Evidence map›Paper›PMID 32300528›Full record

ArticleMolecular genetics and metabolism reports2020

Infectious and digestive complications in glycogen storage disease type Ib: Study of a French cohort.

Camille Wicker, Célina Roda, Ariane Perry, Jean Baptiste Arnoux, Anais Brassier, Martin Castelle, Aude Servais, Jean Donadieu, Juliette Bouchereau, Bénédicte Pigneur and 3 more

Open access · goldAbstract read
In one paragraph

Article in Molecular genetics and metabolism reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.6field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. [Efficacy and safety of empagliflozin in the treatment of glycogen storage disease-associated inflammatory bowel disease].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2025
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Glycogen storage diseases: An update.World journal of gastroenterology · 2023
    Review
  13. Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. [Inherited metabolic liver disease-associated infection].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2021
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 6 institutions in 1 country.

Camille WickerReference Center for Inherited Metabolic Diseases, Necker Hospital, APHP, Filière G2 M, MetabERN, Paris, France.
Célina RodaParis University, CRESS, HERA (Health Environmental Risk Assessment) team, INSERM, INRA, F-75004 Paris, France.
Ariane PerryReference Center for Inherited Metabolic Diseases, Antoine Béclère Hospital, APHP, Filière G2M, MetabERN, Clamart, France.
Jean Baptiste ArnouxReference Center for Inherited Metabolic Diseases, Necker Hospital, APHP, Filière G2 M, MetabERN, Paris, France.
Anais BrassierReference Center for Inherited Metabolic Diseases, Necker Hospital, APHP, Filière G2 M, MetabERN, Paris, France.
Martin CastelleHematology, Necker Hospital, APHP, Paris Descartes University, Paris, France.
Aude ServaisReference Center for Inherited Metabolic Diseases, Necker Hospital, APHP, Filière G2 M, MetabERN, Paris, France.
Jean DonadieuHematology Department, Trousseau Hospital, APHP, Paris, France.
Juliette BouchereauReference Center for Inherited Metabolic Diseases, Necker Hospital, APHP, Filière G2 M, MetabERN, Paris, France.
Bénédicte PigneurPaediatric Gastroentérology Department, Necker Hospital, APHP, Paris, France.
Philippe LabruneReference Center for Inherited Metabolic Diseases, Antoine Béclère Hospital, APHP, Filière G2M, MetabERN, Clamart, France.
Frank M RuemmelePaediatric Gastroentérology Department, Necker Hospital, APHP, Paris, France.
Pascale de LonlayReference Center for Inherited Metabolic Diseases, Necker Hospital, APHP, Filière G2 M, MetabERN, Paris, France.
Assistance Publique – Hôpitaux de Paris · FRHôpital Necker-Enfants Malades · FRInserm · FRUniversité Paris Cité · FRUniversité Paris-Saclay · FRUniversité Paris-Sud · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glycogenosis type Ib (GSD1B) causes not only hypoglycemia but also infections and "Crohn's disease like" inflammatory bowel disease (IBD) that can significantly impair patient's quality of life. We retrospectively evaluated infectious and digestive complications in 9 French patients (3 girls, 6 boys) diagnosed at 0.8 years on average, with a mean follow-up of 19.1 years. Infections occurred earlier than IBD, at mean ages of 1.7 and 3.8 years, respectively. The number of acute hospitalizations was 0.7/year due to infectious (0.4/year) or digestive symptoms (0.4/year). Clinical presentations allowed separating patients into mild (

Indexed as

ANC, Absolute Neutrophil CountAnti-inflammatory solutionsCD, Crohn's diseaseCRP, C-reactive proteinEEN, Exclusive Enteral NutritionEN, Enteral NutritionENT, Ear, Nose and ThroatESR, erythrocyte sedimentation rateG6PT, glucose-6-phosphate translocaseG-CSF, Granulocyte colony-stimulating factorGlycogen storage disease type 1BGSD1, Glycogen storage disease type IHarvey Bradshaw scoreIBD, Inflammatory Bowel DiseaseInflammatory bowel diseaseNeutropeniaPEN, Partial Enteral NutritionSD, Standard Deviation

Identifiers

PMID32300528
PMCPMC7152669
OpenAlexW3015807439

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.