Literature DB >> 23275527

Genotype and phenotype correlations in 417 children with congenital hyperinsulinism.

K E Snider1, S Becker, L Boyajian, S-L Shyng, C MacMullen, N Hughes, K Ganapathy, T Bhatti, C A Stanley, A Ganguly.   

Abstract

CONTEXT: Hypoglycemia due to congenital hyperinsulinism (HI) is caused by mutations in 9 genes.
OBJECTIVE: Our objective was to correlate genotype with phenotype in 417 children with HI.
METHODS: Mutation analysis was carried out for the ATP-sensitive potassium (KATP) channel genes (ABCC8 and KCNJ11), GLUD1, and GCK with supplemental screening of rarer genes, HADH, UCP2, HNF4A, HNF1A, and SLC16A1.
RESULTS: Mutations were identified in 91% (272 of 298) of diazoxide-unresponsive probands (ABCC8, KCNJ11, and GCK), and in 47% (56 of 118) of diazoxide-responsive probands (ABCC8, KCNJ11, GLUD1, HADH, UCP2, HNF4A, and HNF1A). In diazoxide-unresponsive diffuse probands, 89% (109 of 122) carried KATP mutations; 2% (2 of 122) had GCK mutations. In mutation-positive diazoxide-responsive probands, 42% were GLUD1, 41% were dominant KATP mutations, and 16% were in rare genes (HADH, UCP2, HNF4A, and HNF1A). Of the 183 unique KATP mutations, 70% were novel at the time of identification. Focal HI accounted for 53% (149 of 282) of diazoxide-unresponsive probands; monoallelic recessive KATP mutations were detectable in 97% (145 of 149) of these cases (maternal transmission excluded in all cases tested). The presence of a monoallelic recessive KATP mutation predicted focal HI with 97% sensitivity and 90% specificity.
CONCLUSIONS: Genotype to phenotype correlations were most successful in children with GLUD1, GCK, and recessive KATP mutations. Correlations were complicated by the high frequency of novel missense KATP mutations that were uncharacterized, because such defects might be either recessive or dominant and, if dominant, be either responsive or unresponsive to diazoxide. Accurate and timely prediction of phenotype based on genotype is critical to limit exposure to persistent hypoglycemia in infants and children with congenital HI.

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Year:  2012        PMID: 23275527      PMCID: PMC3565119          DOI: 10.1210/jc.2012-2169

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  38 in total

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3.  Novel presentations of congenital hyperinsulinism due to mutations in the MODY genes: HNF1A and HNF4A.

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4.  HNF1A mutation presenting with fetal macrosomia and hypoglycemia in childhood prior to onset of overt diabetes.

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6.  Molecular and clinical analysis of Japanese patients with persistent congenital hyperinsulinism: predominance of paternally inherited monoallelic mutations in the KATP channel genes.

Authors:  Tohru Yorifuji; Rie Kawakita; Shizuyo Nagai; Akinori Sugimine; Hiraku Doi; Anryu Nomura; Michiya Masue; Hironori Nishibori; Akihiko Yoshizawa; Shinya Okamoto; Ryuichiro Doi; Shinji Uemoto; Hironori Nagasaka
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7.  ABCC8 mutation allele frequency in the Ashkenazi Jewish population and risk of focal hyperinsulinemic hypoglycemia.

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8.  Genome-wide homozygosity analysis reveals HADH mutations as a common cause of diazoxide-responsive hyperinsulinemic-hypoglycemia in consanguineous pedigrees.

Authors:  Sarah E Flanagan; Ann-Marie Patch; Jonathan M Locke; Teoman Akcay; Enver Simsek; Mohammadreza Alaei; Zeinab Yekta; Meena Desai; Ritika R Kapoor; Khalid Hussain; Sian Ellard
Journal:  J Clin Endocrinol Metab       Date:  2011-01-20       Impact factor: 6.134

9.  Diazoxide-unresponsive congenital hyperinsulinism in children with dominant mutations of the β-cell sulfonylurea receptor SUR1.

Authors:  Courtney M Macmullen; Qing Zhou; Kara E Snider; Paul H Tewson; Susan A Becker; Ali Rahim Aziz; Arupa Ganguly; Show-Ling Shyng; Charles A Stanley
Journal:  Diabetes       Date:  2011-05-02       Impact factor: 9.461

10.  Leucine-sensitive hyperinsulinaemic hypoglycaemia in patients with loss of function mutations in 3-Hydroxyacyl-CoA Dehydrogenase.

Authors:  Amanda J Heslegrave; Ritika R Kapoor; Simon Eaton; Bernadette Chadefaux; Teoman Akcay; Enver Simsek; Sarah E Flanagan; Sian Ellard; Khalid Hussain
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Review 2.  Perspective on the Genetics and Diagnosis of Congenital Hyperinsulinism Disorders.

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3.  Functional and Metabolomic Consequences of KATP Channel Inactivation in Human Islets.

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Journal:  Diabetes       Date:  2017-04-25       Impact factor: 9.461

4.  Structurally distinct ligands rescue biogenesis defects of the KATP channel complex via a converging mechanism.

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5.  Congenital hyperinsulinism: clinical and molecular characterisation of compound heterozygous ABCC8 mutation responsive to Diazoxide therapy.

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6.  Clinical presentation and management of children with diffuse and focal hyperinsulinism: a review of 223 cases.

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Review 7.  Genetic characteristics of patients with congenital hyperinsulinism.

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8.  Congenital Hypoglycemia Disorders: New Aspects of Etiology, Diagnosis, Treatment and Outcomes: Highlights of the Proceedings of the Congenital Hypoglycemia Disorders Symposium, Philadelphia April 2016.

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9.  Monoallelic ABCC8 mutations are a common cause of diazoxide-unresponsive diffuse form of congenital hyperinsulinism.

Authors:  C Saint-Martin; Q Zhou; G M Martin; C Vaury; G Leroy; J-B Arnoux; P de Lonlay; S-L Shyng; C Bellanné-Chantelot
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10.  Pharmacological Correction of Trafficking Defects in ATP-sensitive Potassium Channels Caused by Sulfonylurea Receptor 1 Mutations.

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Journal:  J Biol Chem       Date:  2016-08-29       Impact factor: 5.157

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