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Patterns of fetal heart rate response at ∼30 weeks gestation predict size at birth

Published online by Cambridge University Press:  13 June 2011

C. A. Sandman*
Affiliation:
Women and Children's Health and Well-Being Project, Department of Psychiatry and Human Behavior, University of California, Irvine, Orange, CA, USA
C. J. Cordova
Affiliation:
Women and Children's Health and Well-Being Project, Department of Psychiatry and Human Behavior, University of California, Irvine, Orange, CA, USA
E. P. Davis
Affiliation:
Women and Children's Health and Well-Being Project, Department of Psychiatry and Human Behavior, University of California, Irvine, Orange, CA, USA Department of Pediatrics, University of California, Irvine, CA, USA
L. M. Glynn
Affiliation:
Women and Children's Health and Well-Being Project, Department of Psychiatry and Human Behavior, University of California, Irvine, Orange, CA, USA Crean School of Health and Life Sciences, Chapman University, Orange, CA, USA
C. Buss
Affiliation:
Women and Children's Health and Well-Being Project, Department of Psychiatry and Human Behavior, University of California, Irvine, Orange, CA, USA Department of Pediatrics, University of California, Irvine, CA, USA
*
*Address for correspondence: C. A. Sandman, Women and Children's Health and Well-Being Project, Department of Psychiatry and Human Behavior, University of California, 333 City Drive, Suite 1200, Orange, CA 92868-3205, USA. (Email [email protected])

Abstract

There is evidence that fetal exposure to maternal stress is associated with adverse birth outcomes. Less is known about the association between fetal responses to a stressor and indicators of fetal maturity and developmental outcomes. The purpose of the present study was to determine whether fetal heart rate (FHR) patterns in response to a startling stimulus at ∼30 weeks of gestation were associated with gestational age at birth and birth weight. FHR was measured in 156 maternal–fetal dyads following a vibroacoustic stimulus. All pregnancies were singleton intrauterine pregnancies in English-speaking women who were primarily married, middle class, White and at least 18 years of age. Group-based trajectory modeling identified five groups of fetuses displaying distinctive longitudinal trajectories of FHR response to the startling stimulus. The FHR group trajectories were significantly associated with birth weight percentile (P < 0.01) even after controlling for estimated fetal weight at the time of assessment and parity, which are the known factors influencing birth weight (P < 0.01). Post hoc analyses indicated that two groups accounted for the association between FHR patterns and birth weight. The group (n = 23) with the lowest birth weight exhibited an immediate FHR deceleration followed by an immediate acceleration that does not recover. An FHR pattern characterized by immediate and fast acceleration to the peak and a slow discovery to baseline was associated with the highest birth weight. This is the first direct evidence showing that low birth weight and the resulting neurological consequences may have their origins in early fetal development.

Type
Original Articles
Copyright
Copyright © Cambridge University Press and the International Society for Developmental Origins of Health and Disease 2011

