Literature DB >> 24827651

A 'picturesque' case of transition from subcutaneous to oral treatment in neonatal diabetes.

Stephanie Verstappen1, Dick Mul1.   

Abstract

We report a case of a 6-week-old infant with diabetes mellitus based on a genetic defect in the sulfonylurea receptor 1 (SUR1), an ATP-sensitive potassium (KATP) channel protein. A spectacular improvement in glucose regulation was shown by real-time continuous glucose monitoring when switching her from insulin to oral glibenclamide. Children with neonatal onset of diabetes deserve genetic testing in order to replace insulin with oral medication. 2014 BMJ Publishing Group Ltd.

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Year:  2014        PMID： 24827651      PMCID： PMC4025244          DOI： 10.1136/bcr-2013-202912

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN： 1757-790X


  6 in total

1.  Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir6.2 mutations.

Authors:  Ewan R Pearson; Isabelle Flechtner; Pål R Njølstad; Maciej T Malecki; Sarah E Flanagan; Brian Larkin; Frances M Ashcroft; Iwar Klimes; Ethel Codner; Violeta Iotova; Annabelle S Slingerland; Julian Shield; Jean-Jacques Robert; Jens J Holst; Penny M Clark; Sian Ellard; Oddmund Søvik; Michel Polak; Andrew T Hattersley
Journal:  N Engl J Med       Date:  2006-08-03       Impact factor: 91.245

2.  Sulfonylurea-responsive neonatal diabetes mellitus diagnosed through molecular genetics in two children and in one adult after a long period of insulin treatment.

Authors:  Lavinia Fanciullo; Brunella Iovane; Dimitra Gkliati; Giorgia Monti; Ivonne Sponzilli; Antonina Marta Cangelosi; Carla Matrorilli; Giovanni Chiari; Fabrizio Barbetti; Elisabetta Dall'Aglio; Maurizio Vanelli
Journal:  Acta Biomed       Date:  2012-04

3.  Aetiopathology and genetic basis of neonatal diabetes.

Authors:  J P Shield; R J Gardner; E J Wadsworth; M L Whiteford; R S James; D O Robinson; J D Baum; I K Temple
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  1997-01       Impact factor: 5.747

Review 4.  Management of diabetes mellitus in infants.

Authors:  Beate Karges; Thomas Meissner; Andrea Icks; Thomas Kapellen; Reinhard W Holl
Journal:  Nat Rev Endocrinol       Date:  2011-11-29       Impact factor: 43.330

5.  Mutations in ATP-sensitive K+ channel genes cause transient neonatal diabetes and permanent diabetes in childhood or adulthood.

Authors:  Sarah E Flanagan; Ann-Marie Patch; Deborah J G Mackay; Emma L Edghill; Anna L Gloyn; David Robinson; Julian P H Shield; Karen Temple; Sian Ellard; Andrew T Hattersley
Journal:  Diabetes       Date:  2007-04-19       Impact factor: 9.461

Review 6.  Diabetes mellitus and the β cell: the last ten years.

Authors:  Frances M Ashcroft; Patrik Rorsman
Journal:  Cell       Date:  2012-03-16       Impact factor: 41.582
  6 in total
  2 in total

1.  Hyperglycaemia induces metabolic dysfunction and glycogen accumulation in pancreatic β-cells.

Authors:  Melissa F Brereton; Maria Rohm; Kenju Shimomura; Christian Holland; Sharona Tornovsky-Babeay; Daniela Dadon; Michaela Iberl; Margarita V Chibalina; Sheena Lee; Benjamin Glaser; Yuval Dor; Patrik Rorsman; Anne Clark; Frances M Ashcroft
Journal:  Nat Commun       Date:  2016-11-24       Impact factor: 14.919

Review 2.  Neonatal Diabetes and the KATP Channel: From Mutation to Therapy.

Authors:  Frances M Ashcroft; Michael C Puljung; Natascia Vedovato
Journal:  Trends Endocrinol Metab       Date:  2017-03-03       Impact factor: 12.015
  2 in total

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