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Maternal verbally aggressive behavior in early infancy is associated with blood pressure at age 5–6

Published online by Cambridge University Press:  01 February 2018

L. J. C. A. Smarius*
Affiliation:
Department of Public Health, Amsterdam Public Health Research Institute, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands Academic Center for Child and Adolescent Psychiatry de Bascule, Amsterdam, The Netherlands Department of Child and Adolescent Psychiatry, VU University Medical Center, AmsterdamThe Netherlands
T. G. A. Strieder
Affiliation:
Arkin Institute for Mental Health, Amsterdam, The Netherlands
T. A. H. Doreleijers
Affiliation:
Department of Child and Adolescent Psychiatry, VU University Medical Center, AmsterdamThe Netherlands
T. G. M. Vrijkotte
Affiliation:
Department of Public Health, Amsterdam Public Health Research Institute, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands
S. R. de Rooij
Affiliation:
Department of Public Health, Amsterdam Public Health Research Institute, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands Department of Clinical Epidemiology, Biostatistics and Bio-informatics, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands
*
*Address for correspondence: L. J. C. A. Smarius, Department of Public Health, Academic Medical Center, University of Amsterdam, Postbus 22660, 1100 DD Amsterdam, The Netherlands. E-mail: [email protected]

Abstract

Early life stress has been shown to contribute to alterations in biobehavioral regulation. Whereas many different forms of childhood adversities have been studied in relation to cardiovascular outcomes, very little is known about potential associations between caregivers’ verbally aggressive behavior and heart rate and blood pressure in the child. This prospective study examined whether maternal verbally aggressive behavior in early infancy is associated with heart rate or blood pressure at age 5–6. In the Amsterdam Born Children and their Development study, a large prospective, population-based birth cohort, maternal verbally aggressive behavior was assessed by questionnaire in the 13th week after birth. The child’s blood pressure and heart rate were measured during rest at age 5–6 (n=2553 included). Maternal verbally aggressive behavior in infancy was associated with a higher systolic blood pressure (SBP) both in supine and sitting position after adjustment for sex, height and age (SBP supine B=1.01 mmHg; 95% CI [0.06; 1.95] and SPB sitting B=1.29 mmHg; 95% CI [0.12; 2.46]). Adjustment for potential confounding variables, such as other mother–infant dyad aspects, family hypertension and child’s BMI, only slightly attenuated the associations (SBP supine B=0.99 mmHg; 95% CI [0.06; 1.93] and SPB sitting B=1.11 mmHg; 95% CI [−0.06; 2.27]). Maternal verbally aggressive behavior was not associated with diastolic blood pressure or heart rate at age 5–6. Maternal verbally aggressive behavior might be an important early life stressor with negative impact on blood pressure later in life, which should be further investigated. Possible underlying mechanisms are discussed.

Type
Original Article
Copyright
© Cambridge University Press and the International Society for Developmental Origins of Health and Disease 2018 