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References

1.Barker, DJP. Mothers, Babies and Health in Later Life, 1998. Churchill Livingston: Edinburgh.Google Scholar
2.Barker, DJ, Osmond, C, Simmonds, SJ, Wield, GA. The relation of small head circumference and thinness at birth to death from cardiovascular disease in adult life. BMJ. 1993; 306, 422426.Google Scholar
3.McCormack, VA, Silva, I, De Stavola, BL, et al. Fetal growth and subsequent risk of breast cancer: results from long term follow up of Swedish cohort. BMJ. 2003; 326, 248.CrossRefGoogle ScholarPubMed
4.Roseboom, TJ, van der Meulen, JHP, Osmond, C, et al. Coronary heart disease after prenatal exposure to the Dutch famine, 1944–45. Heart. 2000; 84, 595598.CrossRefGoogle Scholar
5.Richards, M, Hardy, R, Kuh, D, Wadsworth, ME. Birth weight and cognitive function in the British 1946 birth cohort: longitudinal population based study. BMJ. 2001; 322, 199203.Google Scholar
6.Sandman, CA, Davis, EP. Gestational stress influences cognition and behavior. Future Neurol. 2010; 5, 675690.CrossRefGoogle Scholar
7.Glynn, LM, Wadhwa, PD, Dunkel-Schetter, C, Chicz-Demet, A, Sandman, CA. When stress happens matters: effects of earthquake timing on stress responsivity in pregnancy. Am J Obstet Gynecol. 2001; 184, 637642.Google Scholar
8.Rini, CK, Dunkel-Schetter, C, Wadhwa, PD, Sandman, CA. Psychological adaptation and birth outcomes: the role of personal resources, stress, and sociocultural context in pregnancy. Health Psychol. 1999; 18, 333345.CrossRefGoogle ScholarPubMed
9.Wadhwa, PD, Sandman, CA, Porto, M, Dunkel-Schetter, C, Garite, TJ. The association between prenatal stress and infant birth weight and gestational age at birth: a prospective investigation. Am J Obstet Gynecol. 1993; 169, 858865.Google Scholar
10.Vlastos, EJ, Tomlinson, TM, Bildirici, I, et al. Fetal heart rate accelerations and the risk of cerebral lesions and poor neurodevelopmental outcome in very low birthweight neonates. Am J Perinatol. 2007; 24, 8388.Google Scholar
11.Almli, CR, Ball, RH, Wheeler, ME. Human fetal and neonatal movement patterns: gender differences and fetal-to-neonatal continuity. Dev Psychobiol. 2001; 38, 252273.CrossRefGoogle ScholarPubMed
12.Groome, LJ, Swiber, MJ, Holland, SB, et al. Spontaneous motor activity in the perinatal infant before and after birth: stability in individual differences. Dev Psychobiol. 1999; 35, 1524.Google Scholar
13.Leader, LR, Baillie, P, Martin, B, Vermeulen, E. The assessment and significance of habituation to a repeated stimulus by the human fetus. Early Hum Dev. 1982; 7, 211219.CrossRefGoogle ScholarPubMed
14.DiPietro, JA, Bornstein, MH, Hahn, CS, Costigan, K, Achy-Brou, A. Fetal heart rate and variability: stability and prediction to developmental outcomes in early childhood. Child Dev. 2007; 78, 17881798.Google Scholar
15.Werner, EA, Myers, MM, Fifer, WP, et al. Prenatal predictors of infant temperament. Dev Psychobiol. 2007; 49, 474484.Google Scholar
16.DiPietro, JA, Hodgson, DM, Costigan, KA, Johnson, TR. Fetal antecedents of infant temperament. Child Dev. 1996; 67, 25682583.CrossRefGoogle ScholarPubMed
17.DiPietro, JA, Bornstein, MH, Costigan, KA, et al. What does fetal movement predict about behavior during the first two years of life? Dev Psychobiol. 2002; 40, 358371.CrossRefGoogle ScholarPubMed
18.DiPietro, JA, Costigan, KA, Pressman, EK. Fetal state concordance predicts infant state regulation. Early Hum Dev. 2002; 68, 113.CrossRefGoogle ScholarPubMed
19.DiPietro, JA, Costigan, KA, Pressman, EK, Doussard-Roosevelt, JA. Antenatal origins of individual differences in heart rate. Dev Psychobiol. 2000; 37, 221228.3.0.CO;2-A>CrossRefGoogle ScholarPubMed
20.Kisilevsky, BS, Muir, DW. Human fetal and subsequent newborn responses to sound and vibration. Infant Behav Dev. 1991; 14, 126.CrossRefGoogle Scholar
21.Gagnon, R, Hunse, C, Patrick, J. Fetal responses to vibratory acoustic stimulation: influence of basal heart rate. Am J Obstet Gynecol. 1988; 159, 835839.Google Scholar
22.Gagnon, R, Campbell, K, Hunse, C, Patrick, J. Patterns of human fetal heart rate accelerations from 26 weeks to term. Am J Obstet Gynecol. 1987; 157, 743748.Google Scholar
23.Gagnon, R, Hunse, C, Fellows, F, Carmichael, L, Patrick, J. Fetal heart rate and activity patterns in growth-retarded fetuses: changes after vibratory acoustic stimulation. Am J Obstet Gynecol. 1988; 158, 265271.Google Scholar
24.Gagnon, R, Patrick, J, Foreman, J, West, R. Stimulation of human fetuses with sound and vibration. Am J Obstet Gynecol. 1986; 155, 848851.Google Scholar
25.Lecanuet, JP, Granier-Deferre, C, Busnel, MC. Fetal cardiac and motor responses to octave-band noises as a function of central frequency, intensity and heart rate variability. Early Hum Dev. 1988; 18, 8193.Google Scholar
