInfancy is a unique time characterized by a profound link between mothers and infants. Infants rely on their mothers for everything, making mothers arguably one of the most important influences in their lives. This close relationship provides infants with a range of resources for growth and development; however, when mothers do not have access to resources to cope with stressors, this can lead to adverse outcomes for infants later. Traits such as anxiety, could either act as a resource for mothers (e.g., low trait anxiety) or a stressor (e.g., high trait anxiety). High trait anxiety may result in chronic activation of the stress response system due to evaluation of neutral stimuli as a threat. One result of chronic activation of stress is immune system dysfunction, likely fueling the long-term health outcomes we observe. Notably, human milk contains immune system products such as Interleukin-6 and C-reactive protein, potentially exposing infants to maternal immune system functioning and, indirectly, to maternal stress. Though we know that milk supports healthy early neurodevelopment, little is known about how milk's immune system components affect infants and which maternal factors may influence them. The brain consists primarily of two types of tissue, known as white matter and grey matter. Grey matter refers to areas with a high amount of brain cells known as neurons, whereas white matter reflects the tissue with a high number of axons that connect different grey matter regions. As immune system products may affect developing white matter (WM) structure, specifically in areas that help our stress response, they may contribute to the development of negative health outcomes. Therefore, investigating white matter areas that connect grey matter regions involved in the stress response, such as the uncinate fasciculus (UF), may help us to understand the connection between maternal stress, immune system products, and the developing infant brain. Using maternal surveys, milk samples, and white matter measures during the first year postpartum from the UNC/UMN Baby Connectome Project, this dissertation aimed to address two questions: 1) Does maternal trait anxiety impact concentrations of milk immune products, and 2) Do milk immune products impact infant UF WM development during the first-year post birth? Results from this study found no significant relationships between maternal trait anxiety and IL-6 presence (OR = 0.95, p = 0.15) but did find a significant positive relationship with CRP (B = 0.06, p = .048). The second, exploratory analysis found that the presence of IL-6 was related to increased right UF WM development (F(1,24) = 4.30, p = .050, η^2 = 0.16), but not left UF WM development (F(1, 24) = 2.36, p = 0.138, η^2 = 0.10). There was no relationship between CRP and either right or left UF FA. These results provide evidence that maternal factors influence milk immune components, and milk immune components influence infant neurodevelopment; however, more research is needed to definitively characterize these relationships.en
dc.description.degreeDoctor of Philosophyen
dc.format.mediumETDen
dc.identifier.othervt_gsexam:47393en
dc.identifier.urihttps://hdl.handle.net/10919/143272en
dc.language.isoenen
dc.publisherVirginia Techen
dc.rightsCreative Commons Attribution 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en
dc.subjecthuman milken
dc.subjectanxietyen
dc.subjectuncinate fasciculusen
dc.subjectdiffusion MRIen
dc.subjectfractional anisotropyen
dc.titleHuman Milk as a Pathway for Intergenerational Transmission: The Impact of Maternal Anxiety on Milk Immune Components and Infant Uncinate Fasciculus Microstructureen
dc.typeDissertationen
thesis.degree.disciplineHuman Developmenten
thesis.degree.grantorVirginia Polytechnic Institute and State Universityen
thesis.degree.leveldoctoralen
thesis.degree.nameDoctor of Philosophyen

Files

Original bundle
Now showing 1 - 1 of 1
Name:
Carreno_CA_D_2026.pdf
Size:
5.55 MB
Format:
Adobe Portable Document Format