Literature DB >> 26303612

Safety and Efficacy of Chronic Extended Release Cornstarch Therapy for Glycogen Storage Disease Type I.

Katalin M Ross1, Laurie M Brown1, Michelle M Corrado1, Tayoot Chengsupanimit1, Latravia M Curry1, Iris A Ferrecchia1, Laura Y Porras1, Justin T Mathew1, David A Weinstein2.   

Abstract

BACKGROUND: Glycogen storage disease type I (GSD I) causes severe hypoglycemia during periods of fasting since both glycogenolysis and gluconeogenesis are impaired. Primary treatment in North America consists of cornstarch therapy every 3-4 h. Waxy maize extended release cornstarch was introduced for maintaining overnight glucose concentrations, but no studies have assessed long-term safety and efficacy of the product.
OBJECTIVE: To demonstrate the safety and efficacy of modified cornstarch in GSD I.
DESIGN: An open-label overnight trial of extended release cornstarch was performed. Subjects with a successful trial (optimal metabolic control 2 or more hours longer than with traditional cornstarch) were given the option of continuing into the chronic observational phase. Subjects were assessed biochemically at baseline and after 12 months.
RESULTS: Of the 106 subjects (93 GSD Ia/13 GSD Ib), efficacy was demonstrated in 82 patients (88%) with GSD Ia and 10 patients (77%) with GSD Ib. The success rate for extending fasting was 95% for females and 78% for males. Of the patients who entered the longitudinal phase, long-term data are available for 44 subjects. Mean duration of fasting on traditional cornstarch prior to study for the cohort was 4.1 and 7.8 h on the extended release cornstarch (P < 0.001). All laboratory markers of metabolic control have remained stable in the chronically treated patients.
CONCLUSION: Extended release cornstarch appears to improve the quality of life of patients with GSD I without sacrificing metabolic control. Avoiding the overnight dose of cornstarch should enhance safety in this population.

Entities:  

Keywords:  Glycogen storage disease; Ketotic hypoglycemia; Uncooked cornstarch; Waxy maize extended release cornstarch

Year:  2015        PMID: 26303612      PMCID: PMC4864714          DOI: 10.1007/8904_2015_488

Source DB:  PubMed          Journal:  JIMD Rep        ISSN: 2192-8304


  15 in total

Review 1.  Glycogen storage diseases.

Authors:  Joseph I Wolfsdorf; David A Weinstein
Journal:  Rev Endocr Metab Disord       Date:  2003-03       Impact factor: 6.514

2.  Natural history of hepatocellular adenoma formation in glycogen storage disease type I.

Authors:  David Q Wang; Laurie M Fiske; Caroline T Carreras; David A Weinstein
Journal:  J Pediatr       Date:  2011-04-09       Impact factor: 4.406

3.  Glycogen storage disease: new approaches to therapy.

Authors:  J F Crigler; J Folkman
Journal:  Ciba Found Symp       Date:  1977

4.  Effect of continuous glucose therapy with uncooked cornstarch on the long-term clinical course of type 1a glycogen storage disease.

Authors:  David A Weinstein; Joseph I Wolfsdorf
Journal:  Eur J Pediatr       Date:  2002-07-31       Impact factor: 3.183

Review 5.  Glycogen storage disease types I and II: treatment updates.

Authors:  D D Koeberl; P S Kishnani; Y T Chen
Journal:  J Inherit Metab Dis       Date:  2007-02-16       Impact factor: 4.982

Review 6.  Hypoglycemia in childhood: long-term effects.

