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Octreotide Diazoxide Somatostatin analogues
Genetics and mutation Paediatric endocrinology
Year of Publication
Signs and Symptoms
Failure to thrive
Asian ‐ Bangladeshi
Hyperinsulinaemia Congenital hyperinsulinism
Genetic analysis
Month of Publication
Country of Treatment
United Kingdom
Case Report Type
Unique/unexpected symptoms or presentations of a disease
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Paternally inherited ABCC8 mutation causing diffuse congenital hyperinsulinism

Suresh Chandran1, Fabian Yap Kok Peng2, Victor Samuel Rajadurai1, Yap Te Lu3, Kenneth T E Chang4, S E Flanagan5, S Ellard5 and Khalid Hussain6

[1] Departments of Neonatology, KK Women's and Children's Hospital, 100 Bukit Timah Road, Singapore 229899, Singapore

[2] Paediatric Endocrinology, KK Women's and Children's Hospital, 100 Bukit Timah Road, Singapore 229899, Singapore

[3] Paediatric Surgery, KK Women's and Children's Hospital, 100 Bukit Timah Road, Singapore 229899, Singapore

[4] Children's Pathology, KK Women's and Children's Hospital, 100 Bukit Timah Road, Singapore 229899, Singapore

[5] Institute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter EX2 5DW, UK

[6] Department of Paediatric Endocrinology, Great Ormond Street Hospital for Children NHS Trust, London WC1N 3JH, UK


background: Congenital hyperinsulinism (CHI) is a rare genetic disorder characterised by inappropriate insulin secretion in the face of severe hypoglycaemia. There are two histological subtypes of CHI namely diffuse and focal. Diffuse CHI is most common due to recessive mutations in ABCC8/KCNJ11 (which encode the SUR/KIR6.2 components of the pancreatic β-cell KATP channel) whereas focal CHI is due to a paternally inherited ABCC8/KCNJ11 mutation and somatic loss of heterozygosity for the 11p allele inside the focal lesion. Fluorine-18-l-dihydroxyphenylalanine positron emission tomography/computed tomography (18F-DOPA-PET/CT) is used in the pre-operative localisation of focal lesions prior to surgery. Diffuse CHI if medically unresponsive will require a near total pancreatectomy whereas focal CHI will only require a limited lesionectomy, thus curing the patient from the hypoglycaemia.

Aims: To report the first case of genetically confirmed CHI in Singapore from a heterozygous paternally inherited ABCC8 mutation.

Methods/Results: A term male infant presented with severe hyperinsulinaemic hypoglycaemia (HH) after birth and failed medical treatment with diazoxide and octreotide. Genetic testing (paternally inherited mutation in ABCC8/p.D1472N) suggested focal disease, but due to the unavailability of 18F-DOPA-PET/CT to confirm focal disease, a partial pancreatectomy was performed. Interestingly, histology of the resected pancreatic tissue showed changes typical of diffuse disease.

Conclusion: Heterozygous paternally inherited ABCC8/KCNJ11 mutations can lead to diffuse or focal CHI.

Learning points

  • HH is a cause of severe hypoglycaemia in the newborn period.

  • Paternal mutations in ABCC8/KCNJ11 can lead to diffuse or focal disease.

  • 18F-DOPA-PET/CT scan is the current imaging of choice for localising focal lesions.

  • Gallium-68 tetra-aza-cyclododecane-N NNN-‴-tetra-acetate octreotate PET scan is not a useful imaging tool for localising focal lesions.

  • The molecular mechanism by which a heterozygous ABCC8 mutation leads to diffuse disease is currently unclear.

  • Focal lesions are curable by lesionectomy and so genetic studies in patients with HH must be followed by imaging using 18F-DOPA-PET/CT scan.