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References

1. Loria, AS, Ho, DH, Pollock, JS. A mechanistic look at the effects of adversity early in life on cardiovascular disease risk during adulthood. Acta Physiol (Oxf). 2014; 210, 277287.CrossRefGoogle Scholar
2. Murphy, MO, Cohn, DM, Loria, AS. Developmental origins of cardiovascular disease: Impact of early life stress in humans and rodents. Neurosci Biobehav Rev. 2017; 74, 453465.Google Scholar
3. Theodore, AD, Chang, JJ, Runyan, DK, et al. Epidemiologic features of the physical and sexual maltreatment of children in the Carolinas. Pediatrics. 2005; 115, e331e337.CrossRefGoogle ScholarPubMed
4. Parrish, C, Surkan, PJ, Martins, SS, et al. Childhood adversity and adult onset of hypertension and heart disease in São Paulo, Brazil. Prev Chronic Dis. 2013; 10, E205.Google Scholar
5. Slopen, N, Non, A, Williams, DR, Roberts, AL, Albert, MA. Childhood adversity, adult neighborhood context, and cumulative biological risk for chronic diseases in adulthood. Psychosom Med. 2014; 76, 481489.Google Scholar
6. Su, S, Wang, X, Pollock, JS, et al. Adverse childhood experiences and blood pressure trajectories from childhood to young adulthood: the Georgia stress and Heart study. Circulation. 2015; 131, 16741681.Google Scholar
7. Pretty, C, O’Leary, DD, Cairney, J, Wade, TJ. Adverse childhood experiences and the cardiovascular health of children: a cross-sectional study. BMC Pediatr. 2013; 17, 208.Google Scholar
8. Lambregtse-van den Berg, MP, Lucassen, N, Kuipers-Nap, MF, et al. Assessing expressed emotion during pregnancy. Psychiatry Res. 2013; 205, 285288.Google Scholar
9. Seltzer, LJ, Ziegler, TE, Pollak, SD. Social vocalizations can release oxytocin in humans. Procedings. Biological Sciences. 2010; 277, 26612666.Google ScholarPubMed
10. MacLean, PC, Rynes, KN, Aragón, C, et al. Mother-infant mutual eye gaze supports emotion regulation in infancy during the Still-Face paradigm. Infant Behav Dev. 2014; 37, 512522.CrossRefGoogle ScholarPubMed
11. Naughton, AM, Maguire, SA, Mann, MK, et al. Emotional, behavioral, and developmental features indicative of neglect or emotional abuse in preschool children: a systematic review. JAMA Pediatr. 2013; 167, 769775.CrossRefGoogle ScholarPubMed
12. Brummelte, S, Galea, LA. Postpartum depression: etiology, treatment and consequences for maternal care. Horm Behav. 2016; 77, 153166.Google Scholar
13. Dollberg, D, Feldman, R, Keren, M. Maternal representations, infant psychiatric status, and mother-child relationship in clinic-referred and non-referred infants. Eur Child Adolesc Psychiatry. 2010; 19, 2536.Google Scholar
14. Van Eijsden, E, Vrijkotte, TGM, Gemke, RJBJ, van der Wal, MF. Cohort profile: The Amsterdam Born Children and their Development (ABCD) study. Int J Epidemiol. 2011; 40, 11761186.CrossRefGoogle ScholarPubMed
15. de Geus, EJ, Willemsen, GH, Klaver, CH, van Doornen, LJ. Ambulatory measurement of respiratory sinus arrhythmia and respiration rate. Biol Psychol. 1995; 41, 205227.Google Scholar
16. Van Dijk, AE, van Lien, R, van Eijsden, M, et al. Measuring cardiac autonomic nervous system (ANS) activity in children. J Vis Exp. 2013; 74, e50073.Google Scholar
17. Van der Wal, MF, van Eijsden, M, Bonsel, GJ. Stress and emotional problems during pregnancy and excessive infant crying. J Dev Behav Paediatr. 2007; 28, 431437.CrossRefGoogle ScholarPubMed
18. Smarius, LJ, Strieder, TG, Loomans, EM, et al. Excessive infant crying doubles the risk of mood and behavioral problems at age 5: evidence for mediation by maternal characteristics. Eur Child Adolesc Psychiatry. 2017; 26, 293302.Google Scholar
19. Knight, RG, Williams, S, McGee, R, Olaman, S. Psychometric properties of the Centre for Epidemiologic Studies Depression Scale (CES-D) in a sample of women in middle life. Behav Res Ther. 1997; 35, 373380.Google Scholar
20. van Dijk, A E, van Eijsden, M, Stronks, K, Gemke, R J, Vrijkotte, TG. The association between prenatal psychosocial stress and blood pressure in the child at age 5-7 years. PLoS One. 2012; 7, e43548.Google Scholar
