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Alternative nighttime nutrition regimens in glycogen storage disease type I: a controlled crossover study

  • Original Article
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Journal of Inherited Metabolic Disease

Abstract

Background

Traditional approaches for nighttime glycemic control in glycogen storage disease type I (GSDI) include continuous tube feeding, or ingestion of uncooked corn starch (CS) at bedtime. A modified corn starch (MCS) has been shown to prolong euglycemia in some patients. The aim of this study was to evaluate whether stable nighttime glucose control can be achieved with other types of slowly digested carbohydrates in adult GSDI patients.

Methods

In this cross-over study, nocturnal glucose control and fasting times were assessed with three different nocturnal nutrition regimens in five patients, using continuous glucose monitoring (CGMS) in an outpatient everyday life setting. For each patient, continuous glucose profiles were measured after ingestion of (1) CS, (2) MCS or (3) a pasta meal at bedtime, during 5 to 6 consecutive nights for each regimen.

Results

Stable nocturnal glucose control was achieved for all patients with a pasta meal, with a mean duration of glycemia >3.5 mmol/l of 7.6 h (range 5.7-10.8), and >4 mmol/l of 7 h (5.2-9.2), similar to CS and MCS. Fasting glucose before breakfast on workdays (after 7.1 ± 0.8 h) was not significantly different between the three interventions (CS 4.1 ± 0.5 mmol/l, MCS 4.6 ± 0.7 mmol/l, pasta 4.3 ± 0.9 mmol/l). During prolonged fasting on weekends, longer duration of normoglycemia was achieved with CS or MCS than with pasta.

Conclusion

Consumption of cooked pasta is a suitable and more palatable alternative to uncooked corn starch to achieve nighttime glucose control in adult patients with GSDI.

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References

  • Aravind N, Sissons M, Fellows CM, Blazek J, Gilbert EP (2013) Optimisation of resistant starch II and III levels in durum wheat pasta to reduce in vitro digestibility while maintaining processing and sensory characteristics. Food Chem 136:1100–1109

    Article  CAS  PubMed  Google Scholar 

  • Bhattacharya K (2011) Dietary dilemmas in the management of glycogen storage disease type I. J Inherit Metab Dis 34:621–629

    Article  CAS  PubMed  Google Scholar 

  • Bhattacharya K, Orton RC, Qi X et al (2007) A novel starch for the treatment of glycogen storage diseases. J Inherit Metab Dis 30:350–357

    Article  CAS  PubMed  Google Scholar 

  • Bjorck I, Granfeldt Y, Liljeberg H, Tovar J, Asp NG (1994) Food properties affecting the digestion and absorption of carbohydrates. Am J Clin Nutr 59:699s–705s

    CAS  PubMed  Google Scholar 

  • Chen Y-T, Kishnani PS, Koeberl D (2013) Glycogen storage diseases. In: Beaudet AL, Vogelstein B, Kinzler KW et al (eds) The online metabolic and molecular bases of inherited disease New York. The McGraw-Hill Companies, Inc., NY

    Google Scholar 

  • Chou JY, Jun HS, Mansfield BC (2010) Glycogen storage disease type I and G6Pase-beta deficiency: etiology and therapy. Nat Rev Endocrinol 6:676–688

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Correia CE, Bhattacharya K, Lee PJ et al (2008) Use of modified cornstarch therapy to extend fasting in glycogen storage disease types Ia and Ib. Am J Clin Nutr 88:1272–1276

    PubMed Central  CAS  PubMed  Google Scholar 

  • Fardet A, Abecassis J, Hoebler C et al (1999) Influence of technological modifications of the protein network from pasta on in vitro starch degradation. J Cereal Sci 30:133–145

    Article  CAS  Google Scholar 

  • Kasapkara CS, Cinasal Demir G, Hasanoglu A, Tumer L (2014) Continuous glucose monitoring in children with glycogen storage disease type I. Eur J Clin Nutr 68:101–105

    Article  CAS  PubMed  Google Scholar 

  • Kishnani PS, Austin SL, Abdenur JE et al (2014) Diagnosis and management of glycogen storage disease type I: a practice guideline of the American College of Medical Genetics and Genomics. Genet Med : Off J Am Coll Med Genet 16, e1

    CAS  Google Scholar 

  • Rake JP, Visser G, Labrune P et al (2002) Guidelines for management of glycogen storage disease type I - European Study on Glycogen Storage Disease Type I (ESGSD I). Eur J Pediatr 161(Suppl 1):S112–S119

    Article  PubMed  Google Scholar 

  • Riva M, Fessas D, Schiraldi A (2000) Starch retrogradation in cooked pasta and rice. Cereal Chem 77:433–438

    Article  CAS  Google Scholar 

  • Senn S (2002) Crossover trials in clinical research. Wiley Publishing, Chichester

    Book  Google Scholar 

  • Shah KK, O'Dell SD (2013) Effect of dietary interventions in the maintenance of normoglycaemia in glycogen storage disease type 1a: a systematic review and meta-analysis. J Hum Nutr Diet : Off J Br Diet Assoc 26:329–339

    Article  CAS  Google Scholar 

  • Weinstein DA, Wolfsdorf JI (2002) Effect of continuous glucose therapy with uncooked cornstarch on the long-term clinical course of type 1a glycogen storage disease. Eur J Pediatr 161(Suppl 1):S35–S39

    Article  CAS  PubMed  Google Scholar 

  • White FJ, Jones SA (2011) The use of continuous glucose monitoring in the practical management of glycogen storage disorders. J Inherit Metab Dis 34:631–642

    Article  CAS  PubMed  Google Scholar 

  • Wiesli P, Brandle M, Schwegler B, Lehmann R, Spinas GA, Schmid C (2002) A plasma glucose concentration below 2.5 mmol L-1 is not an appropriate criterion to end the 72-h fast. J Intern Med 252:504–509

    Article  CAS  PubMed  Google Scholar 

  • Wolever TM, Jenkins DJ, Kalmusky J et al (1986) Glycemic response to pasta: effect of surface area, degree of cooking, and protein enrichment. Diabetes Care 9:401–404

    Article  CAS  PubMed  Google Scholar 

  • Wolfsdorf JI, Crigler JF Jr (1997) Cornstarch regimens for nocturnal treatment of young adults with type I glycogen storage disease. Am J Clin Nutr 65:1507–1511

    CAS  PubMed  Google Scholar 

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Acknowledgments

This work was supported by ‘radiz – Rare Disease Initiative Zurich, Clinical Research Priority Program University of Zurich’. The authors thank patients for participation in this study. We thank Claudia Morach for dietetic advice and instruction of patients, and Ilona Kehret for the help in glucose sensor instruction.

Conflict of interest

Michel Hochuli, Emanuel Christ, Fabian Meienberg, Roger Lehmann, Jan Krützfeldt and Matthias Baumgartner declare that they have no conflict of interest.

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Correspondence to Michel Hochuli.

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Communicated by: Robin Lachmann

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Hochuli, M., Christ, E., Meienberg, F. et al. Alternative nighttime nutrition regimens in glycogen storage disease type I: a controlled crossover study. J Inherit Metab Dis 38, 1093–1098 (2015). https://doi.org/10.1007/s10545-015-9864-2

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  • DOI: https://doi.org/10.1007/s10545-015-9864-2

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