Bremer Andrew A, Ranadive Sayali, Lustig Robert H
Division of Endocrinology, Department of Pediatrics, University of California Davis Medical Center, Sacramento, CA 95817-2208, USA.
Pediatr Diabetes. 2008 Jun;9(3 Pt 1):236-9. doi: 10.1111/j.1399-5448.2007.00316.x. Epub 2008 Jan 24.
Neonatal diabetes mellitus is rare, may either be transient or permanent, and may be caused by mutations in any of the several different genes. Until recently, most forms of permanent neonatal diabetes required lifelong subcutaneous insulin for management; however, permanent neonatal diabetes due to activating mutations in the KCNJ11 gene, which encodes the Kir6.2 protein subunit of the ATP-sensitive K+ (K(ATP)) channel, may be amenable to oral sulfonylurea therapy. We describe a case of an 18-month-old infant with permanent neonatal diabetes due to an activating KCNJ11 mutation successfully transitioned from subcutaneous insulin therapy to oral sulfonylurea therapy in the outpatient setting.
新生儿糖尿病较为罕见,可分为暂时性或永久性,可能由几种不同基因中的任何一种发生突变引起。直到最近,大多数永久性新生儿糖尿病的治疗都需要终身皮下注射胰岛素;然而,由编码ATP敏感性钾离子(K(ATP))通道Kir6.2蛋白亚基的KCNJ11基因激活突变导致的永久性新生儿糖尿病,可能适合口服磺脲类药物治疗。我们描述了一例18个月大的永久性新生儿糖尿病婴儿病例,该婴儿因KCNJ11激活突变,在门诊环境中成功从皮下胰岛素治疗过渡到口服磺脲类药物治疗。