Eur J Pediatr Surg 2023; 33(01): 011-016
DOI: 10.1055/a-1905-4808
Original Article

Seasonal Variation of Congenital Diaphragmatic Hernia: A Review of the Literature and Database Report from the United States and Canada

Fabian Doktor
1   Developmental and Stem Cell Biology Program, Peter Gilgan Centre for Research and Learning, The Hospital for Sick Children, Toronto, Ontario, Canada
2   Division of General and Thoracic Surgery, The Hospital for Sick Children, Toronto, Ontario, Canada
,
Lina Antounians
1   Developmental and Stem Cell Biology Program, Peter Gilgan Centre for Research and Learning, The Hospital for Sick Children, Toronto, Ontario, Canada
2   Division of General and Thoracic Surgery, The Hospital for Sick Children, Toronto, Ontario, Canada
,
Jason Miller
3   CDH Patient Registry, CDH International, Wake Forest, North Carolina, United States
,
Maria Harb
3   CDH Patient Registry, CDH International, Wake Forest, North Carolina, United States
,
Tracy Meats
3   CDH Patient Registry, CDH International, Wake Forest, North Carolina, United States
,
Rachel Bercovitch
1   Developmental and Stem Cell Biology Program, Peter Gilgan Centre for Research and Learning, The Hospital for Sick Children, Toronto, Ontario, Canada
2   Division of General and Thoracic Surgery, The Hospital for Sick Children, Toronto, Ontario, Canada
,
3   CDH Patient Registry, CDH International, Wake Forest, North Carolina, United States
,
Augusto Zani
1   Developmental and Stem Cell Biology Program, Peter Gilgan Centre for Research and Learning, The Hospital for Sick Children, Toronto, Ontario, Canada
2   Division of General and Thoracic Surgery, The Hospital for Sick Children, Toronto, Ontario, Canada
4   Department of Surgery, University of Toronto, Toronto, Ontario, Canada
› Author Affiliations
Funding This study was funded by the SickKids Foundation, CDH Fund: R00DH00000.

Abstract

Introduction The etiology of congenital diaphragmatic hernia (CDH) remains unknown and only 10 to 30% of patients have a genetic cause. Seasonal variation is known to contribute to the development of some congenital anomalies. Our aim was to investigate whether CDH births have seasonal variation.

Materials and Methods A literature review was conducted for CDH and seasonality. Moreover, data from the CDH International Patient Registry Database were collected for infants with due dates between 2008 and 2014. Due dates were used to determine seasonal distribution of births. Birth rates per month in the United States and Canada were extracted from publicly available databases. Data were analyzed using analysis of variance and contingency tables.

Results First, the literature review revealed 11 articles, of which 3 were eligible for inclusion. These studies reported conflicting results on seasonality of CDH. Second, we extracted due dates from the CDH International Patient Registry Database (1,259 patients) and found that there were fewer due dates in winter months (12.1 ± 4 patients/month) than in summer (16.7 ± 6 patients/month; p = 0.011) and fall months (16.3 ± 5 patients/month; p = 0.022). Although this trend was similar to that of all births in the United States and Canada, a lower incidence was observed in winter for CDH infants (20.2%) than for the general population (24.1%, p = 0.0012). CDH survival rate did not vary by season.

Conclusion This study provides evidence for a seasonal variation of CDH births. No causative link was established between CDH development and seasonality. Population-based studies with a focus on exposome data are needed to explain seasonal variation in CDH.



Publication History

Received: 03 June 2022

Accepted: 18 July 2022

Accepted Manuscript online:
20 July 2022

Article published online:
26 December 2022

© 2022. Thieme. All rights reserved.

