Diazoxide-Unresponsive Congenital Hyperinsulinism in Children With Dominant Mutations of the beta-Cell Sulfonylurea Receptor SUR1

作者：MacMullen Courtney M; Zhou Qing; Snider Kara E; Tewson Paul H; Becker Susan A; Aziz Ali Rahim; Ganguly Arupa; Shyng Show Ling; Stanley Charles A^*

来源：Diabetes, 2011, 60(6): 1797-1804.

DOI：10.2337/db10-1631

OBJECTIVE-Congenital hyperinsulinemic hypoglycemia is a group of genetic disorders of insulin secretion most commonly associated with inactivating mutations of the beta-cell ATP-sensitive K+ channel (K-ATP channel) genes ABCC8 (SUR1) and KCNJ11 (Kir6.2). Recessive mutations of these genes cause hyperinsulinism that is unresponsive to treatment with diazoxide, a channel agonist. Dominant K-ATP mutations have been associated with diazoxide-responsive disease. We hypothesized that some medically uncontrollable cases with only one K-ATP mutation might have dominant, diazoxide-unresponsive disease.
RESEARCH DESIGN AND METHODS-Mutations of the K-ATP genes were identified by sequencing genomic DNA. Effects of mutations on K-ATP channel function in vitro were studied by expression in COSm6 cells.
RESULTS-In 15 families with diazoxide-unresponsive diffuse hyperinsulism, we found 17 patients with a monoallelic missense mutation of SUR1. Nine probands had de novo mutations, two had an affected sibling or parent, and four had an asymptomatic carrier parent. Of the 13 different mutations, 12 were novel. Expression of mutations revealed normal trafficking of channels but severely impaired responses to diazoxide or MgADP. Responses were significantly lower compared with nine SUR1 mutations associated with dominant, diazoxide-responsive hyperinsulinism.
CONCLUSIONS-These results demonstrate that some dominant mutations of SUR1 can cause diazoxide-unresponsive hyperinsulinism. In vitro expression studies may be helpful in distinguishing such mutations from dominant mutations of SUR1 associated with diazoxide-responsive disease. Diabetes 60:17971804, 2011

• 出版日期2011-6