Evidence map›Paper›PMID 30451720›Full record

Trial reportCurrent opinion in hematology2019

Neutropenia in glycogen storage disease Ib: outcomes for patients treated with granulocyte colony-stimulating factor.

David C Dale, Audrey Anna Bolyard, Tracy Marrero, Merideth L Kelley, Vahagn Makaryan, Emily Tran, Jamie Leung, Laurence A Boxer, Priya S Kishnani, Stephanie Austin and 8 more

Registry-linked trialOpen access · greenAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Current opinion in hematology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05078879 (A Phase 1 Study of Empagliflozin as Treatment for Severe Congenital Neutropenia Due to G6PC3 Deficiency), which is not on this map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
4.2field-weighted citation impact, top 6% 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.

NCT05078879 phase1completednot on this mapstarted 2021, after this paper: background citation

A Phase 1 Study of Empagliflozin as Treatment for Severe Congenital Neutropenia Due to G6PC3 Deficiency

TypeinterventionalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2021 to 2025Enrolled4ConditionsCrohn's Disease, Glycogen Metabolism, Inflammatory Bowel Disease (IBD)ArmsEmpagliflozin
3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 63 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Gene therapy for glycogen storage diseases.Journal of inherited metabolic disease · 2024
    Review
  12. The metabolic basis of inherited neutropenias.British journal of haematology · 2024
    Review
  13. Review
  14. Glycogen storage diseases: An update.World journal of gastroenterology · 2023
    Review
  15. Review
  16. Article
  17. Review
  18. 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

18 authors at 9 institutions in 3 countries.

David C DaleDivision of GIM, Department of Medicine, University of Washington.
Audrey Anna BolyardDepartment of Medicine, University of Washington, Severe Chronic Neutropenia International Registry, Seattle, Washington.
Tracy MarreroDepartment of Medicine, University of Washington, Severe Chronic Neutropenia International Registry, Seattle, Washington.
Merideth L KelleyDivision of GIM, Department of Medicine, University of Washington.
Vahagn MakaryanDivision of GIM, Department of Medicine, University of Washington.
Emily TranDepartment of Medicine, University of Washington, Severe Chronic Neutropenia International Registry, Seattle, Washington.
Jamie LeungDepartment of Medicine, University of Washington, Severe Chronic Neutropenia International Registry, Seattle, Washington.
Laurence A BoxerPediatric Hematology Oncology, University of Michigan, Ann Arbor, Michigan.
Priya S KishnaniDivision of Medical Genetics, Duke University Medical Center, Durham, North Carolina.
Stephanie AustinDivision of Medical Genetics, Duke University Medical Center, Durham, North Carolina.
Corbinian WannerDepartment of Pediatrics, Glycogen Storage Disease Program, Connecticut Children's Medical Center, Hartford, Connecticut, USA.
Iris A FerrecchiaDepartment of Pediatrics, Glycogen Storage Disease Program, Connecticut Children's Medical Center, Hartford, Connecticut, USA.
Dina KhalafDepartment of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
Dawn MazeDepartment of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
Joanne KurtzbergDepartment of Pediatrics/Pediatric Blood and Marrow Transplantation/Department of Pathology, Duke University Medical Center, Durham, North Carolina, USA.
Cornelia ZeidlerDepartment of Molecular Hematopoiesis, Medizinische Hochschule Hannover, Hannover.
Karl WelteDivision of Hematology/Oncology, Department of Molecular Hematopoiesis, University Children's Hospital of Tuebingen, Tuebingen, Germany.
David A WeinsteinDepartment of Pediatrics, Glycogen Storage Disease Program, Connecticut Children's Medical Center, Hartford, Connecticut, USA.
University of Washington · USConnecticut Children's Medical Center · USDuke Medical Center · USUniversity Health Network · CADuke University · USGTx (United States) · USMedizinische Hochschule Hannover · DEUniversity Children's Hospital Tübingen · DEUniversity of Michigan–Ann Arbor · US

Funding

Severe Chronic Neutropenia International RegistryR24AI049393 · NIAID · UNIVERSITY OF WASHINGTON · PI DALE, DAVID CHANDLER · 2004 to 2019
$10.6M
NIAID NIH HHS R24 AI049393
6 · The paper itself

Abstract

purpose of reviewGlycogen storage disease Ib (GSD Ib) is characterized by hepatomegaly, hypoglycemia, neutropenia, enterocolitis and recurrent bacterial infections. It is attributable to mutations in G6PT1, the gene for the glucose-6-phosphate transporter responsible for transport of glucose into the endoplasmic reticulum. Neutropenia in GSD Ib is now frequently treated with granulocyte colony-stimulating factor (G-CSF). We formed a cooperative group to review outcomes of the long-term treatment of GSD Ib patients treated with G-CSF. RECENT

findingsThe study enrolled 103 patients (48 men and 55 women), including 47 currently adult patients. All of these patients were treated with G-CSF, starting at a median age of 3.8 years (range 0.04-33.9 years) with a median dose of 3.0 mcg/kg/day (range 0.01-93.1 mcg/kg/day) for a median of 10.3 years (range 0.01-29.3 years). Neutrophils increased in response to G-CSF in all patients (median values before G-CSF 0.2 × 10/l, on G-CSF 1.20 x 10/l). Treatment increased spleen size (before G-CSF, 47%, on treatment on G-CSF 76%), and splenomegaly was the dose-limiting adverse effect of treatment (pain and early satiety). Clinical observations and records attest to reduce frequency of infectious events and the severity of inflammatory bowel symptoms, but fever and recurrent infections remain a significant problem. In the cohort of patients followed carefully through the Severe Chronic Neutropenia International Registry, four patients have developed myelodysplasia or acute myeloid leukemia and we are aware of four other cases, (altogether seven on G-CSF, one never treated with G-CSF). Liver transplantation in five patients did not correct neutropenia. Four patients had hematopoietic stem cell transplantation; two adults and two children were transplanted; one adult and one child survived. SUMMARY: GSD Ib is a complex disorder of glucose metabolism causing severe chronic neutropenia. G-CSF is effective to raise blood neutrophil counts and reduce fevers and infections in most patients. In conjunction with other therapies (salicylates, mesalamine sulfasalazine and prednisone), G-CSF ameliorates inflammatory bowel symptoms, but doses must be limited because it increases spleen size associated with abdominal pain.

Indexed as

RegistriesAdolescentAdultChildChild, PreschoolDisease-Free SurvivalFemaleGlycogen Storage Disease Type IGranulocyte Colony-Stimulating FactorHumansMaleMiddle AgedNeutropeniaNeutrophilsSurvival RateGranulocyte Colony-Stimulating Factor

Identifiers

PMID30451720
PMCPMC7000169
OpenAlexW2901657984

What OpenQuestion holds

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Registered trials

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.