Improved motor development and good long-term glycaemic control with sulfonylurea treatment in a patient with the syndrome of intermediate developmental delay, early-onset generalised epilepsy and neonatal diabetes associated with the V59M mutation in the KCNJ11 gene

被引:93
作者
Slingerland, A. S.
Nuboer, R.
Hadders-Algra, M.
Hattersley, A. T.
Bruining, G. J.
机构
[1] Erasmus Univ, Div Diabet, Med Ctr, Sophia Childrens Hosp, NL-3015 GJ Rotterdam, Netherlands
[2] Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter, Devon, England
[3] Leiden Univ, Med Ctr, Dept Cardiol, Leiden, Netherlands
[4] Meander Med Ctr, Dept Paediat, Amersfoort, Netherlands
[5] Univ Groningen, Med Ctr, Dept Neurol Dev Neurol, Groningen, Netherlands
基金
英国惠康基金;
关键词
developmental delay; glibenclamide; glyburide; KCNJ11; Kir6.2; neonatal diabetes; neurological features; sulfonylurea; sulphonylurea; V59M;
D O I
10.1007/s00125-006-0407-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims/hypothesis Activating mutations in the KCNJ11 gene encoding the Kir6.2 subunit of the K-ATP channels in pancreatic beta cells are a common cause of neonatal diabetes. One-third of patients also have developmental delay, which probably results from mutated K-ATP channels in muscle, nerve and brain. Sulfonylureas, which bind to the sulfonylurea receptor 1 subunit of the K-ATP channel, can replace insulin injections in patients with KCNJ11 mutations. The aim of this study was to investigate the long-term outcome and impact on neurological features of sulfonylurea treatment. Methods We report the response to sulfonylurea treatment in a boy with neonatal diabetes and marked developmental delay resulting from the KCNJ11 mutation V59M. Results Glibenclamide (glyburide) treatment was started at 23 months and resulted in insulin being discontinued, lower overall glycaemia, reduced glucose fluctuations and reduced hypoglycaemia. Good control (HbA(1c) 6.5%) was maintained 2 years after discontinuing insulin, despite a reduction in the glibenclamide dose (from 0.41 to 0.11 mg center dot kg(-1)center dot day(-1)). Within 1 month of starting glibenclamide there was marked improvement in motor function, resulting in the patient progressing from being unable to stand unaided to walking independently, but there was no improvement in mental function. Conclusions/interpretation This 2-year follow-up of a patient highlights that sulfonylurea treatment can result in prolonged, excellent glycaemic control and may improve motor features, but not mental features, associated with KCNJ11 mutations. This suggests that the neurological actions of sulfonylurea are initially principally on peripheral (nerve or muscle) rather than on central (brain) K-ATP channels. Early molecular diagnosis is important in patients with neonatal diabetes and neurological features.
引用
收藏
页码:2559 / 2563
页数:5
相关论文
共 24 条
[11]   Triggering and amplifying pathways of regulation of insulin secretion by glucose [J].
Henquin, JC .
DIABETES, 2000, 49 (11) :1751-1760
[12]   The identification of a R201H mutation in KCNJ11, which encodes Kir6.2, and successful transfer to sustained-release sulphonylurea therapy in a subject with neonatal diabetes:: evidence for heterogeneity of beta cell function among carriers of the R201H mutation [J].
Klupa, T ;
Edghill, E ;
Nazim, J ;
Sieradzki, J ;
Ellard, S ;
Hattersley, A ;
Malecki, M .
DIABETOLOGIA, 2005, 48 (05) :1029-1031
[13]   Glucose-receptive neurones in the rat ventromedial hypothalamus express KATP channels composed of Kir6.1 and SUR1 subunits [J].
Lee, K ;
Dixon, AK ;
Richardson, PJ ;
Pinnock, RD .
JOURNAL OF PHYSIOLOGY-LONDON, 1999, 515 (02) :439-452
[14]  
Matthews DR, 1998, DIABETIC MED, V15, P297, DOI 10.1002/(SICI)1096-9136(199804)15:4<297::AID-DIA572>3.3.CO
[15]  
2-N
[16]   Activation of ATP-sensitive K+ channels in the ventromedial hypothalamus amplifies counterregulatory hormone responses to hypoglycemia in normal and recurrently hypoglycemic rats [J].
McCrimmon, RJ ;
Evans, ML ;
Fan, XN ;
McNay, EC ;
Chan, O ;
Ding, YY ;
Zhu, WL ;
Gram, DX ;
Sherwin, RS .
DIABETES, 2005, 54 (11) :3169-3174
[17]   Molecular basis of Kir6.2 mutations associated with neonatal diabetes or neonatal diabetes plus neurological features [J].
Proks, P ;
Antcliff, JF ;
Lippiat, J ;
Gloyn, AL ;
Hattersley, AT ;
Ashcroft, FM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (50) :17539-17544
[18]   Hypoglycemia in children with type 1 diabetes mellitus - Risk factors, cognitive function, and management [J].
Ryan, CM ;
Becker, DJ .
ENDOCRINOLOGY AND METABOLISM CLINICS OF NORTH AMERICA, 1999, 28 (04) :883-+
[19]   Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2 -: Patient characteristics and initial response to sulfonylurea therapy [J].
Sagen, JV ;
Ræder, H ;
Hathout, E ;
Shehadeh, N ;
Gudmundsson, K ;
Bævre, H ;
Abuelo, D ;
Phornphutkul, C ;
Molnes, J ;
Bell, GI ;
Gloyn, AL ;
Hattersley, AT ;
Molven, A ;
Sovik, O ;
Njolstad, PR .
DIABETES, 2004, 53 (10) :2713-2718
[20]   Mutations in the Kir6.2 subunit of the KATP channel and permanent neonatal diabetes:: New insights and new treatment [J].
Slingerland, AS ;
Hattersley, AT .
ANNALS OF MEDICINE, 2005, 37 (03) :186-195