1型糖尿病和单基因糖尿病——两者能共存吗?]

Harefuah Pub Date : 2025-05-01
Nirit Aviran Barak
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引用次数: 0

摘要

这是一个35岁的男性病例,在16岁时因糖尿病酮症酸中毒(DKA)和谷氨酸脱羧酶(GAD)抗体阳性住院后被诊断为1型糖尿病(DM)。他的糖尿病从未得到很好的控制,并且有糖尿病和前驱糖尿病的家族史。他要求检查是否有单基因糖尿病,所以我们对这种情况进行了外显子组检查。令人惊讶的是,基因检测显示杂合子葡萄糖激酶(GCK)基因明显阳性,这是一种高致病性成熟型糖尿病(MODY) 2型。所有家庭成员均被纳入完整的外显子组小组,该小组尚未完成。在文献中,笔者发现了一些类似的病例报告。MODY2型糖尿病的遗传缺陷是葡萄糖磷酸化为葡萄糖6磷酸,葡萄糖6磷酸作为葡萄糖传感器;这会导致胰岛素分泌在较高的葡萄糖水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[TYPE 1 DIABETES MELLITUS AND MONOGENIC DIABETES - CAN THE TWO WALK TOGETHER?]

Introduction: This is a case of a 35-year-old man, diagnosed with type 1 diabetes mellitus (DM) at the age of 16 after hospitalization due to diabetic ketoacidosis (DKA) and positive glutamic acid decarboxylase (GAD) antibodies. His diabetes was never well controlled and there is a strong family history of diabetes and prediabetes as described. He asked to be checked for monogenic diabetes, so we conducted an exome panel for this condition. Surprisingly, the genetic testing was clearly positive for the heterozygote Glucokinase (GCK) gene, a highly pathogenic maturity-onset diabetes of the young (MODY) type 2. All family members were referred to complete exome panel, which is not yet complete. In the literature the author found a few similar case reports. The genetic defect in MODY2 diabetes is in the phosphorylation of glucose to glucose 6 phosphate which acts as a glucose sensor; this causes insulin secretion in higher glucose levels.

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