Department of Paediatrics, 2nd Faculty of Medicine, Charles University in Prague and University Hospital Motol, Prague, Czech Republic.
Diabetes Care. 2013 Sep;36(9):2573-4. doi: 10.2337/dc13-0058. Epub 2013 Apr 22.
Hepatocyte nuclear factor-1A maturity-onset diabetes of the young (HNF1A-MODY) is a monogenic form of diabetes caused by heterozygous mutations in HNF1A. Currently, a history of diabetic ketoacidosis (DKA) is an exclusion criterion for genetic testing for MODY.
In this article, we describe two unrelated patients aged 17 and 24 years with severe DKA developed several years after the diagnosis of HNF1A-MODY.
Both patients were treated with insulin, but their metabolic control was poor (HbA1c 15%, 140 mmol/mol and 13%, 119 mmol/mol, respectively) due to noncompliance and missed insulin injections. In both patients, DKA followed a course of recurrent vomiting with dehydration and prerenal acute kidney injury. Their glycemia, blood pH, and base excess at admission were 97 mmol/L [1,748 mg/dL], 6.80, and -33 mmol/L (patient 1) and 34 mmol/L [613 mg/dL], 7.03, and -14 mmol/L (patient 2).
This anecdotal observation supports the notion that a history of DKA does not exclude MODY.
肝细胞核因子-1A 成年起病型糖尿病(HNF1A-MODY)是一种由 HNF1A 杂合突变引起的单基因糖尿病形式。目前,糖尿病酮症酸中毒(DKA)病史是 MODY 基因检测的排除标准。
本文描述了两名无关的 17 岁和 24 岁患者,他们在确诊 HNF1A-MODY 几年后出现严重的 DKA。
两名患者均接受胰岛素治疗,但由于不遵医嘱和漏注胰岛素,其代谢控制不佳(HbA1c 分别为 15%、140mmol/mol 和 13%、119mmol/mol)。在两名患者中,DKA 均继发于反复呕吐伴脱水和肾前性急性肾损伤。入院时,他们的血糖、血 pH 值和碱剩余分别为 97mmol/L[1,748mg/dL]、6.80 和-33mmol/L(患者 1)和 34mmol/L[613mg/dL]、7.03 和-14mmol/L(患者 2)。
这一偶然观察结果支持这样一种观点,即 DKA 病史并不能排除 MODY。