Congenital hyperinsulinism (CHI) leads to severe hyperinsulinaemic hypoglycaemia (HH) in the neonatal, infancy and childhood periods. The genetic basis of CHI is beginning to be understood. Genetic studies are indicated in infants with persistent hypoglycaemia, hypoketonaemia and low fatty acid levels while requiring a glucose infusion rate (GIR) of more than 8 mg/kg per min to maintain euglycaemia (3.5–6.5 mmol/l). Most of the CHI cases are due to recessive or dominant mutations of ABCC8/KCNJ11 genes. The majority of the recessive mutations are resistant to medical treatment. Dominant forms are characterised by the various presentations and treatment responses. Initial management is aimed at correction of hypoglycaemia to prevent long-term neuro-disability. The response to diazoxide therapy is the key to managing CHI. Diazoxide unresponsiveness is considered as an indication for a rapid mutational analysis of ABCC8/KCNJ11 genes. Fluorine-18-l-dihydroxyphenylalanine positron emission tomography/computed tomography (18F-DOPA-PET/CT) scan is recommended if the genetic studies are suggestive of focal disease, which can then be cured by laparoscopic excision. We present the first case of proven CHI in Singapore in whom genetic studies suggested a focal lesion. 18F-DOPA-PET/CT scan is not available locally and the imaging using Gallium-68 tetra-aza-cyclododecane-N NNN-‴-tetra-acetate octreotate positron emission tomography (68G–DOTATATE-PET) and high-resolution ultrasound scan were non-conclusive. The infant underwent partial pancreatectomy with no improvement in the hypoglycaemia. Histopathology of the excised pancreas confirmed diffuse disease and the patient was subjected to near total pancreatectomy, with improvement of the HH. 18F-DOPA-PET/CT scanning facilities are only available in some centres around the world, thus making it difficult to identify all children with focal lesions.

Case presentation

A term male infant was born to non-consanguineous Asian parents by caesarean section. Maternal antenatal screen was unremarkable. His birth weight was 3230 g (50th–90th percentile) and length and head circumference were gestational age-appropriate. Apgar scores at birth were 9 at 1 min and 10 at 5 min. He was non-dysmorphic and systemic examination was unremarkable. At 3 h of life, he was noted to be lethargic and on checking his blood glucose level it was unrecordable. He was treated with i.v. glucose infusion and s.c. glucagon but remained hypoglycaemic even on a GIR of 12.6 mg/kg per min. During an episode of hypoglycaemia (1.2 mmol/l), his insulin level was 11.7 mU/l (Fig. 1). The serum growth hormone, lactate, ammonia and acylcarnitine levels were normal. His blood glucose levels normalised with a GIR of 16.4 mg/kg per min.

Figure 1

(A) Glucose and insulin profile during the treatment period. Medical and surgical treatments are plotted against the age of the patient. (B, i) Haematoxylin- and eosin-stained photomicrograph (magnification ×400). This shows a large islet with scattered enlarged and hyperchromatic nuclei (arrows). (B, ii) Haematoxylin- and eosin-stained photomicrograph (magnification ×400). This islet shows an endocrine cell with enlarged and hyperchromatic nucleus (arrow). (C) Pancreatic β-cell: with entry of glucose into the cell, an increase in ATP:ADP ratio occurs and this in turn close the KATP channel, resulting in depolarisation of the cell, allowing influx of calcium and finally exocytosis of vesicles leading to release of insulin.

(A) Glucose and insulin profile during the treatment period. Medical and surgical treatments are plotted against the age of the patient. (B, i) Haematoxylin- and eosin-stained photomicrograph (magnification ×400). This shows a large islet with scattered enlarged and hyperchromatic nuclei (arrows). (B, ii) Haematoxylin- and eosin-stained photomicrograph (magnification ×400). This islet shows an endocrine cell with enlarged and hyperchromatic nucleus (arrow). (C) Pancreatic β-cell: with entry of glucose into the cell, an increase in ATP:ADP ratio occurs and this in turn close the KATP channel, resulting in depolarisation of the cell, allowing influx of calcium and finally exocytosis of vesicles leading to release of insulin.

When feeds were commenced, hypoglycaemia recurred. The patient was started on diazoxide (with hydrochlorothiazide) at 10 mg/kg per day on day 3 and then increased to 20 mg/kg per day but continued to have persistent hypoglycaemia. As the patient failed to respond to diazoxide, s.c. octreotide was started at the dose of 10 μg/kg per day. His blood glucose profile remained labile and hence the dose of octreotide was increased to 20 μg/kg per day. As the patient was medically unresponsive to diazoxide, genetic studies were undertaken for the cause of HH.


Genetic studies were done in the molecular genetics laboratory in Exeter, UK. Sequence analysis for the ABCC8 gene showed a paternally inherited heterozygous missense mutation (p.D1472N; c.4414G>A) and failed to detect a change from the normal sequence in the KCNJ11 gene. A second ABCC8 mutation of maternal origin was not found by sequence or dosage analysis multiplex ligation-dependent probe amplification (MLPA). The sequence analysis included the coding regions, conserved splice sites and a recently reported deep intronic splicing mutation (1). This paternally inherited ABCC8 (p.D1472N) mutation was previously reported in a patient with a focal (tail) pancreatic lesion (2). As 18F-DOPA-PET/CT was unavailable locally in our country, 68G–DOTATATE-PET nuclear scan was done but the results were non-conclusive. A pre-operative high-resolution ultrasound scanning was attempted and a questionable small nodular focus, which distorted the anterior contour at the junction of the pancreatic body and medial tail region, was identified.


