Literature DB >> 24057290

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

Katherine Lord1, Enyo Dzata, Kara E Snider, Paul R Gallagher, Diva D De León.   

Abstract

CONTEXT: Congenital hyperinsulinism (HI) occurs in two distinct histologic forms: diffuse and focal. Distinguishing between them is essential because a pancreatectomy is curative for focal HI and palliative for diffuse HI.
OBJECTIVE: The purpose of this study was to compare the presentations, treatment, and outcomes of diffuse and focal HI.
DESIGN: A retrospective chart review of children who underwent pancreatectomy for hyperinsulinism from December 2004 through September 2012 was conducted.
RESULTS: Based on pancreatic histology, 223 children were classified into 3 groups: diffuse (n = 97, 44%), focal (n = 114, 51%), and other (n = 12, 5%). Children with diffuse vs focal HI had significantly different mean gestational ages (38 vs 39 weeks, P < .0005) and birth weights (3963 vs 3717 g P = .012). Children with focal HI presented at an older age (0.3 vs 0 months, P < .0005) and more frequently with seizures (50 vs 25%, P < .0005). Children with diffuse HI had higher insulin levels during hypoglycemia (31.8 vs 12 μU/mL, P < .0005) and required higher glucose infusion rates (19.2 vs 16.1 mg/kg/min, P = .002). Children with diffuse HI had a median percent pancreactectomy of 98%, and postoperatively 41% required treatment for continued hypoglycemia. Children with focal HI had a median percent pancreatectomy rate of 27%, and 94% required no treatment after surgery.
CONCLUSIONS: Focal and diffuse HI present unique challenges, but the clinical differences between the 2 are subtle. Children with focal HI are at higher risk of delayed diagnosis and hypoglycemic seizures, but most are cured with surgery. In contrast, children with diffuse disease may be identified earlier, but face ongoing blood glucose abnormalities.

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Year:  2013        PMID: 24057290      PMCID: PMC3816257          DOI: 10.1210/jc.2013-2094

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


  9 in total

1.  Morphological mosaicism of the pancreatic islets: a novel anatomopathological form of persistent hyperinsulinemic hypoglycemia of infancy.

Authors:  C Sempoux; C Capito; C Bellanné-Chantelot; V Verkarre; P de Lonlay; Y Aigrain; C Fekete; Y Guiot; J Rahier
Journal:  J Clin Endocrinol Metab       Date:  2011-09-28       Impact factor: 5.958

2.  Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomy.

Authors:  P de Lonlay; J C Fournet; J Rahier; M S Gross-Morand; F Poggi-Travert; V Foussier; J P Bonnefont; M C Brusset; F Brunelle; J J Robert; C Nihoul-Fékété; J M Saudubray; C Junien
Journal:  J Clin Invest       Date:  1997-08-15       Impact factor: 14.808

3.  Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy.

Authors:  P Thomas; Y Ye; E Lightner
Journal:  Hum Mol Genet       Date:  1996-11       Impact factor: 6.150

4.  Genotype and phenotype correlations in 417 children with congenital hyperinsulinism.

Authors:  K E Snider; S Becker; L Boyajian; S-L Shyng; C MacMullen; N Hughes; K Ganapathy; T Bhatti; C A Stanley; A Ganguly
Journal:  J Clin Endocrinol Metab       Date:  2012-12-28       Impact factor: 5.958

Review 5.  Postnatal glucose homeostasis in late-preterm and term infants.

Authors:  David H Adamkin
Journal:  Pediatrics       Date:  2011-02-28       Impact factor: 7.124

6.  Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy.

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Journal:  Science       Date:  1995-04-21       Impact factor: 47.728

7.  Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia.

