Department of Internal Medicine, Chung Shan Medical University Hospital, Taichung, Taiwan.
School of Medicine, Chung Shan Medical University, Taichung, Taiwan.
Am J Perinatol. 2021 Oct;38(12):1244-1253. doi: 10.1055/s-0040-1708033. Epub 2020 Mar 13.
This study aimed to determine whether neonatal hyperbilirubinemia is associated with a risk of autism spectrum disorder (ASD) using a large population-based cohort.
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).
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).
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.
本研究旨在利用大型基于人群的队列,确定新生儿高胆红素血症是否与自闭症谱系障碍(ASD)的风险相关。
本回顾性队列研究使用了来自台湾国民健康保险研究数据库(1996-2012 年)儿童数据库(2000-2012 年)的数据。我们纳入了 2000 年至 2004 年期间出生且年龄<1 个月的患有和未患有高胆红素血症的新生儿。主要结局是医生诊断的 ASD。2012 年底,采用多变量 Cox 回归分析来估计风险比(HR)。
共有 67017 名新生儿被纳入研究。与未患有高胆红素血症的新生儿相比,患有高胆红素血症的新生儿患 ASD 的风险增加了 1.28 倍(HR=1.28,95%置信区间[CI]:1.05-1.57)。在确定高胆红素血症的光疗和换血治疗与 ASD 的关系的亚分析中,治疗与 ASD 之间无关联,表明高胆红素血症对 ASD 风险没有剂量反应效应。男孩患 ASD 的风险比女孩高近 6 倍(HR=5.89,95%CI:4.41-7.86)。此外,早产儿和低出生体重儿与 ASD 的风险相关(HR=1.46,95%CI:1.00-2.13)。
我们没有观察到高胆红素血症对 ASD 的剂量反应效应,但如果其他围产期并发症存在残余混杂,新生儿高胆红素血症可能是 ASD 的一个独立危险因素。因此,本研究不支持新生儿高胆红素血症暴露与 ASD 风险之间存在因果关系。