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. 2017 Nov;56(11):922-929.
doi: 10.1016/j.jaac.2017.09.001. Epub 2017 Sep 12.

Thinking Across Generations: Unique Contributions of Maternal Early Life and Prenatal Stress to Infant Physiology

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Thinking Across Generations: Unique Contributions of Maternal Early Life and Prenatal Stress to Infant Physiology

Sarah A O Gray et al. J Am Acad Child Adolesc Psychiatry. 2017 Nov.

Abstract

Objective: Respiratory sinus arrhythmia (RSA) is a parasympathetic-mediated biomarker of self-regulation linked to lifespan mental and physical health outcomes. Intergenerational impacts of mothers' exposure to prenatal stress have been demonstrated, but evidence for biological embedding of maternal preconception stress, including adverse childhood experiences (ACEs), on infant RSA is lacking. We examine the independent effects of maternal ACEs and prenatal stress on infant RSA, seeking to broaden the understanding of the earliest origins of mental and physical health risk.

Method: Mothers reported on ACEs and prenatal stress. RSA was recorded in a sample of 167 4-month-old infants (49% female and 51% male) during a dyadic stressor, the Still Face Paradigm.

Results: Independent contributions of maternal ACEs and prenatal stress to infant RSA were observed. High maternal ACEs were associated with lower RSA, whereas prenatal stress was associated with failure to recover following the stressor. Sex but not race differences were observed. Prenatal stress was associated with higher RSA among boys but lower RSA among girls.

Conclusion: Infants' RSA is affected by mothers' life course experiences of stress, with ACEs predicting a lower set point and prenatal stress dampening recovery from stress. For prenatal stress but not ACEs, patterns vary across sex. Findings underscore that stress-reducing interventions for pregnant women or those considering pregnancy may lead to decreased physical and mental health risk across generations.

Keywords: adverse childhood experiences; prenatal stress; respiratory sinus arrhythmia; still face paradigm; trauma.

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Figures

FIGURE 1
FIGURE 1
Infants with high prenatal stress do not show parasympathetic recovery during still-face reunion; high-stress girls show lower respiratory sinus arrhythmia than low-stress girls, whereas high-stress boys show higher respiratory sinus arrhythmia than low-stress boys. Note: lnRSA = respiratory sinus arrhythmia; PP1 = play period 1; PP2 = play period 2; SEM = standard error of the mean; SF = still face.

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References

    1. Poggi-Davis E, Glynn LM, Waffarn F, Sandman CA. Prenatal maternal stress programs infant stress regulation. J Child Psychol Psychiatry. 2011;52:119–129. - PMC - PubMed
    1. Suurland J, van der Heijden KB, Smaling HJ, Huijbregts SC, van Goozen SH, Swaab H. Infant autonomic nervous system response and recovery: associations with maternal risk status and infant emotion regulation. Dev Psychopathol. 2016;29:1–15. - PubMed
    1. Field T, Diego M, Hernandez-Reif M, et al. Pregnancy anxiety and co-morbid depression and anger: effects on the fetus and neonate. Depress Anxiety. 2003;17:140–151. - PubMed
    1. Peltola MJ, Makela T, Paavonen EJ, et al. Respiratory sinus arrhythmia moderates the impact of maternal prenatal anxiety on infant negative affectivity. Dev Psychobiol. 2017;59:209–216. - PubMed
    1. Cheng ER, Park H, Wisk LE, et al. Examining the link between women’s exposure to stressful life events prior to conception and infant and toddler health: the role of birth weight. J Epidemiol Community Health. 2016;70:245–252. - PMC - PubMed