Three cases of permanent neonatal diabetes mellitus: genotypes and management outcome.
- Author:
Hooi Leng OOI
1
;
Loo Ling WU
Author Information
1. Paediatric Endocrinology Unit, Department of Paediatrics, University Kebangsaan Malaysia Medical Centre, Jalan Yaacob Latif, Bandar Tun Razak, Cheras 56000, Kuala Lumpur, Malaysia. ooihooileng@hotmail.com
- Publication Type:Case Reports
- MeSH:
ATP-Binding Cassette Transporters;
genetics;
Blood Glucose;
metabolism;
Diabetes Mellitus;
genetics;
therapy;
Female;
Genotype;
Heterozygote;
Humans;
Infant;
Infant, Newborn;
Male;
Models, Biological;
Models, Genetic;
Molecular Biology;
Mutation;
Pancreas;
physiology;
Potassium Channels, Inwardly Rectifying;
genetics;
Quality of Life;
Receptors, Drug;
genetics;
Sulfonylurea Compounds;
therapeutic use;
Sulfonylurea Receptors
- From:Singapore medical journal
2012;53(7):e142-4
- CountrySingapore
- Language:English
-
Abstract:
Neonatal diabetes mellitus (DM) is defined as insulin-requiring DM in the first six months of life. Unlike type 1 DM, it is a monogenic disorder resulting from a de novo mutation in the genes involved in the development of the pancreas, β-cell mass or secretory function. The majority of neonatal DM cases are caused by a heterozygous activating mutation in the KCNJ11 or ABCC8 genes that encode the Kir6.2 and SUR1 protein subunits, respectively, in the KATP channel. Sulphonylurea, a KATP channel inhibitor, can restore insulin secretion, hence offering an attractive alternative to insulin therapy. We report three cases of neonatal DM and their genetic mutations. Two patients were successfully switched over to sulphonylurea monotherapy with resultant improvement in the quality of life and a more stable blood glucose profile. Patients with neonatal DM should undergo genetic evaluation. For patients with KCNJ11 and ABCC8 gene mutation, oral sulphonylurea should be considered.
