Permanent Neonatal Diabetes in a Patient with a KCNJ11/Q52R Mutation Accompanied by Intermittent Hypoglycemia and Liver Failure
© N. D. Shaw and J. A. Majzoub. 2009
Received: 7 May 2009
Accepted: 16 July 2009
Published: 7 September 2009
The most common monogenic cause of neonatal diabetes is mutation in KCNJ11, which encodes a potassium channel in pancreatic beta cells. Some mutations in this gene, including Q52R, have been described in association with neurological deficits, but never with hepatic involvement. We report the second case of neonatal diabetes in a patient with a KCNJ11 Q52R mutation. This patient's clinical course did not include obvious neurological deficits despite the presence of prematurity, but did include transient hyperbilirubinemia, and recurrent hypoglycemia. The phenotypic spectrum of KCNJ11 mutations is variable and is likely influenced by additional genetic and environmental factors.
Neonatal diabetes mellitus (NDM) is a rare monogenic disorder that presents as hyperglycemia, failure to thrive, or diabetic ketoacidosis in the first 6 months of life . The permanent form of NDM is most commonly caused by a mutation in KCNJ11, the gene encoding the Kir6.2 subunit of the ATP-sensitive potassium channel. Kir6.2 assembles with SUR to form potassium channels in the beta cell, brain, heart, and muscle .
More than thirty mutations in KCNJ11 have been identified . Those mutations producing the most profound reduction in ATP sensitivity are associated with the most severe phenotype known as DEND syndrome (developmental delay, epilepsy, and NDM). A single patient with DEND harboring a Q52R mutation (c.155A>G) of KCNJ11 was reported in 2004  (referred to as ISPAD 27), and his clinical course has been described by Sumnik et al. . This patient was initially diagnosed with type 1 diabetes in the first week of life and treated with insulin. When his mutation was discovered at age 4, he was given a trial of glibenclamide but showed no response. He is currently 9 years old and has severe developmental delay and epilepsy.
Herein we describe a second case of a patient with a Q52R mutation in KCNJ11. In addition to NDM, his clinical course was notable for prematurity, severe hyperbilirubinemia and intermittent hypoglycemia unrelated to his diabetes treatment, features that have not been described in any other children with NDM. Notably, he did not have any obvious neurological deficits.
2. Case Report
Laboratory evaluation of patient SM to determine etiology of hypo- and hyperglycemia.
at blood glucose 12.3 mmol/L
at blood glucose 1.7 mmol/L
at blood glucose 12.3 mmol/L
H at 3 mo (%)
Pancreatic auto-antibodies (U/L)
after 62.5 mcg cortrosyn
Free thyroxine (pmol/L)
Laboratory evaluation of patient SM to determine etiology of liver failure.
Alpha-1-antitrypsin ( mol/L)
Total Protein (g/L)
Hepatitis Panel (B, C)
Newborn Screen for Cystic Fibrosis
At approximately 3 months of age (corrected age 37 weeks), the patient underwent a formal neurodevelopmental assessment. Despite his preceding critical illness, he demonstrated normal passive range of motion of all extremities, a strong grasp and suck, and was able to fixate on and scan faces and bring his hands to his mouth. The only deficit noted was a decrease in his spontaneous motor activity. By the time of discharge, at age 4 months of age (corrected age 2.5 weeks), however, he had achieved the same developmental milestones as had his healthy twin sister.
A diabetes nurse educator taught the patient's parents how to administer insulin and to use a glucometer on several occasions prior to discharge. He saw his pediatrician the day of discharge and appeared well but died unexpectedly in the middle of the night. There was no obvious cause of death and no autopsy was performed.
This report describes the unique phenotype of the second patient with NDM secondary to a Q52R mutation in KCNJ11. Unlike other patients with NDM, our patient had intermittent hypoglycemia (in addition to hyperglycemia), even when not being treated with insulin. Our patient was clearly at risk for hypoglycemia due to reduced hepatic glycogen stores associated with prematurity and liver disease. If these were the only contributing factors, however, one would expect his hypoglycemic episodes to have clustered early in the neonatal period, during periods of severe liver dysfunction, and with longer episodes of fasting. This is not the pattern depicted in Figure 1: his liver failure was progressive rather than episodic, he was prone to hypoglycemia before his bilirubin rose and after it returned to normal, and his hypoglycemia occurred both with fasting and after a meal.
Our patient was also unique in having idiopathic liver failure. Liver involvement has not been described in any patient with NDM, including ISPAD27. The majority of NDM patients, however, have not been vulnerable premature neonates subject to the same physiologic stressors as our patient, so the liver disease may have been solely related to factors associated with prematurity including hypoperfusion, infection, hypoxia, or drug effects. However, it is also possible that a KCNJ11 mutation increases one's susceptibility to liver failure but is only manifested in combination with other factors related to prematurity. As noted previously, Kir6.2 is widely expressed and has been detected in human liver cell lines , but its potential function in the liver has not been explored.
In summary, this patient represents the second reported case of NDM secondary to a Q52R mutation in KCNJ11 and the first report of NDM accompanied by hypoglycemia and liver failure. This patient's normal neurodevelopment, at least until 4 months (corrected age 2.5 weeks), was also unexpected given that the only other patient reported with NDM and this KCNJ11 mutation has DEND. Because the pathogenesis of developmental delay and epilepsy in DEND patients remains unknown, we believe that clinicians taking care of patients with NDM should carefully evaluate them for intermittent hypoglycemic insults as well as liver dysfunction.
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