The patient failed to respond to diazoxide (up to 20 mg/kg per day) and his blood glucose levels could only be kept stable on a high dose of s.c. octreotide infusion. He therefore underwent partial pancreatectomy (50%) on day 103 of life, leaving the head and part of the body of pancreas. Post-operatively, he continued to have persistent HH (Fig. 1A) and the GIR remained high at 17 mg/kg per min to maintain normoglycaemia despite being on 20 μg/kg per day octreotide. Histopathological examination of the resected pancreas showed absence of any focal lesions. The pancreas had normally sized (Fig. 1Bi) to large (Fig. 1Bii) islets. The islets showed scattered endocrine cells with large and hyperchromatic nuclei (Fig. 1Bi and ii). These changes are consistent with typical diffuse disease. Owing to the persistent hypoglycaemia, he subsequently underwent a subtotal pancreatectomy (95%) on day 183 of life. In the immediate post-operative period, he required a GIR of 10 mg/kg per min to maintain normal blood glucose levels, but over the next 2 weeks, his blood glucose levels stabilised.

Outcome and follow-up

The patient required nasogastric tube feeding due to poor oro-pharyngeal coordination and he achieved full enteral feeds by the 30th post-operative day. Gastro-oesophageal reflux disease was treated with anti-reflux medication. He was discharged on day 244 of life with pre-feed home blood glucose monitoring and once-daily injections of octreotide (10 μg/kg per day), which was later discontinued on day 301 of life. His growth and neuro-developmental assessment at the age of 1 year was normal.


HH is the commonest cause of persistent and recurrent hypoglycaemia during the neonatal and infancy periods. Insulin inhibits gluconeogenesis and glycogenolysis and stimulates uptake of glucose in muscles and adipocytes, leading to hypoglycaemia. Moreover, insulin inhibits lipolysis and thereby ketone body synthesis. In effect, the brain of the baby with CHI is deprived of the primary (glucose) and secondary (ketones) energy sources due to inappropriately elevated insulin levels.

CHI is a genetically heterogeneous disease characterised by dysregulated insulin secretion from pancreatic β-cells (Fig. 1C). In the face of hypoglycaemia, infants with CHI have inappropriately elevated serum insulin, low ketone bodies, low fatty acids and show a glycaemic response to glucagon. Infants with CHI typically need a GIR of more than 8 mg/kg per min to maintain normoglycaemia (3). The incidence of sporadic forms of CHI is estimated at 1 in 40 000 live births, but in familial forms, it may be as high as 1 in 2500 with substantial consanguinity (3).

CHI has a strong genetic basis and mutations in the key genes (ABCC8, KCNJ11, GLUD1, GCK, HADH, SLC16A1, HNF4A, HNF1A and UCP2) regulating insulin secretion have been identified. Integrity of the pancreatic β-cell ATP-sensitive potassium (KATP) channel depends on the interactions between the pore-forming inward rectifier potassium channel subunit (KIR6.2) and the regulatory subunit sulfonylurea receptor 1 (SUR1). The ABCC8 and KCJN11 genes (both localised to chromosome 11p15.1) encode the two components of KATP channel and most of the severe forms of CHI are due to recessively inactivating mutations of these genes. CHI can be focal, diffuse or atypical but clinically indistinguishable (4).

CHI with a paternally inherited heterozygous mutation suggested focal disease as described by Hardy et al. (2). They reported a case of diazoxide-unresponsive CHI with the ABCC8/p.D1472N gene mutation and loss of heterozygosity (LOH), having focal CHI on 18F-DOPA-PET/CT study, which was cured by focal excision. As LOH is necessary in the pathogenesis of focal CHI, the LOH status by microsatellite study is important in infants with paternally inherited heterozygous ABCC8 mutations. In a study involving 36 Japanese infants with CHI, 84% had paternally inherited monoallelic mutations that accurately predicted the presence of the focal forms (5). Flanagan et al. (6) reported 150 homozygous, compound heterozygous and heterozygous inactivating mutations in ABCC8 gene and 24 mutations in the KCNJ11 gene. In a recent report of 300 patients with CHI, mutations were identified in only 45% of the patients, 36% being mutations in either ABCC8 or KCNJ11 gene. The focal forms seen in 40–50% of CHI cases occur due to the inheritance of paternal ABCC8/KCJN11 mutations and a somatic loss of the maternal chromosome 11p15 region with a paternal isodisomy at the same locus (7). A report on the molecular spectrum of 109 diazoxide-unresponsive patients with ABCC8 and KCNJ11 gene mutations concluded that in patients with single KATP channel mutations, 18F-DOPA-PET/CT imaging to differentiate focal and diffuse forms should follow genetic analysis (8).

