Insulin autoimmune syndrome in a 3-year-old boy: the youngest to date in China and a narrow review.

IF 2 3区 医学 Q2 PEDIATRICS BMC Pediatrics Pub Date : 2025-02-04 DOI:10.1186/s12887-025-05395-0
Ming Cheng, Yuan Ding, Dongmei Wang, Chunxiu Gong
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Abstract

Background: Insulin autoimmune syndrome (IAS), characterized by endogenous hypoglycemia associated with insulin autoantibodies, is a rare cause of hypoglycemia in pediatric patients. Here, we report a case of the youngest patient with IAS in China, and summarize the clinical characteristics of the disease through a narrow review of pediatric cases.

Case presentation: A 3-year-10-month-old Chinese boy presented with unconsciousness. Initially, he was misdiagnosed with hyperinsulinemic hypoglycemia (HH) due to non-ketotic hypoglycemia. Whole exome sequencing (WES) was negative, and no pancreatic space-occupying lesions were identified. He continued to have intermittent episodes of symptomatic hypoglycemia. During an extended oral glucose tolerance test (OGTT), his insulin to C-peptide molar ratio was greater than 1, and anti-insulin antibodies (IAAs) measurements were as high as 54.38 COI (normal range 0-1 COI). High-resolution human leukocyte antigen (HLA) test showed a DRB1*08:03/*12:02 genotype. He was eventually diagnosed with IAS. Hypoglycemic episodes were not observed as long as the patient adhered to the low and frequent carbohydrate diet. Six months later, the patient's anti-insulin antibody had decreased to 10.17 COI, and mildly symptomatic hypoglycemia occasionally occurred in the case of noncompliance with the diet. Based on 11 studies from a literature review and our own case, a total of 12 pediatric patients were analyzed. Most of these patients presented with unconsciousness initially and their episodes of hypoglycemia do not follow a definitive pattern. Adjustments in diet serve as an effective intervention, and spontaneous remission is relatively common.

Conclusion: When differentiating the causes of HH in pediatric patients, IAS should not be overlooked. Elevated levels of IAAs and an inappropriate insulin to C-peptide molar ratio during an extended OGTT are critical indicators.

Clinical trial number: Not applicable.

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一名3岁男孩的胰岛素自身免疫性综合征:迄今为止中国最年轻的病例和一项狭隘的回顾
背景:胰岛素自身免疫综合征(IAS)以胰岛素自身抗体相关的内源性低血糖为特征,是儿科患者中一种罕见的低血糖病因。在此,我们报告一例中国最年轻的IAS患者,并通过对儿科病例的狭窄回顾总结该疾病的临床特征。病例介绍:一名3- 10个月大的中国男孩表现为意识不清。最初,由于非酮症性低血糖,他被误诊为高胰岛素性低血糖(HH)。全外显子组测序(WES)阴性,未发现胰腺占位性病变。他仍有间歇性的症状性低血糖发作。在延长的口服葡萄糖耐量试验(OGTT)中,他的胰岛素与c肽摩尔比大于1,抗胰岛素抗体(IAAs)测量值高达54.38 COI(正常范围0-1 COI)。高分辨率人白细胞抗原(HLA)检测显示为DRB1*08:03/*12:02基因型。他最终被诊断出患有IAS。只要患者坚持低碳水化合物饮食,就不会出现低血糖发作。6个月后,患者抗胰岛素抗体降至10.17 COI,饮食不遵医嘱时偶有轻度症状性低血糖。基于文献综述中的11项研究和我们自己的病例,我们共分析了12名儿科患者。大多数患者最初表现为无意识,其低血糖发作没有明确的模式。调整饮食是有效的干预措施,自发缓解是相对常见的。结论:鉴别小儿HH病因时,IAS不容忽视。在延长OGTT期间,IAAs水平升高和不适当的胰岛素与c肽摩尔比是关键指标。临床试验号:不适用。
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来源期刊
BMC Pediatrics
BMC Pediatrics PEDIATRICS-
CiteScore
3.70
自引率
4.20%
发文量
683
审稿时长
3-8 weeks
期刊介绍: BMC Pediatrics is an open access journal publishing peer-reviewed research articles in all aspects of health care in neonates, children and adolescents, as well as related molecular genetics, pathophysiology, and epidemiology.
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