Journal of Inherited Metabolic Disease

, Volume 41, Issue 6, pp 911–912 | Cite as

Next-generation glycogen storage diseases

  • Terry G. J. DerksEmail author
  • Maaike H. Oosterveer
  • Carolina F. De Souza
Open Access

The glycogen storage diseases (GSD) are amongst the earliest recognized inborn errors of metabolism. After the Fulda Workshop on Glycogen Storage Disease (GSD) type I in 1990, international GSD conferences have been held in Fulda (2000), Milan (2010), Lyon (2012), and Heidelberg (2013). Since the start of the internet era, parent-led patient organizations have pushed for international guidelines for treatment and follow-up (Phillips 2002). Subsequent international collaborative cohort studies have defined the phenotypes of GSDs and facilitated the development of internationally agreed clinical guidelines. This special edition of the Journal of Inherited Metabolic Disease discusses highlights of the International GSD conference held at the University Medical Center Groningen, the Netherlands, between 15 and 17 June 2017 (IGSD2017). Fifty-three oral presentations, 52 posters, 11 networking sessions, and 2 “Meet the Expert” sessions attended by 406 participants from 36 countries reflected the recent progress in individualized and novel therapies, monitoring, and empowerment for patients with muscle- and/or liver-specific GSD types.

To foster the involvement of all stakeholders, including parents, in setting the future research agenda, the International Liver Glycogen Storage Disease Priority Setting Partnership (IGSD-PSP) ( was initiated during the IGSD2017 conference, in collaboration with the James Lind Alliance ( This partnership aims to identify and prioritize research addressing current uncertainties about the effects of care and management. The IGSD-PSP is the first international, multi-lingual PSP for a group of ultra-rare disorders. The steering group expects to present the results at the end of 2019.

A highlight of IGSD2017 was the plenary session on gene therapy, including longitudinal results after gene therapy in canine GSD Ia models. Ideally, GSD Ia patients would be no longer dependent on intensive and unsafe (nocturnal) dietary management after a single dose of gene therapy. To date, longitudinal, in vivo functional studies of glucose metabolism in animal models after gene therapy are lacking. Case histories of “mild” GSD Ia patients have demonstrated that episodes of hypoglycemia can remain undiagnosed until patients present with liver adenomas, indirectly emphasizing the importance of determining that exogenously administered genes are stably expressed. Longitudinal monitoring of GSD Ia patients after gene therapy may include a combination of (1) assessment of microsomal glucose-6-phosphatase activities ex vivo (necessitating invasive liver biopsies), (2) execution of (invasive, clinical) fasting challenges in vivo, (3) advanced continuous glucose monitoring in the home situation, and (4) application of stable isotope methods to longitudinally quantify endogenous glucose production rates in vivo (van Dijk et al. 2013).

We are delighted to present this special collection of papers about GSD. Ultra-rare inborn errors of metabolism do not stop at borders between countries or continents and global collaborations are essential. Clinical expertise, secure eHealth applications, active patient participation, and transparent governance structures including all important stakeholders will be fundamental to improving cross border transfer of knowledge, care, and cure between professionals and patients, in all possible directions.


Compliance with ethical standards

Conflict of interest

T.G.J. Derks, M.H. Oosterveer, and C.F. De Souza declare that they have no conflict of interest.


  1. Phillips A (2002) More questions: 10 years later from glycogen storage disease patient support groups in Europe. Eur J Pediatr 161(S1):102–105Google Scholar
  2. van Dijk TH, Laskewitz AJ, Grefhorst A et al (2013) A novel approach to monitor glucose metabolism using stable isotopically labelled glucose in longitudinal studies in mice. Lab Anim 47(2):79–88CrossRefGoogle Scholar

Copyright information

© The Author(s) 2018

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Authors and Affiliations

  • Terry G. J. Derks
    • 1
    Email author
  • Maaike H. Oosterveer
    • 2
  • Carolina F. De Souza
    • 3
  1. 1.Section of Metabolic Diseases, Beatrix Children’s HospitalUniversity Medical Center of Groningen, University of GroningenGroningenThe Netherlands
  2. 2.Department of Pediatrics, Center for Liver Digestive and Metabolic DiseasesUniversity Medical Center Groningen, University of GroningenGroningenThe Netherlands
  3. 3.Medical Genetics ServiceHospital de Clínicas de Porto AlegrePorto AlegreBrazil

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