21. Robinson, CC, Mandleco, B, Olsen, SF, Hart, CH. The Parenting Styles and Dimensions Questionnaire (PSDQ). In: Handbook of Family Measurement Techniques (eds. Perlmutter BF, Touliatos J, Holden GW), 2001; pp. 319321. Sage: Thousand Oaks.Google Scholar
22. de Brock, AJ, Vermulst, AA, Gerris, JR, Abidin, RR. NOSI, handleiding experimentele versie [NOSI, manual experimental version in Dutch]/Parenting Stress Index. 1992. Pearson: Amsterdam.Google Scholar
23. Henry, JD, Crawford, JR. The short-form version of the Depression Anxiety Stress Scales (DASS-21): construct validity and normative data in a large non-clinical sample. Br J Clin Psychol. 2005; 44, 227239.CrossRefGoogle Scholar
24. Gooding, HC, Milliren, CE, Austin, SB, Sheridan, MA, McLaughlin, KA. Child abuse, resting blood pressure, and blood pressure reactivity to psychosocial stress. J Pediatr Psychol. 2016; 41, 514.CrossRefGoogle ScholarPubMed
25. Chen, X, Wang, Y. Tracking of blood pressure from childhood to adulthood: a systematic review and meta-regression analysis. Circulation. 2008; 117, 31713180.Google Scholar
26. Toschke, AM, Kohl, L, Mansmann, U, von Kries, R. Meta-analysis of blood pressure tracking from childhood to adulthood and implications for the design of intervention trials. Acta Paediatr. 2010; 99, 2429.CrossRefGoogle ScholarPubMed
27. Galea, S, Tracy, M. Participation rates in epidemiological studies. Ann Epidemiol. 2007; 17, 643653.Google Scholar
28. Johansson, S, Norman, M, Legnevall, L, et al. Increased catecholamines and heart rate in children with low birth weight: perinatal contributions to sympathoadrenal overactivity. J Intern Med. 2007; 261, 480487.Google Scholar
29. Cassidy, J, Mohr, JJ. Unsolvable fear, trauma and psychopathology; theory, research and clinical considerations related to disorganized attachment across the live cycle. Clin Psychol. 2001; 8, 275298.Google Scholar
30. Liotti, G. Trauma, dissociation and disorganized attachment: three stands of a single braid. Psychotherapy. 2004; 41, 472486.CrossRefGoogle Scholar
31. Schore, AN. Affect Dysregulation and the Disorders of the Self. 2003. Norton: New York.Google Scholar
32. Pesonen, AK, Räikkönen, K, Feldt, K, et al. Childhood separation experience predicts HPA axis hormonal responses in late adulthood: a natural experiment of World War II. Psychoneuroendocrinology. 2010; 35, 758767.Google Scholar
33. Danese, A, McEwen, BS. Adverse childhood experiences, allostasis, allostatic load, and age-related disease. Physiol Behav. 2012; 106, 2939.Google Scholar
34. Pervanidou, P, Chrousos, GP. Metabolic consequences of stress during childhood and adolescence. Metabolism. 2012; 61, 611619.Google Scholar
35. Boyne, MS, Woollard, A, Phillips, DI, et al. The association of hypothalamic-pituitary-adrenal axis activity and blood pressure in an Afro-Caribbean population. Psychoneuroendocrinology. 2009; 34, 736742.Google Scholar
36. Krishnaveni, GV, Veena, SR, Dhube, A, et al. Size at birth, morning cortisol and cardiometabolic risk markers in healthy Indian children. Clin Endocrinol (Oxf). 2014; 80, 7379.Google Scholar
37. Nuyt, AM, Alexander, BT. Developmental programming and hypertension. Curr Opin Nephrol Hypertens. 2009; 18, 144152.Google Scholar
38. Fan, Y, Herrera-Melendez, AL, Pestke, K, et al. Early life stress modulates amygdala-prefrontal functional connectivity: implications for oxytocin effects. Hum Brain Mapp. 2014; 35, 53285339.CrossRefGoogle ScholarPubMed
39. Shin, LM, Wright, CI, Cannistraro, PA, et al. A functional magnetic resonance imaging study of amygdala and medial prefrontal cortex responses to overtly presented fearful faces in posttraumatic stress disorder. Arch Gen Psychiatry. 2005; 62, 273281.CrossRefGoogle ScholarPubMed
40. Bremner, JD, Vermetten, E, Schmahl, C, et al. Positron emission tomographic imaging of neural correlates of a fear acquisition and extinction paradigm in women with childhood sexual-abuse-related post-traumatic stress disorder. Psychol Med. 2005; 35, 791806.Google Scholar
41. Tawakol, A, Ishai, A, Takx, RA, et al. Relation between resting amygdalar activity and cardiovascular events: a longitudinal and cohort study. Lancet. 2017; 389, 834845.CrossRefGoogle ScholarPubMed