In our particular case, the genetic analysis showed a paternally inherited ABCC8/p.D1472N mutation, predictive of focal disease. He underwent partial pancreatectomy on the basis of the genetic report and the suggestion of focal pancreatic lesion in the intra-operative high-resolution ultrasound scan. Imaging using 18F-DOPA-PET/CT is locally unavailable. Histopathology of the excised pancreas showed diffuse disease instead and the baby remained hypoglycaemic post-operatively. CHI due to large focal lesions can be excluded by histopathology and microsatellite analysis for LOH for maternal allele in the pancreatic lesion, the latter could not be done in our case. Autosomal dominant inheritance of CHI is unlikely given the previous case with a focal lesion (2) but cannot be ruled out. Dominant ABCC8 mutations typically cause diazoxide-responsive disease (3), but Flanagan et al. (9) reported dominant ABCC8 mutations in five patients from four families who were unresponsive to diazoxide and were cured by near total pancreatectomy. It is also possible that a second non-ABCC8/non-KCNJ11 mutation may be present causing the diffuse disease, as nearly 87% of diazoxide-unresponsive infants have either the ABCC8 or KCNJ11 mutation with the genetic cause of the remainder still unknown (7). The most likely explanation is that a maternally inherited ABCC8 mutation is present in a regulatory or intronic region of the gene but has not been detected by Sanger sequencing or dosage analysis. Next-generation sequencing provides a means to analyse the entire genomic region rather than just the coding exons and conserved splice sites (1) and is the logical next test.

A precise pre-operative assessment of CHI is now possible since the inception of 18F-DOPA-PET/CT scan, the current gold standard imaging technique having high specificity (100%) and sensitivity (88–94%) for focal lesions (2). The 68G–DOTATATE-PET nuclear scan used in our case is indicated primarily for the diagnosis of neuroendocrine tumours (10) and there is limited information on the role of high-resolution intraoperative ultrasound of the pancreas in CHI. This case demonstrates that 18F-DOPA-PET/CT imaging to confirm focal disease is essential in the management of infants with diazoxide-unresponsive CHI and a paternally inherited heterozygous mutation.

Diazoxide is the drug of choice for medical therapy once HH is confirmed (3). Diazoxide prevents β-cell membrane depolarisation and inhibits insulin secretion by keeping KATP channels open in patients who are diazoxide responsive, thereby allowing medical management without the need for pancreatectomy. Fluid retention and hypertrichosis are common with diazoxide use (3). Hypertrichosis was noted in the reported case while on diazoxide, which subsequently resolved on discontinuation. Most centres use chlorothiazide in conjunction with diazoxide to counteract the potential fluid retention side effects. Diazoxide is not useful in diffuse forms of CHI due to inactivating mutations in ABCC8 and KCNJ11 genes and in focal forms (3). If hypoglycaemia is unresponsive to diazoxide, a rapid genetic analysis for common mutations followed by imaging if indicated, facilitates differentiation of focal and diffuse forms in majority of patients with CHI. Laparoscopic focal excision is curative in focal forms whereas subtotal pancreatectomy leads to diabetes and exocrine pancreatic deficiency in most of the infants with diffuse disease (11).

The infants on treatment for CHI should have long-term developmental and visual follow-up because of the high risk of neurodevelopmental delay, cerebral palsy and epilepsy following hypoglycaemia-induced brain injury (12) (13).

Management of CHI is challenging even in developed countries due to lack of facilities for genetic studies and 18F-DOPA-PET/CT scan, currently limiting these diagnostic facilities only to specialised centres around the world. Diagnosis and treatment of our patient could have been expedited if these facilities were locally or regionally available.

Declaration of interest

The authors declare that there is no conflict of interest that could be perceived as prejudicing the impartiality of the research reported.


The genetic testing was funded by a Medical Research Council grant award to S Ellard and K Hussain. S Ellard is a Wellcome Trust Senior Investigator.

Patient consent

Written informed consent has been obtained from the father of the patient for publication of the submitted article and accompanying images.

Author contribution statement

S Chandran recruited the patient, collected data and wrote the manuscript. F Yap Kok Peng was directly involved in the management of the patient throughout the hospital stay and currently the lead person in the follow-up program. V S Rajadurai discussed and finalised all decisions related to the management of the patient. Y Te Lu is surgeon who performed the partial and subtotal pancreatectomy for this reported case. K T E Chang reported the pancreatic histopathology. S Flanagan carried out the genetic testing for KCNJ11 and ABCC8 gene mutations. S Ellard supervised the genetic testing and edited the final version of the manuscript. K Hussain helped to write the manuscript and edited the final version.



