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Dietary lipids in glycogen storage disease type III: A systematic literature study, case studies, and future recommendations.

Publication ,  Journal Article
Rossi, A; Hoogeveen, IJ; Bastek, VB; de Boer, F; Montanari, C; Meyer, U; Maiorana, A; Bordugo, A; Dianin, A; Campana, C; Rigoldi, M; Parini, R ...
Published in: J Inherit Metab Dis
July 2020

A potential role of dietary lipids in the management of hepatic glycogen storage diseases (GSDs) has been proposed, but no consensus on management guidelines exists. The aim of this study was to describe current experiences with dietary lipid manipulations in hepatic GSD patients. An international study was set up to identify published and unpublished cases describing hepatic GSD patients with a dietary lipid manipulation. A literature search was performed according to the Cochrane Collaboration methodology through PubMed and EMBASE (up to December 2018). All delegates who attended the dietetics session at the IGSD2017, Groningen were invited to share unpublished cases. Due to multiple biases, only data on GSDIII were presented. A total of 28 cases with GSDIII and a dietary lipid manipulation were identified. Main indications were cardiomyopathy and/or myopathy. A high fat diet was the most common dietary lipid manipulation. A decline in creatine kinase concentrations (n = 19, P < .001) and a decrease in cardiac hypertrophy in paediatric GSDIIIa patients (n = 7, P < .01) were observed after the introduction with a high fat diet. This study presents an international cohort of GSDIII patients with different dietary lipid manipulations. High fat diet may be beneficial in paediatric GSDIIIa patients with cardiac hypertrophy, but careful long-term monitoring for potential complications is warranted, such as growth restriction, liver inflammation, and hepatocellular carcinoma development.

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Published In

J Inherit Metab Dis

DOI

EISSN

1573-2665

Publication Date

July 2020

Volume

43

Issue

4

Start / End Page

770 / 777

Location

United States

Related Subject Headings

  • Triglycerides
  • Monitoring, Physiologic
  • Liver
  • Humans
  • Glycogen Storage Disease Type III
  • Genetics & Heredity
  • Dietary Fats
  • Child
  • Cardiomyopathies
  • 3202 Clinical sciences
 

Citation

APA
Chicago
ICMJE
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Rossi, A., Hoogeveen, I. J., Bastek, V. B., de Boer, F., Montanari, C., Meyer, U., … Derks, T. G. J. (2020). Dietary lipids in glycogen storage disease type III: A systematic literature study, case studies, and future recommendations. J Inherit Metab Dis, 43(4), 770–777. https://doi.org/10.1002/jimd.12224
Rossi, Alessandro, Irene J. Hoogeveen, Vanessa B. Bastek, Foekje de Boer, Chiara Montanari, Uta Meyer, Arianna Maiorana, et al. “Dietary lipids in glycogen storage disease type III: A systematic literature study, case studies, and future recommendations.J Inherit Metab Dis 43, no. 4 (July 2020): 770–77. https://doi.org/10.1002/jimd.12224.
Rossi A, Hoogeveen IJ, Bastek VB, de Boer F, Montanari C, Meyer U, et al. Dietary lipids in glycogen storage disease type III: A systematic literature study, case studies, and future recommendations. J Inherit Metab Dis. 2020 Jul;43(4):770–7.
Rossi, Alessandro, et al. “Dietary lipids in glycogen storage disease type III: A systematic literature study, case studies, and future recommendations.J Inherit Metab Dis, vol. 43, no. 4, July 2020, pp. 770–77. Pubmed, doi:10.1002/jimd.12224.
Rossi A, Hoogeveen IJ, Bastek VB, de Boer F, Montanari C, Meyer U, Maiorana A, Bordugo A, Dianin A, Campana C, Rigoldi M, Kishnani PS, Pendyal S, Strisciuglio P, Gasperini S, Parenti G, Parini R, Paci S, Melis D, Derks TGJ. Dietary lipids in glycogen storage disease type III: A systematic literature study, case studies, and future recommendations. J Inherit Metab Dis. 2020 Jul;43(4):770–777.
Journal cover image

Published In

J Inherit Metab Dis

DOI

EISSN

1573-2665

Publication Date

July 2020

Volume

43

Issue

4

Start / End Page

770 / 777

Location

United States

Related Subject Headings

  • Triglycerides
  • Monitoring, Physiologic
  • Liver
  • Humans
  • Glycogen Storage Disease Type III
  • Genetics & Heredity
  • Dietary Fats
  • Child
  • Cardiomyopathies
  • 3202 Clinical sciences