RSS-Feed abonnieren
DOI: 10.1055/s-0040-1708033
Is Neonatal Hyperbilirubinemia Exposure Associated with a Risk of Autism Spectrum Disorder? A Nationwide Cohort Study
Funding This study was supported by Chung Shan Medical University Hospital, Taichung, Taiwan (CSH-2013-C-011), the Taiwan Ministry of Health and Welfare Clinical Trial Centre (MOHW108-TDU-B-212–133004), China Medical University Hospital, Academia Sinica Stroke Biosignature Project (BM10701010021), and the Clinical Trial Consortium for Stroke (MOST 107–2321-B-039-004).Abstract
Objective This study aimed to determine whether neonatal hyperbilirubinemia is associated with a risk of autism spectrum disorder (ASD) using a large population-based cohort.
Study Design This retrospective cohort study used data from the children's database (2000–2012) of the National Health Insurance Research Database (1996–2012) in Taiwan. We included neonates who were born between 2000 and 2004 and aged <1 month diagnosed with and without hyperbilirubinemia. The primary outcome was physician-diagnosed ASD. At the end of 2012, multivariate Cox's regression analysis was used to estimate hazard ratios (HRs).
Results A total of 67,017 neonates were included. The neonates with hyperbilirubinemia were associated with 1.28-fold increased risk of ASD (HR = 1.28, 95% confidence interval [CI]: 1.05–1.57) compared with those without hyperbilirubinemia. In subanalysis to determine how phototherapy and exchange transfusion treatment for hyperbilirubinemia were associated with ASD showed no association between treatment and ASD, suggesting the lack of a dose-response effect of hyperbilirubinemia on the risk of ASD. Boys had a nearly six-fold higher risk of ASD than girls (HR = 5.89, 95% CI: 4.41–7.86). Additionally, neonates born with preterm birth and low birth weight were associated with a risk of ASD (HR = 1.46, 95% CI: 1.00–2.13).
Conclusion We did not observe a dose-response effect of hyperbilirubinemia on ASD, but neonatal hyperbilirubinemia may be an independent risk factor for ASD if there is a residual confounding by other perinatal complications. Therefore, this study does not support a causal link between neonatal hyperbilirubinemia exposure and the risk of ASD.
Keywords
autism spectrum disorder - neonatal hyperbilirubinemia - risk factor - boy - preterm birth and low birth weightEthical Approval
This study was approved by the hospital's Institutional Review Board (No.: CRREC-103–048) and informed consent was waived because of the retrospective nature of the study.
∗ These authors contributed equally to this work.
Publikationsverlauf
Eingereicht: 30. Juli 2019
Angenommen: 03. Februar 2020
Artikel online veröffentlicht:
13. März 2020
© 2020. Thieme. All rights reserved.
