If you or your child have been diagnosed with Congenital Hyperinsulinism, the information below should be your first stop for finding out more about this disease.

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Congenital Hyperinsulinism

Frequently Used Abbreviations: CH: Congenital Hyperinsulinism; GK: glucokinase; GDH: glutamate dehydrogenase; HI: Hyperinsulinism; KATP channel: ATP-regulated potassium channel; SCHAD: short-chain 3-hydroxyacyl-CoA dehydrogenase

Introduction

Congenital Hyperinsulinism (CH), which is also known as familial hyperinsulinism (FHI) or persistent hyperinsulinemic hypoglycemia of infancy (PHHI), is the most frequent cause of severe, persistent hypoglycemia in newborns and children. In 25-40% of affected neonates, CH leads to lasting consequences such as developmental delay, mental retardation, or even death (1). CH is due to unregulated insulin release from either the entire pancreas (diffuse CH) or confined pancreatic areas (focal CH). In most countries, CH occurs at an approximate frequency of 1/25,000 to 1/50,000 live births.

To date, mutations in any one of five different genes have been associated with CH. Depending on the underlying genetic defect, prognosis and treatment of CH may vary. While CH due to mutations in GLUD1, GCK, or HADHSC are generally responsive to drug therapy, CH associated with mutations in ABCC8 or KCNJ11 often requires variable degrees of pancreatectomy (2, 3). Mutations in ABCC8 or KCNJ11 can cause both focal CH, which can be cured by partial pancreatectomy, and diffuse CH, which may require near-total pancreatectomy, potentially leading to life-long sequelae (4).

Genetic testing for CH-associated mutations in ABCC8, KCNJ11, GLUD1, and GCK can diagnose about 85% (5) of the most severe cases of CH. In addition, genetic testing may allow distinction between diffuse and focal forms of ABCC8- or KCNJ11-associated CH in many cases and identify cases of CH that are likely to respond to drug therapy (6).

KATP Hyperinsulinism (KATP HI)

KATP HI is due to loss-of-function mutations in either ABCC8 or KCNJ11, which encode the two protein components (Sur1 and Kir6.2, respectively) of the ATP-regulated potassium channels (KATP channels) in the membrane of pancreatic ß-cells (2). Closing of the KATP channels represents a crucial step in the complex chain of events that links a rise in blood glucose concentration to insulin release (see Normal Physiology of Insulin Release). In KATP HI, KATP channels are defective and remain closed most of the time, decoupling insulin release from the blood glucose concentration.

Of note, gain-of-function mutation in KCNJ11 do not lead to CH, but to the “complementary” condition, neonatal diabetes mellitus (7)

 

If you want to learn more about Normal Physiology of Insulin Release please click here.

Glutamate Dehydrogenase Hyperinsulinism (GDH HI)

GDH HI is due to gain-of-function mutations in GLUD1, the gene for the enzyme glutamate dehydrogenase (GDH) (8). GDH catalyzes the oxidative deamination of glutamate, leading to a rise in the intracellular ATP/ADP ratio. GDH activity is stimulated by leucine and inhibited by GTP. CH-associated mutations in GDH lower the enzyme’s sensitivity to its inhibitor GTP, allowing increased enzymatic activity in response to leucine. In pancreatic ß-cells, the increased GDH activity can give rise to an intracellular ATP/ADP ratio sufficient to trigger insulin release, decoupling insulin release from blood glucose concentration.

Glucokinase Hyperinsulinism (GK HI)

GK HI is due to gain-of-function mutations in GCK, the gene for the enzyme glucokinase (GK) (9). GK catalyzes the first and rate-limiting step of glycolysis and thus determines the rate of ATP production in ß-cells in response to the blood glucose concentration. If GK activity is increased due to a gain-of-function mutation, an intracellular ATP/ADP ratio sufficient to trigger insulin release is reached at lower than normal glucose concentrations.

Of note, loss-of-function mutations in GCK do not lead to CH, but to the "complementary" condition, diabetes mellitus (10, 11).

SCHAD Hyperinsulinism (SCHAD HI)

SCHAD HI is due to loss-of-function mutations in HADHSC, the gene for the enzyme short-chain 3-hydroxyacyl-CoA dehydrogenase (SCHAD) (3, 12). SCHAD is involved in fatty acid oxidation.

Congenital Hyperinsulinism Due to Unknown Causes

In about 45% of all cases, the cause of CH is not clear. It is likely that at least some of these cases are due to regulatory or intronic mutations or major deletions/ rearrangements in the five genes known to be associated with CH (13). In addition, mutations in other, as yet unidentified, genes may lead to CH.

Clinical Presentation of CH

KATP HI can occur in a diffuse and a focal form. Focal CH has been estimated to account for 40-70% of all cases of CH requiring pancreatectomy, with the remainder due to diffuse CH (6, 14, 15). Patients with KATP HI usually have high birth weights and present with severe hypoglycemia during the first days of life. In addition, they often manifest hypotonia, poor feeding, and apnea. Exceptions to this rule are cases of diffuse KATP HI caused by rare dominant mutations in ABCC8; such autosomal dominant diffuse KATP HI is associated with a much milder phenotype (16, 17, 18).