Authors:  Christina Flykanaka-Gantenbein
Journal:  Pediatr Endocrinol Rev       Date:  2004-08

7.  Psychosocial functioning in youth with glycogen storage disease type I.

Authors:  Eric Storch; Mary Keeley; Lisa Merlo; Marni Jacob; Catherine Correia; David Weinstein
Journal:  J Pediatr Psychol       Date:  2008-02-23

8.  A novel starch for the treatment of glycogen storage diseases.

Authors:  K Bhattacharya; R C Orton; X Qi; H Mundy; D W Morley; M P Champion; S Eaton; R F Tester; P J Lee
Journal:  J Inherit Metab Dis       Date:  2007-05-19       Impact factor: 4.982

9.  Regression of hepatocellular adenomas with strict dietary therapy in patients with glycogen storage disease type I.

Authors:  Richard D Beegle; Laurie M Brown; David A Weinstein
Journal:  JIMD Rep       Date:  2014-10-12

10.  A pilot longitudinal study of the use of waxy maize heat modified starch in the treatment of adults with glycogen storage disease type I: a randomized double-blind cross-over study.

Authors:  Kaustuv Bhattacharya; Helen Mundy; Maggie F Lilburn; Michael P Champion; David W Morley; François Maillot
Journal:  Orphanet J Rare Dis       Date:  2015-02-15       Impact factor: 4.123

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2.  Dietary Management of the Glycogen Storage Diseases: Evolution of Treatment and Ongoing Controversies.

Authors:  Katalin M Ross; Iris A Ferrecchia; Kathryn R Dahlberg; Monika Dambska; Patrick T Ryan; David A Weinstein
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3.  Development of minimally invasive 13C-glucose breath test to examine different exogenous carbohydrate sources in patients with glycogen storage disease type Ia.

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Review 4.  Glycogen metabolism in humans.

Authors:  María M Adeva-Andany; Manuel González-Lucán; Cristóbal Donapetry-García; Carlos Fernández-Fernández; Eva Ameneiros-Rodríguez
Journal:  BBA Clin       Date:  2016-02-27

5.  Glycogen storage disease type 1a is associated with disturbed vitamin A metabolism and elevated serum retinol levels.

Authors:  Ali Saeed; Joanne A Hoogerland; Hanna Wessel; Janette Heegsma; Terry G J Derks; Eveline van der Veer; Gilles Mithieux; Fabienne Rajas; Maaike H Oosterveer; Klaas Nico Faber
Journal:  Hum Mol Genet       Date:  2020-01-15       Impact factor: 6.150

6.  Use of waxy maize heat modified starch in the treatment of children between 2 and 5 years with glycogen storage disease type I: A retrospective study.

Authors:  Ghada Hijazi; Nisha Pai; Laura L Nagy; Sarah Herd; Jolynn Dickson; Maya Ram; Michal Inbar-Feigenberg
Journal:  Mol Genet Metab Rep       Date:  2019-11-06

Review 7.  Towards enhanced understanding of idiopathic ketotic hypoglycemia: a literature review and introduction of the patient organization, Ketotic Hypoglycemia International.

Authors:  Danielle Drachmann; Erica Hoffmann; Austin Carrigg; Beccie Davis-Yates; Valerie Weaver; Paul Thornton; David A Weinstein; Jacob S Petersen; Pratik Shah; Henrik Thybo Christesen
Journal:  Orphanet J Rare Dis       Date:  2021-04-13       Impact factor: 4.123

Review 8.  Glycogen Storage Disease Type Ia: Current Management Options, Burden and Unmet Needs.

Authors:  Terry G J Derks; David F Rodriguez-Buritica; Ayesha Ahmad; Foekje de Boer; María L Couce; Sarah C Grünert; Philippe Labrune; Nerea López Maldonado; Carolina Fischinger Moura de Souza; Rebecca Riba-Wolman; Alessandro Rossi; Heather Saavedra; Rupal Naik Gupta; Vassili Valayannopoulos; John Mitchell
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Review 9.  Glycogen storage diseases with liver involvement: a literature review of GSD type 0, IV, VI, IX and XI.

Authors:  Miriam Massese; Francesco Tagliaferri; Carlo Dionisi-Vici; Arianna Maiorana
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Review 10.  A patient with glycogen storage disease type 0 and a novel sequence variant in GYS2: a case report and literature review.

Authors:  Janez Jan Arko; Marusa Debeljak; Mojca Zerjav Tansek; Tadej Battelino; Urh Groselj
Journal:  J Int Med Res       Date:  2020-08       Impact factor: 1.671

  10 in total

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