Flanagan SE, Xie W, Caswell R, Damhuis A, Vianey-Saban C, Akcay T, Darendeliler F, Bas F, Guven A, Siklar Z 2013 Next-generation sequencing reveals deep intronic cryptic ABCC8 and HADH splicing founder mutations causing hyperinsulinism by pseudoexon activation. American Journal of Human Genetics . 92: 131–136.(doi:10.1016/j.ajhg.2012.11.017)


Hardy OT, Pampaloni MH, Saffer JR, Suchi M, Ruchelli E, Zhuang H, Ganguly A, Freifelder R, Adzick NS, Alavi A 2007 Diagnosis and localization of focal congenital hyperinsulinism by 18F-flurodopa PET scan. Journal of Pediatrics . 150: 140–145.(doi:10.1016/j.jpeds.2006.08.028)


Senniappan S, Arya VB, & Hussain K 2013 The molecular mechanisms, diagnosis and management of congenital hyperinsulinism. Indian Journal of Endocrinology and Metabolism . 17: 19–30.(doi:10.4103/2230-8210.107822)


Mohammed Z, & Hussain K 2013 The genetics of hyperinsulinemic hypoglycemia. NeoReviews . 14: 179–188.(doi:10.1542/neo.14-4-e179)


Yorifuji T, Kawakita R, Nagai S, Sugimine A, Doi H, Nomura A, Masue M, Nishibori H, Yoshizawa A, Okamoto S 2011 Molecular and clinical analysis of Japanese patients with persistent congenital hyperinsulinism: predominance of paternally inherited monoallelic mutations in the KATP channel genes. Journal of Clinical Endocrinology and Metabolism . 96: E141–E145.(doi:10.1210/jc.2010-1281)


Flanagan SE, Clauin S, Bellanné-Chantelot C, de Lonlay P, Harries LW, Gloyn AL, & Ellard S 2009 Update of mutations in the genes encoding the pancreatic β-cell K (ATP) channel subunits Kir6.2 (KCNJ11) and sulfonylurea receptor 1 (ABCC8) in diabetes mellitus and hyperinsulinism. Human Mutation . 30: 170–180.(doi:10.1002/humu.20838)


Kapoor RR, Flanagan SE, Arya VB, Shield JP, Ellard S, & Hussain K 2013 Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism. European Journal of Endocrinology . 168: 557–564.(doi:10.1530/EJE-12-0673)


Bellanné-Chantelot C, Saint-Martin C, Ribeiro MJ, Vaury C, Verkarre V, Arnoux JB, Valayannopoulos V, Gobrecht S, Sempoux C, Rahier J 2010 ABCC8 and KCNJ11 molecular spectrum of 109 patients with diazoxide-unresponsive congenital hyperinsulinism. Journal of Medical Genetics . 11: 752–759.(doi:10.1136/jmg.2009.075416)


Flanagan SE, Kapoor RR, Banerjee I, Hall C, Smith VV, Hussain K, & Ellard S 2011 Dominantly acting ABCC8 mutations in patients with medically unresponsive hyperinsulinaemic hypoglycaemia. Clinical Genetics . 79: 582–587.(doi:10.1111/j.1399-0004.2010.01476.x)


Haug A, Auernhammer CJ, Wangler B, Tiling R, Schmidt G, Goke B, Bartestein P, & Popperl G 2009 Intraindividual comparison of 68Ga–DOTA-TATE and 18F-DOPA PET in patients with well-differentiated metastatic neuroendocrine tumours. European Journal of Nuclear Medicine and Molecular Imaging . 36: 765–770.(doi:10.1007/s00259-008-1030-8)


Bax KN, & van der Zee DC 2007 The laparoscopic approach towards hyperinsulinism in children. Seminars in Pediatric Surgery . 16: 245–251.(doi:10.1053/j.sempedsurg.2007.06.006)


Kumaran A, Kar S, Kapoor RR, & Hussain K 2010 The clinical problem of hyperinsulinemic hypoglycemia and resultant infantile spasms. Pediatrics . 126: 1231–1236.(doi:10.1542/peds.2009-2775)


Filan PM, Inder TE, Cameron FJ, Kean MJ, & Hunt RW 2006 Neonatal hypoglycemia and occipital cerebral injury. Journal of Pediatrics . 148: 552–555.(doi:10.1016/j.jpeds.2005.11.015)


(K Hussain is now at Developmental Endocrinology Research Group, Molecular Genetics Unit, Institute of Child Health, University College London, 30 Guildford Street, London WC1N 1EH, UK)