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
[1]   Chronic exposure to tolbutamide and glibenclamide impairs insulin secretion but not transcription of KATP channel components [J].
Ball, AJ ;
McCluskey, JT ;
Flatt, PR ;
McClenaghan, NH .
PHARMACOLOGICAL RESEARCH, 2004, 50 (01) :41-46
[2]   High-dose glibenclamide can replace insulin therapy despite transitory diarrhea in early-onset diabetes caused by a novel R201L Kir6.2 mutation [J].
Codner, E ;
Flanagan, S ;
Ellard, S ;
García, H ;
Hattersley, AT .
DIABETES CARE, 2005, 28 (03) :758-759
[3]   Transient neonatal diabetes mellitus is associated with a recurrent (R201H) KCNJ11 (KIR6.2) mutation [J].
Colombo, C ;
Delvecchio, M ;
Zecchino, C ;
Faienza, MF ;
Cavallo, L ;
Barbetti, F .
DIABETOLOGIA, 2005, 48 (11) :2439-2441
[4]   The epidemiology of the epilepsies in children [J].
Cowan, LD .
MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS, 2002, 8 (03) :171-181
[5]   Hypothalamic ATP-sensitive K+ channels play a key role in sensing hypoglycemia and triggering counterregulatory epinephrine and glucagon responses [J].
Evans, ML ;
McCrimmon, RJ ;
Flanagan, DE ;
Keshavarz, T ;
Fan, XN ;
McNay, EC ;
Jacob, RJ ;
Sherwin, RS .
DIABETES, 2004, 53 (10) :2542-2551
[6]  
Flykanaka-Gantenbein Christina, 2004, Pediatr Endocrinol Rev, V1 Suppl 3, P530
[7]   Relapsing diabetes can result from moderately activating mutations in KCNJ11 [J].
Gloyn, AL ;
Reimann, F ;
Proks, P ;
Pearson, ER ;
Temple, IK ;
Mackay, DJG ;
Shield, JPH ;
Freedenberg, D ;
Noyes, K ;
Ellard, S ;
Ashcroft, FM ;
Gribble, FM ;
Hattersley, AT .
HUMAN MOLECULAR GENETICS, 2005, 14 (07) :925-934
[8]   Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes [J].
Gloyn, AL ;
Pearson, ER ;
Antcliff, JF ;
Proks, P ;
Bruining, GJ ;
Slingerland, AS ;
Howard, N ;
Srinivasan, S ;
Silva, JMCL ;
Molnes, J ;
Edghill, EL ;
Frayling, TM ;
Temple, IK ;
Mackay, D ;
Shield, JPH ;
Sumnik, Z ;
van Rhijn, A ;
Wales, JKH ;
Clark, P ;
Gorman, S ;
Aisenberg, J ;
Ellard, S ;
Njolstad, PR ;
Ashcroft, FM ;
Hattersley, AT .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (18) :1838-1849
[9]   Sulphonylurea action revisited - the post-cloning era [J].
Gribble, FM ;
Reimann, F .
DIABETOLOGIA, 2003, 46 (07) :875-891
[10]   Activating mutations in Kir6.2 and neonatal diabetes - New clinical syndromes, new scientific insights, and new therapy [J].
Hattersley, AT ;
Ashcroft, FM .
DIABETES, 2005, 54 (09) :2503-2513