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Rüdigerstraße 14, 70469 Stuttgart, Germany

 
  • References

  • 1 Paoletti M, Raffler G, Gaffi MS, Antounians L, Lauriti G, Zani A. Prevalence and risk factors for congenital diaphragmatic hernia: a global view. J Pediatr Surg 2020; 55 (11) 2297-2307
  • 2 Zani A, Chung WK, Deprest J. et al. Congenital diaphragmatic hernia. Nat Rev Dis Primers 2022; 8 (01) 37
  • 3 Donahoe PK, Longoni M, High FA. Polygenic causes of congenital diaphragmatic hernia produce common lung pathologies. Am J Pathol 2016; 186 (10) 2532-2543
  • 4 Wynn J, Yu L, Chung WK. Genetic causes of congenital diaphragmatic hernia. Semin Fetal Neonatal Med 2014; 19 (06) 324-330
  • 5 Enns GM, Cox VA, Goldstein RB, Gibbs DL, Harrison MR, Golabi M. Congenital diaphragmatic defects and associated syndromes, malformations, and chromosome anomalies: a retrospective study of 60 patients and literature review. Am J Med Genet 1998; 79 (03) 215-225
  • 6 Longoni M, High FA, Qi H. et al. Genome-wide enrichment of damaging de novo variants in patients with isolated and complex congenital diaphragmatic hernia. Hum Genet 2017; 136 (06) 679-691
  • 7 Schulz F, Jenetzky E, Zwink N. et al. Parental risk factors for congenital diaphragmatic hernia - a large German case-control study. BMC Pediatr 2021; 21 (01) 278
  • 8 Inderbinen SG, Kley M, Zogg M. et al. Activation of retinoic acid-related orphan receptor γ(t) by parabens and benzophenone UV-filters. Toxicology 2022; 471: 153159
  • 9 Beurskens N, Klaassens M, Rottier R, de Klein A, Tibboel D. Linking animal models to human congenital diaphragmatic hernia. Birth Defects Res A Clin Mol Teratol 2007; 79 (08) 565-572
  • 10 Antounians L, Figueira RL, Sbragia L, Zani A. Congenital diaphragmatic hernia: state of the art in translating experimental research to the bedside. Eur J Pediatr Surg 2019; 29 (04) 317-327
  • 11 Kool HM, Bürgisser PE, Edel GG. et al. Inhibition of retinoic acid signaling induces aberrant pericyte coverage and differentiation resulting in vascular defects in congenital diaphragmatic hernia. Am J Physiol Lung Cell Mol Physiol 2019; 317 (03) L317-L331
  • 12 Clugston RD, Zhang W, Alvarez S, de Lera AR, Greer JJ. Understanding abnormal retinoid signaling as a causative mechanism in congenital diaphragmatic hernia. Am J Respir Cell Mol Biol 2010; 42 (03) 276-285
  • 13 Auriti C, De Rose DU, Santisi A. et al. Pregnancy and viral infections: mechanisms of fetal damage, diagnosis and prevention of neonatal adverse outcomes from cytomegalovirus to SARS-CoV-2 and Zika virus. Biochim Biophys Acta Mol Basis Dis 2021; 1867 (10) 166198
  • 14 Ye Z, Wang L, Yang T. et al. Maternal viral infection and risk of fetal congenital heart diseases: a meta-analysis of observational studies. J Am Heart Assoc 2019; 8 (09) e0112644
  • 15 Czeizel AE, Puhó EH, Acs N, Bánhidy F. Use of specified critical periods of different congenital abnormalities instead of the first trimester concept. Birth Defects Res A Clin Mol Teratol 2008; 82 (03) 139-146
  • 16 Bound JP, Harvey PW, Francis BJ. Seasonal prevalence of major congenital malformations in the Fylde of Lancashire 1957-1981. J Epidemiol Community Health 1989; 43 (04) 330-342
