Literature DB >> 11241047

Protein-sensitive and fasting hypoglycemia in children with the hyperinsulinism/hyperammonemia syndrome.

B Y Hsu1, A Kelly, P S Thornton, C R Greenberg, L A Dilling, C A Stanley.   

Abstract

OBJECTIVE: Because the hyperinsulinism/hyperammonemia (HI/HA) syndrome is associated with gain of function mutations in the leucine-stimulated insulin secretion pathway, we examined whether protein feeding or fasting was responsible for hypoglycemia in affected patients. STUDY
DESIGN: Patients with HI/HA (8 children and 6 adults) were studied. All had dominantly expressed mutations of glutamate dehydrogenase and plasma concentrations of ammonium that were 2 to 5 times normal. The responses to a 24-hour fasting test were determined in 7 patients. Responses to a 1.5 gm/kg oral protein tolerance test in 12 patients were compared with responses of 5 control subjects.
RESULTS: The median age at onset of hypoglycemia in the 14 patients was 9 months; diagnosis was delayed beyond age 2 years in 6 patients, and 4 were not given a diagnosis until adulthood. Fasting tests revealed unequivocal evidence of hyperinsulinism in only 1 of 7 patients. Three did not develop hypoglycemia until 12 to 24 hours of fasting; however, all 7 demonstrated inappropriate glycemic responses to glucagon that were characteristic of hyperinsulinism. In response to oral protein, all 12 patients with HI/HA showed a fall in blood glucose compared with none of 5 control subjects. Insulin responses to protein loading were similar in the patients with HI/HA and control subjects.
CONCLUSION: The postprandial blood glucose response to a protein meal is more sensitive than prolonged fasting for detecting hypoglycemia in the HI/HA syndrome.

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Year:  2001        PMID: 11241047     DOI: 10.1067/mpd.2001.111818

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  46 in total

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Journal:  Arch Biochem Biophys       Date:  2011-11-04       Impact factor: 4.013

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Review 3.  Leucine metabolism in regulation of insulin secretion from pancreatic beta cells.

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4.  A case of hyperinsulinism/hyperammonaemia syndrome with reduced carbamoyl-phosphate synthetase-1 activity in liver: a pitfall in enzymatic diagnosis for hyperammonaemia.

Authors:  K Ihara; K Miyako; M Ishimura; R Kuromaru; H-Y Wang; K Yasuda; T Hara
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5.  A case of hyperinsulinism/hyperammonaemia syndrome: usefulness of the oral protein tolerance for the evaluation of treatment.

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Review 6.  Glutamate dehydrogenase: structure, allosteric regulation, and role in insulin homeostasis.

Authors:  Ming Li; Changhong Li; Aron Allen; Charles A Stanley; Thomas J Smith
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7.  Green tea polyphenols control dysregulated glutamate dehydrogenase in transgenic mice by hijacking the ADP activation site.

Authors:  Changhong Li; Ming Li; Pan Chen; Srinivas Narayan; Franz M Matschinsky; Michael J Bennett; Charles A Stanley; Thomas J Smith
Journal:  J Biol Chem       Date:  2011-08-03       Impact factor: 5.157

Review 8.  Approach to hypoglycemia in infants and children.

Authors:  Kajal Gandhi
Journal:  Transl Pediatr       Date:  2017-10

9.  Mechanism of hyperinsulinism in short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency involves activation of glutamate dehydrogenase.

Authors:  Changhong Li; Pan Chen; Andrew Palladino; Srinivas Narayan; Laurie K Russell; Samir Sayed; Guoxiang Xiong; Jie Chen; David Stokes; Yasmeen M Butt; Patricia M Jones; Heather W Collins; Noam A Cohen; Akiva S Cohen; Itzhak Nissim; Thomas J Smith; Arnold W Strauss; Franz M Matschinsky; Michael J Bennett; Charles A Stanley
Journal:  J Biol Chem       Date:  2010-07-29       Impact factor: 5.157

10.  Expression, purification and characterization of human glutamate dehydrogenase (GDH) allosteric regulatory mutations.

Authors:  Jie Fang; Betty Y L Hsu; Courtney M MacMullen; Mortimer Poncz; Thomas J Smith; Charles A Stanley
Journal:  Biochem J       Date:  2002-04-01       Impact factor: 3.857

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