Volume 43, Issue 2 pp. 269-278
ORIGINAL ARTICLE

Cornstarch requirements of the adult glycogen storage disease Ia population: A retrospective review

Kathryn R. Dahlberg

Kathryn R. Dahlberg

Glycogen Storage Disease Program, Connecticut Children′s Medical Center, Hartford, Connecticut

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Iris A. Ferrecchia

Iris A. Ferrecchia

Glycogen Storage Disease Program, Connecticut Children′s Medical Center, Hartford, Connecticut

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Monika Dambska-Williams

Monika Dambska-Williams

Glycogen Storage Disease Program, Connecticut Children′s Medical Center, Hartford, Connecticut

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Traci E. Resler

Traci E. Resler

Glycogen Storage Disease Program, Connecticut Children′s Medical Center, Hartford, Connecticut

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Katalin M. Ross

Katalin M. Ross

Glycogen Storage Disease Program, Connecticut Children′s Medical Center, Hartford, Connecticut

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Gail L. Butler

Gail L. Butler

Glycogen Storage Disease Program, Connecticut Children′s Medical Center, Hartford, Connecticut

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Chia-Ling Kuo

Chia-Ling Kuo

Department of Community Medicine and Health Care, University of Connecticut School of Medicine, Farmington, Connecticut

Connecticut Institute for Clinical and Translational Science, Farmington, Connecticut

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Patrick T. Ryan

Patrick T. Ryan

Glycogen Storage Disease Program, Connecticut Children′s Medical Center, Hartford, Connecticut

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David A. Weinstein

Corresponding Author

David A. Weinstein

Glycogen Storage Disease Program, Connecticut Children′s Medical Center, Hartford, Connecticut

Department of Pediatrics, University of Connecticut School of Medicine, Farmington, Connecticut

Correspondence

David A. Weinstein, Glycogen Storage Disease Program, University of Connecticut and Connecticut Children′s Medical Center, 282 Washington Avenue, Hartford, CT 06106.

Email: [email protected]

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First published: 15 August 2019
Citations: 16
Funding information Global Center for Glycogen Storage Disease, Grant/Award Number: NA

Abstract

Cornstarch has been the primary treatment for glycogen storage disease type Ia (GSD Ia) for over 35 years. When cornstarch was first described as a treatment, few people survived beyond early childhood. As the prognosis for this population has improved, the need to ensure appropriate cornstarch dosing for different age groups has become imperative. Records from 115 patients (10-62 years of age) with GSD Ia evaluated at our center between 2015 and 2017 were reviewed. Data collected included weight, age, genetic mutation, amount and frequency of cornstarch doses, body mass index, gender, 24-hour glucose and lactate concentrations, and biochemical markers of metabolic control. The data demonstrate that adult treatment needs vary greatly from younger age groups, and the required cornstarch support decreases with age (P < .001). The required number of doses, however, did not change with a mean of six doses (range 4-8) daily in all age groups. General laboratory findings across time demonstrate that significantly reducing the amount of starch required to maintain euglycemia with aging can be done without sacrificing metabolic control. Carbohydrate requirements decrease with aging, and older patients were found to require less cornstarch. Failure to lower the cornstarch doses contributes to over-treatment in adults with GSD Ia. Not only does this lead to worsening hepatomegaly and excessive weight gain, but over-treatment contributes to relative hyperinsulinism and rebound hypoglycemia. This knowledge is essential in designing nutritional therapies for the aging GSD population.

CONFLICT OF INTEREST

K.D., I.F., T.R., G.B., C.-L.K., and P.R. declare that they have no financial conflict of interest. M.D., K.R., and D.W. are all part of the GLYDE study which is an international trial assessing the efficacy of Glycosade extended release cornstarch for daytime use in GSD. D.W. receives grant support from the following companies, but the work is unrelated to this study: Ultragenyx, Generation Bio, and Logic Bio. None of the authors have intellectual property related to glycogen storage disease.

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