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1000 Titel
  • Impact of glycogen storage disease type I on adult daily life: a survey
1000 Autor/in
  1. Garbade, Sven F. |
  2. Ederer, Viviane |
  3. Burgard, Peter |
  4. Wendel, Udo |
  5. Spiekerkoetter, Ute |
  6. Haas, Dorothea |
  7. Grünert, Sarah Catharina |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-09-03
1000 Erschienen in
1000 Quellenangabe
  • 16(1):371
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s13023-021-02006-w |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8414849/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Background!#!Glycogen storage disease type I (GSD I) is a rare autosomal recessive disorder of carbohydate metabolism characterized by recurrent hypoglycaemia and hepatomegaly. Management of GSD I is demanding and comprises a diet with defined carbohydrate intake and the use of complex carbohydrates, nocturnal tube feeding or night-time uncooked cornstarch intake, regular blood glucose monitoring and the handling of emergency situations. With improved treatment, most patients nowadays survive into adulthood. Little research has been performed on the impact of GSD I on daily life, especially in adult patients.!##!Results!#!In this multi-centre study we assessed the impact of GSD I on adult daily life in 34 GSD I patients (27 GSD Ia, 7 GSD Ib) between 17 and 54 years (median 26 years) using a self-designed questionnaire that specifically focused on different aspects of daily life, such as job situation, social life, sports, travelling, composition of the household, night-time and day-time dietary management and disease monitoring as well as the patient's attitude towards the disease. At the time of investigation, the majority of patients either attended school or university or were employed, while 3 patients (9%) were out of work. Most patients ranked GSD I as a disease with moderate severity and disease burden. Dietary treatment was considered challenging by many, but the vast majority of patients considered life with GSD I as well-manageable.!##!Conclusions!#!Although the management of GSD I poses a significant burden on daily life, most patients live an independent adult life, have a positive attitude towards their disease and seem to cope well with their situation.
1000 Sacherschließung
lokal Surveys and Questionnaires [MeSH]
lokal Coping
lokal Inherited metabolic diseases
lokal Adult [MeSH]
lokal Blood Glucose Self-Monitoring [MeSH]
lokal Humans [MeSH]
lokal Glucose-6-phosphatase
lokal Glycogen storage disease type I
lokal Glycogen Storage Disease Type I [MeSH]
lokal Quality of life
lokal Glucose-6-phosphate transporter
lokal Blood Glucose [MeSH]
lokal Research
lokal Hypoglycemia [MeSH]
lokal Disease burden
lokal Glycogen Storage Disease [MeSH]
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/R2FyYmFkZSwgU3ZlbiBGLg==|https://frl.publisso.de/adhoc/uri/RWRlcmVyLCBWaXZpYW5l|https://frl.publisso.de/adhoc/uri/QnVyZ2FyZCwgUGV0ZXI=|https://frl.publisso.de/adhoc/uri/V2VuZGVsLCBVZG8=|https://frl.publisso.de/adhoc/uri/U3BpZWtlcmtvZXR0ZXIsIFV0ZQ==|https://frl.publisso.de/adhoc/uri/SGFhcywgRG9yb3RoZWE=|https://orcid.org/0000-0001-5986-0468
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