Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada,
Horm Res Paediatr. 2020;93(5):297-303. doi: 10.1159/000511139. Epub 2020 Nov 16.
Hyperinsulinism (HI), the most common neonatal cause of persistent hypoglycemia, can be associated with prolonged hospitalizations and risk for long-term neurological sequelae. Rapid identification of transient versus persistent forms of HI is crucial to optimize management.
The aims of the study were to assess the ability of clinical and biochemical features at presentation to predict transient versus persistent HI, and to evaluate differences in hospital outcomes.
This study is a retrospective review of 79 infants with HI admitted to the Hospital for Sick Children, Toronto, from 2012 to 2017. Patients were classified into 3 groups: transient and the 2 persistent forms, diazoxide responsive and diazoxide unresponsive (DU).
Infants with birth weight >90th percentile had an 8-fold increased risk of having a persistent form of HI (OR 8.8, 95% CI 2.5-30) and a 21-fold increased risk of having a DU form of HI (OR 21.1, 95% CI 4.9-91.8). The majority of children with transient HI and a birth weight >90th percentile were born to mothers with gestational diabetes. There were no other useful clinical or biochemical presenting features that differentiated the groups. There were significant differences in outcome measures, with the DU children more likely to require gastrostomy tube insertion and have an extended length of hospital admission.
A higher birth weight in the absence of maternal gestational diabetes is highly associated with a persistent form of HI. Given the marked difference in clinical outcomes between groups, expedited genetic testing should be considered in infants with this presentation to inform clinical management.
高胰岛素血症(HI)是新生儿持续性低血糖最常见的原因,可导致住院时间延长,并存在长期神经后遗症的风险。快速识别 HI 的短暂和持续形式对于优化管理至关重要。
本研究旨在评估发病时的临床和生化特征预测 HI 的短暂和持续形式的能力,并评估住院结局的差异。
这是一项对 2012 年至 2017 年期间在多伦多 SickKids 医院就诊的 79 例 HI 婴儿进行的回顾性研究。患者被分为 3 组:短暂性和 2 种持续性、地卓西平反应性和地卓西平无反应性(DU)。
出生体重>第 90 百分位数的婴儿持续性 HI 的风险增加 8 倍(OR 8.8,95%CI 2.5-30),DU 形式 HI 的风险增加 21 倍(OR 21.1,95%CI 4.9-91.8)。大多数体重>第 90 百分位数且出生时母亲患有妊娠期糖尿病的婴儿 HI 为短暂性。没有其他有用的临床或生化表现特征可以区分这些组。在结局测量方面存在显著差异,DU 患儿更有可能需要插入胃造口管,并延长住院时间。
在不存在母体妊娠期糖尿病的情况下,较高的出生体重与持续性 HI 高度相关。鉴于两组间临床结局存在明显差异,对于具有这种表现的婴儿应尽快进行基因检测,以便为临床管理提供信息。