Sex-dimorphic pathways in the associations between maternal trait anxiety, infant BDNF methylation, and negative emotionality.

Autor: Nazzari S; Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy., Grumi S; Developmental Psychobiology Lab, IRCCS Mondino Foundation, Pavia, Italy., Mambretti F; Molecular Biology Lab, Scientific Institute IRCCS E. Medea, Bosisio Parini, Italy., Villa M; Molecular Biology Lab, Scientific Institute IRCCS E. Medea, Bosisio Parini, Italy., Giorda R; Molecular Biology Lab, Scientific Institute IRCCS E. Medea, Bosisio Parini, Italy., Bordoni M; Cellular Models and Neuroepigenetics Unit, IRCCS Mondino Foundation, Pavia, Italy., Pansarasa O; Cellular Models and Neuroepigenetics Unit, IRCCS Mondino Foundation, Pavia, Italy., Borgatti R; Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.; Developmental Psychobiology Lab, IRCCS Mondino Foundation, Pavia, Italy., Provenzi L; Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.; Developmental Psychobiology Lab, IRCCS Mondino Foundation, Pavia, Italy.
Jazyk: angličtina
Zdroj: Development and psychopathology [Dev Psychopathol] 2024 May; Vol. 36 (2), pp. 908-918. Date of Electronic Publication: 2023 Mar 01.
DOI: 10.1017/S0954579423000172
Abstrakt: Maternal antenatal anxiety is an emerging risk factor for child emotional development. Both sex and epigenetic mechanisms, such as DNA methylation, may contribute to the embedding of maternal distress into emotional outcomes. Here, we investigated sex-dependent patterns in the association between antenatal maternal trait anxiety, methylation of the brain-derived neurotrophic factor gene ( BDNF DNAm ), and infant negative emotionality (NE). Mother-infant dyads ( N = 276) were recruited at delivery. Maternal trait anxiety, as a marker of antenatal chronic stress exposure, was assessed soon after delivery using the Stait-Trait Anxiety Inventory (STAI-Y). Infants' BDNF DNAm at birth was assessed in 11 CpG sites in buccal cells whereas infants' NE was assessed at 3 ( N = 225) and 6 months ( N = 189) using the Infant Behavior Questionnaire-Revised (IBQ-R). Hierarchical linear analyses showed that higher maternal antenatal anxiety was associated with greater 6-month-olds' NE. Furthermore, maternal antenatal anxiety predicted greater infants' BDNF DNAm in five CpG sites in males but not in females. Higher methylation at these sites was associated with greater 3-to-6-month NE increase, independently of infants' sex. Maternal antenatal anxiety emerged as a risk factor for infant's NE. BDNF DNAm might mediate this effect in males. These results may inform the development of strategies to promote mothers and infants' emotional well-being.
Databáze: MEDLINE