Thieme Medical Publishers
333 Seventh Avenue, New York, NY 10001, USA.
-
References
- 1 Lyall K, Croen L, Daniels J. et al. The changing epidemiology of autism spectrum disorders. Annu Rev Public Health 2017; 38 (01) 81-102
- 2 Baxter AJ, Brugha TS, Erskine HE, Scheurer RW, Vos T, Scott JG. The epidemiology and global burden of autism spectrum disorders. Psychol Med 2015; 45 (03) 601-613
- 3 Heeramun R, Magnusson C, Gumpert CH. et al. Autism and convictions for violent crimes: population-based cohort study in Sweden. J Am Acad Child Adolesc Psychiatry 2017; 56 (06) 491-497.e2
- 4 Hisle-Gorman E, Susi A, Stokes T, Gorman G, Erdie-Lalena C, Nylund CM. Prenatal, perinatal, and neonatal risk factors of autism spectrum disorder. Pediatr Res 2018; 84 (02) 190-198
- 5 Gardener H, Spiegelman D, Buka SL. Perinatal and neonatal risk factors for autism: a comprehensive meta-analysis. Pediatrics 2011; 128 (02) 344-355
- 6 Loke YJ, Hannan AJ, Craig JM. The role of epigenetic change in autism spectrum disorders. Front Neurol 2015; 6: 107
- 7 Mamidala MP, Polinedi A. P T v PK, et al. Prenatal, perinatal and neonatal risk factors of autism spectrum disorder: a comprehensive epidemiological assessment from India. Res Dev Disabil 2013; 34 (09) 3004-3013
- 8 Tordjman S, Somogyi E, Coulon N. et al. Gene × Environment interactions in autism spectrum disorders: role of epigenetic mechanisms. Front Psychiatry 2014; 5: 53
- 9 Finegan JA, Quarrington B. Pre-, peri-, and neonatal factors and infantile autism. J Child Psychol Psychiatry 1979; 20 (02) 119-128
- 10 Guinchat V, Thorsen P, Laurent C, Cans C, Bodeau N, Cohen D. Pre-, peri- and neonatal risk factors for autism. Acta Obstet Gynecol Scand 2012; 91 (03) 287-300
- 11 Kolevzon A, Gross R, Reichenberg A. Prenatal and perinatal risk factors for autism: a review and integration of findings. Arch Pediatr Adolesc Med 2007; 161 (04) 326-333
- 12 Hultman CM, Sparén P, Cnattingius S. Perinatal risk factors for infantile autism. Epidemiology 2002; 13 (04) 417-423
- 13 Bolton PF, Murphy M, Macdonald H, Whitlock B, Pickles A, Rutter M. Obstetric complications in autism: consequences or causes of the condition?. J Am Acad Child Adolesc Psychiatry 1997; 36 (02) 272-281
- 14 Ross G. Hyperbilirubinemia in the 2000s: what should we do next?. Am J Perinatol 2003; 20 (08) 415-424
- 15 Seidman DS, Paz I, Stevenson DK, Laor A, Danon YL, Gale R. Neonatal hyperbilirubinemia and physical and cognitive performance at 17 years of age. Pediatrics 1991; 88 (04) 828-833
- 16 Maimburg RD, Bech BH, Vaeth M, Møller-Madsen B, Olsen J. Neonatal jaundice, autism, and other disorders of psychological development. Pediatrics 2010; 126 (05) 872-878
- 17 Jangaard KA, Fell DB, Dodds L, Allen AC. Outcomes in a population of healthy term and near-term infants with serum bilirubin levels of >or=325 micromol/L (>or=19 mg/dL) who were born in Nova Scotia, Canada, between 1994 and 2000. Pediatrics 2008; 122 (01) 119-124
- 18 Maimburg RD, Vaeth M, Schendel DE, Bech BH, Olsen J, Thorsen P. Neonatal jaundice: a risk factor for infantile autism?. Paediatr Perinat Epidemiol 2008; 22 (06) 562-568
- 19 Lozada LE, Nylund CM, Gorman GH, Hisle-Gorman E, Erdie-Lalena CR, Kuehn D. Association of autism spectrum disorders with neonatal hyperbilirubinemia. Glob Pediatr Health 2015; 2: X15596518
- 20 Amin SB, Smith T, Wang H. Is neonatal jaundice associated with autism spectrum disorders: a systematic review. J Autism Dev Disord 2011; 41 (11) 1455-1463
- 21 Wu YW, Kuzniewicz MW, Croen L, Walsh EM, McCulloch CE, Newman TB. Risk of autism associated with hyperbilirubinemia and phototherapy. Pediatrics 2016; 138 (04) e20161813
