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Pediatr Res. 2021 Dec;90(6):1186-1192. doi: 10.1038/s41390-021-01381-1. Epub 2021 Feb 18.

Autism risk in neonatal intensive care unit patients associated with novel heart rate patterns.

Pediatric research

Kaitlin R Blackard, Katy N Krahn, Robert T Andris, Douglas E Lake, Karen D Fairchild

Affiliations

  1. Division of Neurodevelopmental and Behavioral Pediatrics, Department of Pediatrics, University of Virginia, Charlottesville, VA, USA. [email protected].
  2. Department of Medicine, University of Virginia, Charlottesville, VA, USA.
  3. Department of Statistics, University of Virginia, Charlottesville, VA, USA.
  4. Division of Neonatology, Department of Pediatrics, University of Virginia, Charlottesville, VA, USA.

PMID: 33603208 PMCID: PMC8371053 DOI: 10.1038/s41390-021-01381-1

Abstract

BACKGROUND: Neonatal intensive care unit (NICU) patients are at increased risk for autism spectrum disorder (ASD). Autonomic nervous system aberrancy has been described in children with ASD, and we aimed to identify heart rate (HR) patterns in NICU patients associated with eventual ASD diagnosis.

METHODS: This retrospective cohort study included NICU patients from 2009 to 2016 with archived HR data and follow-up beyond age 3 years. Medical records provided clinical variables and ASD diagnosis. HR data were compared in infants with and without ASD.

RESULTS: Of the 2371 patients, 88 had ASD, and 689,016 h of data were analyzed. HR skewness (HRskw) was significantly different between ASD and control infants. Preterm infants at early postmenstrual ages (PMAs) had negative HRskw reflecting decelerations, which increased with maturation. From 34 to 42 weeks PMA, positive HRskw toward accelerations was higher in males with ASD. In 931 males with at least 4 days of HR data, overall ASD prevalence was 5%, whereas 11% in the top 5th HRskw percentile had ASD.

CONCLUSION: High HRskw in NICU males, perhaps representing autonomic imbalance, was associated with increased ASD risk. Further study is needed to determine whether HR analysis identifies highest-risk infants who might benefit from earlier screening and therapies.

IMPACT: In a large retrospective single-center cohort of NICU patients, we found that high positive skewness of heart rate toward more accelerations was significantly associated with increased risk of eventual autism spectrum disorder diagnosis in male infants but not in females. Existing literature describes differences in heart rate characteristics in children, adolescents, and adults with autism spectrum disorders, but the finding from our study in NICU infants is novel. Heart rate analysis during the NICU stay might identify, among an inherently high-risk population, those infants with especially high risk of ASD who might benefit from earlier screening and therapies.

© 2021. The Author(s), under exclusive licence to the International Pediatric Research Foundation, Inc.

References

  1. Clin Auton Res. 2016 Dec;26(6):423-432 - PubMed
  2. Infant Child Dev. 2011 Feb;20(1):106-118 - PubMed
  3. J Perinatol. 2019 Jan;39(1):48-53 - PubMed
  4. Front Integr Neurosci. 2019 Nov 19;13:66 - PubMed
  5. J Autism Dev Disord. 2017 Aug;47(8):2434-2442 - PubMed
  6. J Perinatol. 2014 May;34(5):375-9 - PubMed
  7. Eur Child Adolesc Psychiatry. 2006 Jun;15(4):214-9 - PubMed
  8. Res Dev Disabil. 2014 Dec;35(12):3632-44 - PubMed
  9. Pediatr Res. 2016 Jul;80(1):21-7 - PubMed
  10. J Autism Dev Disord. 2015 Feb;45(2):560-75 - PubMed
  11. Dev Psychobiol. 2000 Sep;37(2):73-81 - PubMed
  12. Glia. 2018 Jan;66(1):78-93 - PubMed
  13. Am J Perinatol. 2017 Feb;34(3):295-304 - PubMed
  14. J Dev Behav Pediatr. 2010 Apr;31(3):181-91 - PubMed
  15. Auton Neurosci. 2018 Sep;213:23-33 - PubMed
  16. Early Hum Dev. 1989 Sep;20(1):1-12 - PubMed
  17. Physiol Res. 2016 Dec 22;65(Suppl 5):S673-S682 - PubMed
  18. Biol Psychol. 2019 Mar;142:13-18 - PubMed
  19. Dev Psychopathol. 2013 Nov;25(4 Pt 2):1455-72 - PubMed
  20. Front Integr Neurosci. 2020 Apr 09;14:16 - PubMed
  21. Pediatr Neurol. 2014 Dec;51(6):776-80 - PubMed
  22. J Autism Dev Disord. 2013 Aug;43(8):1910-25 - PubMed
  23. Front Physiol. 2018 May 01;9:467 - PubMed
  24. Brain Dev. 2016 Feb;38(2):225-32 - PubMed
  25. Early Hum Dev. 2019 Oct;137:104817 - PubMed
  26. Front Neurosci. 2013 Jul 22;7:123 - PubMed
  27. Am J Perinatol. 2018 Nov;35(13):1331-1338 - PubMed
  28. J Autism Dev Disord. 2015 Feb;45(2):461-72 - PubMed
  29. Am J Perinatol. 2014 Nov;31(10):855-62 - PubMed
  30. Circulation. 2012 Aug 28;126(9):1143-72 - PubMed
  31. Auton Neurosci. 2012 Nov 2;171(1-2):4-7 - PubMed
  32. J Clin Child Adolesc Psychol. 2008 Jan;37(1):8-38 - PubMed
  33. PLoS One. 2018 Jul 17;13(7):e0200799 - PubMed
  34. Pediatrics. 2006 Jul;118(1):309-21 - PubMed
  35. BMC Pediatr. 2019 May 8;19(1):144 - PubMed
  36. JAMA. 2015 Apr 14;313(14):1425-34 - PubMed
  37. Pediatr Res. 2017 Feb;81(2):315-321 - PubMed
  38. Biol Psychiatry. 2017 Aug 1;82(3):155-156 - PubMed

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