Akiba Kazuhisa, Zukeran Hiroaki, Hasegawa Yukihiro, Fukami Maki
Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan.
Division of Endocrinology and Metabolism, Tokyo Metropolitan Children's Medical Center, Tokyo, Japan.
Clin Pediatr Endocrinol. 2024 Oct;33(4):224-228. doi: 10.1297/cpe.2024-0016. Epub 2024 Jul 20.
To date, heterozygous loss-of-function variants of have been identified in 13 families with diabetes. Here, we present initial clinical information regarding a young male with diabetes who carried a heterozygous nonsense variant of (p.Arg377Ter) previously reported in his family with diabetes. At 11 yr and 7 mo of age, the patient experienced severe thirst and hyperglycemia (331-398 mg/dL). Laboratory tests revealed elevated levels of glycated hemoglobin (HbA1c) (47 mmol/mL, 6.5%) and the Homeostatic Model for Insulin Resistance (HOMA-IR) (3.4). Blood glucose self-monitoring demonstrated grossly normal blood glucose levels, together with occasional postprandial hyperglycemia, and a few episodes of hypoglycemia. An oral glucose tolerance test revealed mild hyperglycemia and a delayed peak insulin level. His laboratory indices improved over two years with self-control of diet and exercise. These results indicate that the initial presentation of -variant-associated diabetes includes occasional hyperglycemia and hypoglycemia in response to changes in lifestyle. The possible association between variants and mild insulin resistance requires further validation in future studies.
迄今为止,在13个糖尿病家族中已鉴定出[基因名称]的杂合功能丧失变体。在此,我们提供了一名患有糖尿病的年轻男性的初步临床信息,他携带了其糖尿病家族中先前报道的[基因名称]杂合无义变体(p.Arg377Ter)。在11岁7个月大时,患者出现严重口渴和高血糖(331 - 398 mg/dL)。实验室检查显示糖化血红蛋白(HbA1c)水平升高(47 mmol/mL,6.5%)以及胰岛素抵抗稳态模型评估(HOMA-IR)升高(3.4)。血糖自我监测显示血糖水平总体正常,偶尔出现餐后高血糖,并有几次低血糖发作。口服葡萄糖耐量试验显示轻度高血糖和胰岛素水平峰值延迟。通过饮食和运动自我控制,他的实验室指标在两年内有所改善。这些结果表明,[基因名称]变体相关糖尿病的初始表现包括因生活方式改变而偶尔出现的高血糖和低血糖。[基因名称]变体与轻度胰岛素抵抗之间的可能关联需要在未来研究中进一步验证。