  • 17 Luteijn JM, Brown MJ, Dolk H. Influenza and congenital anomalies: a systematic review and meta-analysis. Hum Reprod 2014; 29 (04) 809-823
  • 18 Loder RT, Shafer C. Seasonal variation in children with developmental dysplasia of the hip. J Child Orthop 2014; 8 (01) 11-22
  • 19 Martin JA, Hamilton BE, Sutton PD, Ventura SJ, Mathews TJ, Osterman MJK. Births: final data for 2008. Natl Vital Stat Rep 2010; 59 (01) 1 , 3–71
  • 20 Martin JA, Hamilton BE, Ventura SJ. et al. Births: final data for 2009. Natl Vital Stat Rep 2011; 60 (01) 1-70
  • 21 Martin JA, Hamilton BE, Ventura SJ, Osterman MJK, Wilson EC, Mathews TJ. Births: final data for 2010. Natl Vital Stat Rep 2012; 61 (01) 1-72
  • 22 Martin JA, Hamilton BE, Ventura SJ, Osterman MJK, Mathews TJ. Births: final data for 2011. Natl Vital Stat Rep 2013; 62 (01) 1-69 , 72
  • 23 Martin JA, Hamilton BE, Osterman MJK, Curtin SC, Matthews TJ. Births: final data for 2012. Natl Vital Stat Rep 2013; 62 (09) 1-68
  • 24 Martin JA, Hamilton BE, Osterman MJ, Curtin SC, Matthews TJ. Births: final data for 2013. Natl Vital Stat Rep 2015; 64 (01) 1-65
  • 25 Hamilton BE, Martin JA, Osterman MJK, Curtin SC, Matthews TJ. Births: final data for 2014. Natl Vital Stat Rep 2015; 64 (12) 1-64
  • 26 Government of Canada SC. Live births, by month. Published September 28, 2021. Accessed March 2, 2022, at: https://www150.statcan.gc.ca/t1/tbl1/en/tv.action?pid=1310041501
  • 27 Dehdashtian M, Bashirnejad S, Malekian A, Aramesh MR, Aletayeb MH. Seasonality, epidemiology and outcome of congenital diaphragmatic hernia in south west of Iran. J Neonatal Surg 2017; 6 (02) 28
  • 28 Torfs CP, Curry CJ, Bateson TF, Honoré LH. A population-based study of congenital diaphragmatic hernia. Teratology 1992; 46 (06) 555-565
  • 29 Boyd R, McMullen H, Beqaj H, Kalfa D. Environmental exposures and congenital heart disease. Pediatrics 2022; 149 (01) e2021052151
  • 30 Black AJ, Lu DY, Yefet LS, Baird R. Sex differences in surgically correctable congenital anomalies: a systematic review. J Pediatr Surg 2020; 55 (05) 811-820
  • 31 Harting MT, Lally KP. The Congenital Diaphragmatic Hernia Study Group registry update. Semin Fetal Neonatal Med 2014; 19 (06) 370-375
  • 32 The Canadian Pediatric Surgery Network. CAPSNet 2019 Annual Report 2019. Published 2019. Accessed April 25, 2022, at: http://www.capsnetwork.org/portal/forResearchers/AnnualReportsandNewsletters.aspx
  • 33 Petrova VN, Russell CA. The evolution of seasonal influenza viruses. Nat Rev Microbiol 2018; 16 (01) 47-60
  • 34 Luteijn JM, Addor MC, Arriola L. et al. The association of H1N1 pandemic influenza with congenital anomaly prevalence in Europe: an ecological time series study. Epidemiology 2015; 26 (06) 853-861
  • 35 Fleck S, Bautista G, Keating SM. et al. Fetal production of growth factors and inflammatory mediators predicts pulmonary hypertension in congenital diaphragmatic hernia. Pediatr Res 2013; 74 (03) 290-298
  • 36 Wagner R, Lieckfeldt P, Piyadasa H. et al. Proteomic profiling of hypoplastic lungs suggests an underlying inflammatory response in the pathogenesis of abnormal lung development in congenital diaphragmatic hernia. bioRxiv. Published online January 1, 2022. DOI: 10.1101/2022.03.07.483298