Authors:  V Verkarre; J C Fournet; P de Lonlay; M S Gross-Morand; M Devillers; J Rahier; F Brunelle; J J Robert; C Nihoul-Fékété; J M Saudubray; C Junien
Journal:  J Clin Invest       Date:  1998-10-01       Impact factor: 14.808

8.  Glucose metabolism in 105 children and adolescents after pancreatectomy for congenital hyperinsulinism.

Authors:  Jacques Beltrand; Marylène Caquard; Jean-Baptiste Arnoux; Kathleen Laborde; Gilberto Velho; Virginie Verkarre; Jacques Rahier; Francis Brunelle; Claire Nihoul-Fékété; Jean-Marie Saudubray; Jean-Jacques Robert; Pascale de Lonlay
Journal:  Diabetes Care       Date:  2011-12-21       Impact factor: 19.112

9.  Monogenic hyperinsulinemic hypoglycemia: current insights into the pathogenesis and management.

Authors:  Katherine Lord; Diva D De León
Journal:  Int J Pediatr Endocrinol       Date:  2013-02-06
  9 in total
  35 in total

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

Authors:  Changhong Li; Amanda M Ackermann; Kara E Boodhansingh; Tricia R Bhatti; Chengyang Liu; Jonathan Schug; Nicolai Doliba; Bing Han; Karen E Cosgrove; Indraneel Banerjee; Franz M Matschinsky; Itzhak Nissim; Klaus H Kaestner; Ali Naji; N Scott Adzick; Mark J Dunne; Charles A Stanley; Diva D De León
Journal:  Diabetes       Date:  2017-04-25       Impact factor: 9.461

2.  Late Presentation of Fulminant Necrotizing Enterocolitis in a Child with Hyperinsulinism on Octreotide Therapy.

Authors:  Colin Patrick Hawkes; N Scott Adzick; Andrew A Palladino; Diva D De León
Journal:  Horm Res Paediatr       Date:  2016-02-12       Impact factor: 2.852

Review 3.  Congenital hyperinsulinism disorders: Genetic and clinical characteristics.

Authors:  Elizabeth Rosenfeld; Arupa Ganguly; Diva D De Leon
Journal:  Am J Med Genet C Semin Med Genet       Date:  2019-08-14       Impact factor: 3.908

Review 4.  Genetic characteristics of patients with congenital hyperinsulinism.

Authors:  Mary Ellen Vajravelu; Diva D De León
Journal:  Curr Opin Pediatr       Date:  2018-08       Impact factor: 2.856

5.  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
Journal:  Clin Genet       Date:  2014-06-06       Impact factor: 4.438

6.  Congenital hyperinsulinism treated by surgical resection of the hyperplastic lesion which had been preoperatively diagnosed by 18F-DOPA PET examination in Japan: a nationwide survey.

Authors:  Yutaka Kanamori; Toshihiko Watanabe; Tohru Yorifuji; Michiya Masue; Hideyuki Sasaki; Masaki Nio
Journal:  Pediatr Surg Int       Date:  2018-08-03       Impact factor: 1.827

7.  High Risk of Diabetes and Neurobehavioral Deficits in Individuals With Surgically Treated Hyperinsulinism.

Authors:  Katherine Lord; Jerilynn Radcliffe; Paul R Gallagher; N Scott Adzick; Charles A Stanley; Diva D De León
Journal:  J Clin Endocrinol Metab       Date:  2015-09-01       Impact factor: 5.958

8.  A unique allosteric insulin receptor monoclonal antibody that prevents hypoglycemia in the SUR-1-/- mouse model of KATP hyperinsulinism.

Authors:  Puja Patel; Lawrenshey Charles; John Corbin; Ira D Goldfine; Kirk Johnson; Paul Rubin; Diva D De León
Journal:  MAbs       Date:  2018-06-01       Impact factor: 5.857

9.  Population pharmacokinetics of exendin-(9-39) and clinical dose selection in patients with congenital hyperinsulinism.

Authors:  Chee M Ng; Fei Tang; Steven H Seeholzer; Yixuan Zou; Diva D De León
Journal:  Br J Clin Pharmacol       Date:  2017-12-06       Impact factor: 4.335

10.  Novel perspectives of super-high dose sulfonylurea and high-dose oral prednisolone in an infant with DEND syndrome due to V64M heterozygote KCNJ11 mutation.

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Journal:  Acta Diabetol       Date:  2021-07-16       Impact factor: 4.280

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