- 22 Newman TB, Croen LA. Jaundice-autism link unconvincing. Pediatrics 2011; 127 (03) e858-e859
- 23 Croen LA, Yoshida CK, Odouli R, Newman TB. Neonatal hyperbilirubinemia and risk of autism spectrum disorders. Pediatrics 2005; 115 (02) e135-e138
- 24 Long J, Zhang S, Fang X, Luo Y, Liu J. Neonatal hyperbilirubinemia and Gly71Arg mutation of UGT1A1 gene: a Chinese case-control study followed by systematic review of existing evidence. Acta Paediatr 2011; 100 (07) 966-971
- 25 Huang MJ, Kua KE, Teng HC, Tang KS, Weng HW, Huang CS. Risk factors for severe hyperbilirubinemia in neonates. Pediatr Res 2004; 56 (05) 682-689
- 26 Johnson ES, Bartman BA, Briesacher BA. et al. The incident user design in comparative effectiveness research. Pharmacoepidemiol Drug Saf 2013; 22 (01) 1-6
- 27 Liu CY, Hung YT, Chuang YL. et al. Incorporating development stratification of Taiwan townships into sampling design of large scale health interview survey. J Health Manag 2006; 4 (01) 1-22
- 28 Loomes R, Hull L, Mandy WPL. What is the male-to-female ratio in autism spectrum disorder? a systematic review and meta-analysis. J Am Acad Child Adolesc Psychiatry 2017; 56 (06) 466-474
- 29 Pfaff DW, Rapin I, Goldman S. Male predominance in autism: neuroendocrine influences on arousal and social anxiety. Autism Res 2011; 4 (03) 163-176
- 30 Buchmayer S, Johansson S, Johansson A, Hultman CM, Sparén P, Cnattingius S. Can association between preterm birth and autism be explained by maternal or neonatal morbidity?. Pediatrics 2009; 124 (05) e817-e825
- 31 Olusanya BO, Emokpae AA, Zamora TG, Slusher TM. Addressing the burden of neonatal hyperbilirubinaemia in countries with significant glucose-6-phosphate dehydrogenase deficiency. Acta Paediatr 2014; 103 (11) 1102-1109
- 32 Yu MW, Hsiao KJ, Wuu KD, Chen CJ. Association between glucose-6-phosphate dehydrogenase deficiency and neonatal jaundice: interaction with multiple risk factors. Int J Epidemiol 1992; 21 (05) 947-952
- 33 Maimburg RD, Vaeth M. Perinatal risk factors and infantile autism. Acta Psychiatr Scand 2006; 114 (04) 257-264
- 34 Lampi KM, Lehtonen L, Tran PL. et al. Risk of autism spectrum disorders in low birth weight and small for gestational age infants. J Pediatr 2012; 161 (05) 830-836
- 35 Croen LA, Grether JK, Selvin S. Descriptive epidemiology of autism in a California population: who is at risk?. J Autism Dev Disord 2002; 32 (03) 217-224
- 36 Glasson EJ, Bower C, Petterson B, de Klerk N, Chaney G, Hallmayer JF. Perinatal factors and the development of autism: a population study. Arch Gen Psychiatry 2004; 61 (06) 618-627
- 37 Stein D, Weizman A, Ring A, Barak Y. Obstetric complications in individuals diagnosed with autism and in healthy controls. Compr Psychiatry 2006; 47 (01) 69-75
- 38 Bilder D, Pinborough-Zimmerman J, Miller J, McMahon W. Prenatal, perinatal, and neonatal factors associated with autism spectrum disorders. Pediatrics 2009; 123 (05) 1293-1300
- 39 Wilcox AJ. On the importance--and the unimportance--of birthweight. Int J Epidemiol 2001; 30 (06) 1233-1241
- 40 Breslau N. Psychiatric sequelae of low birth weight. Epidemiol Rev 1995; 17 (01) 96-106
- 41 Kim YS, Leventhal BL. Genetic epidemiology and insights into interactive genetic and environmental effects in autism spectrum disorders. Biol Psychiatry 2015; 77 (01) 66-74
- 42 Rutter M. Changing concepts and findings on autism. J Autism Dev Disord 2013; 43 (08) 1749-1757
- 43 Getahun D, Fassett MJ, Peltier MR. et al. Association of perinatal risk factors with autism spectrum disorder. Am J Perinatol 2017; 34 (03) 295-304