26.Pietrantoni, M, Angel, JL, Parsons, MT, et al. Human fetal response to vibroacoustic stimulation as a function of stimulus duration. Obstet Gynecol. 1991; 78, 807811.Google ScholarPubMed
27.Leader, LR, Baillie, P, Martin, B, Vermeulen, E. Fetal habituation in high-risk pregnancies. Br J Obstet Gynaecol. 1982; 89, 441446.Google Scholar
28.Shalev, E, Benett, MJ, Megory, E, Wallace, RM, Zuckerman, H. Fetal habituation to repeated sound stimulation. Isr J Med Sci. 1989; 25, 7780.Google Scholar
29.Zimmer, EZ, Chao, CR, Guy, GP, Marks, F, Fifer, WP. Vibroacoustic stimulation evokes human fetal micturition. Obstet Gynecol. 1993; 81, 178180.Google Scholar
30.Grimwade, JC, Walker, DW, Bartlett, M, Gordon, S, Wood, C. Human fetal heart rate change and movement in response to sound and vibration. Am J Obstet Gynecol. 1971; 109, 8690.CrossRefGoogle ScholarPubMed
31.DeCasper, AJ, Fifer, WP. Of human bonding: newborns prefer their mothers’ voices. Science. 1980; 208, 11741176.Google Scholar
32.Fifer, WP, Moon, C. Psychobiology of newborn auditory preferences. Semin Perinatol. 1989; 13, 430433.Google ScholarPubMed
33.Sandman, CA, Wadhwa, P, Hetrick, W, Porto, M, Peeke, HV. Human fetal heart rate dishabituation between thirty and thirty-two weeks gestation. Child Dev. 1997; 68, 10311040.CrossRefGoogle ScholarPubMed
34.Buss, C, Davis, EP, Class, QA, et al. Maturation of the human fetal startle response: evidence for sex-specific maturation of the human fetus. Early Hum Dev. 2009; 85, 633638.CrossRefGoogle ScholarPubMed
35.Class, QA, Buss, C, Davis, EP, et al. Low levels of corticotropin-releasing hormone during early pregnancy are associated with precocious maturation of the human fetus. Dev Neurosci. 2008; 30, 419426.Google Scholar
36.Oken, E, Kleinman, KP, Rich-Edwards, J, Gillman, MW. A nearly continuous measure of birth weight for gestational age using a United States national reference. BMC Pediatr. 2003; 3, 6.Google Scholar
37.American College of Obstetricians and Gynecologists (ACOG). Practice Bulletin No. 101: Ultrasonography in pregnancy. Obstet Gynecol. 2009; 113, 451461.Google Scholar
38.Hadlock, FP, Harrist, RB, Sharman, RS, Deter, RL, Park, SK. Estimation of fetal weight with the use of head, body, and femur measurements – a prospective study. Am J Obstet Gynecol. 1985; 151, 333337.CrossRefGoogle ScholarPubMed
39.Nagin, DS. Group-based Modeling of Development, 2005. Harvard University Press: Cambridge, MA.Google Scholar
40.Glynn, LM, Schetter, CD, Hobel, CJ, Sandman, CA. Pattern of perceived stress and anxiety in pregnancy predicts preterm birth. Health Psychol. 2008; 27, 4351.CrossRefGoogle ScholarPubMed
41.Dunkel Schetter, C. Stress processes in pregnancy and preterm birth. Curr Dir Psychol Sci. 2009; 18, 204209.Google Scholar
42.Dunkel Schetter, C, Glynn, LM. Stress in pregnancy: empirical evidence and theoretical issues to guide interdisciplinary research. In Handbook of Stress (eds. Contrada R, Baum A), 2010, pp. 321343. Springer: New York.Google Scholar
43.Van den Bergh, B. The influence of maternal emotions during pregnancy on fetal and neonatal behavior. Pre- Peri-Nat Psychol J. 1990; 5, 119130.Google Scholar
44.Davis, EP, Sandman, CA. The timing of prenatal exposure to maternal cortisol and psychosocial stress is associated with human infant cognitive development. Child Dev. 2010; 81, 131148.Google Scholar
45.Buss, C, Davis, EP, Muftuler, LT, Head, K, Sandman, CA. High pregnancy anxiety during mid-gestation is associated with decreased gray matter density in 6-9-year-old children. Psychoneuroendocrinology. 2010; 35, 141153.CrossRefGoogle ScholarPubMed
46.Ellman, LM, Dunkel Schetter, C, Hobel, CJ, et al. Timing of fetal exposure to stress hormones: effects on newborn physical and neuromuscular maturation. Dev Psychobiol. 2008; 50, 232241.CrossRefGoogle ScholarPubMed
47.Dipietro, JA, Irizarry, RA, Hawkins, M, Costigan, KA, Pressman, EK. Cross-correlation of fetal cardiac and somatic activity as an indicator of antenatal neural development. Am J Obstet Gynecol. 2001; 185, 14211428.Google Scholar
48.Hepper, PG. The behavior of the fetus as an indicator of neural functioning. In Fetal Development: A Psychobiological Perspective (eds. Lecanuet J-P, Fifer WP, Krasnegor NA, Smotherman WP), 1995, pp. 405417. Lawrence Erlbaum Associates: Hillsdale.Google Scholar
49.Nijhuis, IJ, ten Hof, J, Nijhuis, JG, et al. Temporal organization of fetal behavior from 24-weeks gestation onwards in normal and complicated pregnancies. Dev Psychobiol. 1999; 34, 257268.Google Scholar
50.Nijhuis, JG. Fetal behavior. Neurobiol Aging. 2003; 24 (Suppl 1), S41S46.Google Scholar
51.Lundgren, EMT, Tuvemo, T. Effects of being born small for gestational age on long-term intellectual performance. Best Pract Res Clin Endocrinol Metab. 2008; 22, 477488.Google Scholar