Wolfsdorf Joseph I, Derks Terry G J, Drachmann Danielle, Shah Pratik, Thornton Paul S, Weinstein David A
Division of Endocrinology, Boston Children's Hospital, Department of Pediatrics, Harvard Medical School, Boston, Massachusetts, USA.
Section of Metabolic Diseases, Beatrix Children's Hospital, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Horm Res Paediatr. 2024 Mar 21:1-12. doi: 10.1159/000538483.
Sick children often have a decreased appetite and experience vomiting and diarrhea; however, hypoglycemia (plasma glucose concentration ≤50 mg/dL or 2.8 mmol/L) is rare. Ketotic hypoglycemia (KH) is the most common cause of hypoglycemia presenting to an Emergency Department in a previously healthy child between 6 months and 6 years of age. Ketosis and hypoglycemia are now well understood to be normal physiologic responses of young children to prolonged fasting.There is now substantial evidence that the term KH describes a variety of conditions including both the lower end of the normal distribution of fasting tolerance in young children as well as numerous rare disorders that impair fasting adaptation. Recent advances in molecular genetic testing have led to the discovery of these rare disorders. Idiopathic pathological KH is a diagnosis of exclusion that describes rare children who have abnormally limited fasting tolerance, experience recurrent episodes of KH, or develop symptoms of hypoglycemia despite elevated ketone levels, and in whom an explanation cannot be found despite extensive investigation. This review provides an approach to distinguishing between physiological KH and pathological KH and includes recommendations for management.
患病儿童通常食欲下降,并伴有呕吐和腹泻;然而,低血糖(血浆葡萄糖浓度≤50mg/dL或2.8mmol/L)较为罕见。酮症性低血糖(KH)是6个月至6岁以前健康儿童到急诊科就诊时低血糖最常见的原因。现在人们已经充分认识到,酮症和低血糖是幼儿对长期禁食的正常生理反应。现在有大量证据表明,“KH”一词描述了多种情况,包括幼儿空腹耐受正常分布的下限以及许多损害空腹适应能力的罕见疾病。分子基因检测的最新进展导致了这些罕见疾病的发现。特发性病理性KH是一种排除性诊断,描述的是那些空腹耐受异常受限、反复出现KH发作或尽管酮体水平升高仍出现低血糖症状且经过广泛检查仍无法找到病因的罕见儿童。本综述提供了区分生理性KH和病理性KH的方法,并包括管理建议。