Clinical Research Unit, Khoo Teck Puat Hospital (KTPH), Singapore, Singapore.
Diabetes Centre, , Khoo Teck Puat Hospital (KTPH), Singapore, Singapore.
Eur J Hum Genet. 2019 Jun;27(6):989-993. doi: 10.1038/s41431-019-0371-z. Epub 2019 Mar 19.
A 22-year-old man was referred for continuation of diabetes mellitus treatment. He was first diagnosed with diabetes mellitus 2 months after birth, when he failed to thrive and showed symptoms of diabetic ketoacidosis. There was no family history of diabetes mellitus. The patient did not exhibit the full set of features to be qualified for any developmental delay, epilepsy and neonatal diabetes mellitus (DEND) syndrome. Insulin replacement therapy was initiated; however, management was challenged by wide glycemic excursion, hypoglycemic unawareness and insulin-associated cutaneous lipo-hypertrophy. Re-evaluation, including genetic testing, revealed a heterozygous missense p.Arg201Cys variation in the KCNJ11 gene encoding the potassium channel subunit Kir6.2. Successful treatment conversion from insulin to glibenclamide was achieved over an extended period of 2 months (up-titrating to a dose of 1.0 mg/kg) in this patient despite his long diabetes duration of 27 years with elimination of hypoglycemia unawareness and achievement of excellent glycemic control sustained over more than 5 years. This case highlights the importance of after having secured a firm genetic diagnosis, to undertake conversion to sulphonylurea with careful dose titration and perseverance over months. Confirmation of variants with functional implications by genetic testing in patients suspected of neonatal diabetes is important for accurate molecular diagnosis and precision-treatment strategy with optimal outcome.
一位 22 岁男性因需要继续治疗糖尿病而就诊。他出生后 2 个月被诊断患有糖尿病,当时他生长不良并出现糖尿病酮症酸中毒症状。家族中没有糖尿病病史。该患者没有表现出任何符合发育迟缓、癫痫和新生儿糖尿病(DEND)综合征的全部特征。虽然开始了胰岛素替代治疗,但由于血糖波动大、低血糖意识丧失和胰岛素相关皮肤脂肪肥厚,治疗管理仍具有挑战性。重新评估,包括基因检测,显示编码钾通道亚基 Kir6.2 的 KCNJ11 基因存在杂合错义 p.Arg201Cys 变异。尽管该患者患有长达 27 年的糖尿病,且存在低血糖意识丧失,血糖控制不佳,但通过延长 2 个月(逐渐增加至 1.0mg/kg 的剂量)的时间,成功将治疗从胰岛素转换为格列本脲,实现了血糖控制良好,且未出现低血糖。这个病例强调了在获得明确的基因诊断后,进行磺脲类药物转换的重要性,需要仔细调整剂量并坚持数月。对疑似新生儿糖尿病患者进行基因检测以确认具有功能意义的变异,对于进行准确的分子诊断和制定精准治疗策略以获得最佳结果非常重要。