GDH HI is a diffuse form of CH and typically much milder than KATP HI, so that it may not be recognized until the affected infant is several months old (19). GDH HI is characterized by post-prandial hypoglycemic episodes and mildly elevated, apparently asymptomatic plasma ammonia levels. GDH HI is also known as hyperinsulinism-hyperammonemia syndrome.

GK HI is a diffuse form of CH with a typically very mild phenotype, although a severe case of GK HI has also been reported (20). Onset of presentation can range from infancy to adulthood (9, 21, 22).

SCHAD HI is a diffuse form of CH that presents during infancy. The phenotype can range from mild to severe (3, 12).

Diagnosis of CH

CH is suspected in infants and young children with episodes of spontaneous severe hypoglycemia lasting longer than 48 hours. Since insulin levels in patients with CH may fluctuate widely over time, diagnosis cannot always be achieved by demonstrating an elevated blood insulin concentration at the time of hypoglycemia. Other signs of unregulated insulin action are hypoglycemia during glucose infusion, low blood levels of free fatty acids and ketones at the time of hypoglycemia, and a rise in blood glucose after glucagon administration at the time of hypoglycemia. A fasting study may be required to provoke hypoglycemia and confirm the diagnosis of CH. Due to the genetics of CH, a family history of CH is not always apparent.

It is important to distinguish between KATP HI, GDH HI, and GK HI, because treatment options may vary drastically. In addition, focal and diffuse KATP HI should be differentiated, since focal KATP HI can potentially be cured by partial pancreatectomy.

KATP HI can often, but not always, be identified through acute insulin response studies (for details, see call-out) (23). GDH HI is characterized by elevated plasma ammonia levels and leucine-sensitive hypoclycemia; however, leucine-sensitivity has also been described in the case of KATP HI (18). Presence of 3-hydroxyglutaric acid in urine and raised plasma levels of 3-hydroxybutyryl-carnitine are indicative of SCHAD HI (3).

Differentiation between the diffuse and the focal form of KATP HI is difficult. Acute insulin response studies cannot reliably distinguish between these two forms of KATP HI (15, 24), and even highly involved procedures such as pancreatic arterial stimulation venous sampling or transhepatic portal venous sampling are only 70-80% accurate in differentiating diffuse and focal CH (15). Preliminary reports indicate that 18F-DOPA PET scans may be useful for localizing focal lesions (25).

Genetic testing allows differential diagnosis of GK HI, GDH HI, and KATP HI without lengthy, complicated, and potentially ambiguous diagnostic studies. In addition, genetic testing can help to distinguish between the diffuse and the focal form of KATP HI. Arterial stimulation venous sampling or transhepatic portal venous sampling can then be used to localize the focal lesion within the pancreas.

 

If you want to learn more about:

• Acute Insulin Response Studies please click here.
• Arterial Stimulation Venous Sampling (ASVS) please click here.
• Transhepatic Portal Venous Sampling (THPVS) please click here.

Treatment of CH

GK HI, GDH HI, SCHAD HI, and autosomal dominant diffuse KATP HI due to rare, specific autosomal dominant mutations in ABCC8 (16, 17, 18) are usually responsive to diazoxide, which is believed to inhibit insulin secretion through opening KATP channels. In contrast, most cases of diffuse and focal KATP HI cannot be adequately managed with diazoxide, since KATP channels are non-functional. Instead, octreotide (a somatostatin analogue) or continuous dextrose is used for therapy. However, in most cases of KATP HI, drug therapy fails, and pancreatectomy is required (4).

In patients suffering from diffuse KATP HI, typically over 95% of the pancreas has to be removed to avoid recurrent hypoglycemia. This near-total pancreatectomy can lead to life-long diabetes. In focal KATP HI, by contrast, only the part of the pancreas containing ß-cells with defective KATP channels has to be removed. Such partial pancreatectomy can offer a cure for focal KATP HI.

Genetics of CH

Diffuse KATP HI is generally inherited in an autosomal recessive manner. In rare cases, specific autosomal dominant mutations in ABCC8 can lead to a mild form of diffuse KATP HI.

Focal KATP HI is inherited in an autosomal dominant manner, due to somatic loss of heterozygosity (14). In this form of KATP HI, only the paternally inherited allele of ABCC8 or KCNJ11 contains a disease-linked mutation, while the maternal copy is normal. The CH phenotype is only expressed in those ß-cells and their clonal descendants where a somatic event has led to loss of the maternal allele; these cells create the focal lesion in the pancreas. The obligate paternal inheritance of the mutation leading to focal KATP HI may be associated with genomic imprinting.

GDH HI and GK HI are both inherited in an autosomal dominant manner. Most GHD HI cases identified to date are due to sporadic de novo mutations (19).

SCHAD HI is inherited in an autosomal recessive manner.

 

The above information is reproduced with permission from Athena Diagnostics.

http://www.athenadiagnostics.com/content/diagnostic-ed/endocrinology/hyperinsulinism