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

dc.contributor.author

Dale, David C

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Bolyard, Audrey Anna

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Marrero, Tracy

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Kelley, Merideth L

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Makaryan, Vahagn

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Tran, Emily

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Leung, Jamie

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Boxer, Laurence A

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Kishnani, Priya S

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Austin, Stephanie

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Wanner, Corbinian

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Ferrecchia, Iris A

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Khalaf, Dina

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Maze, Dawn

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Kurtzberg, Joanne

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Zeidler, Cornelia

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Welte, Karl

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Weinstein, David A

dc.date.accessioned

2022-03-23T15:18:13Z

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2022-03-23T15:18:13Z

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2019-01

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2022-03-23T15:18:13Z

dc.description.abstract

Purpose of review

Glycogen 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 findings

The 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.
dc.identifier.issn

1065-6251

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1531-7048

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https://hdl.handle.net/10161/24583

dc.language

eng

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Ovid Technologies (Wolters Kluwer Health)

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Current opinion in hematology

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10.1097/moh.0000000000000474

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Neutrophils

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Humans

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Neutropenia

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Glycogen Storage Disease Type I

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Granulocyte Colony-Stimulating Factor

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Disease-Free Survival

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Registries

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Survival Rate

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Adolescent

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Adult

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Middle Aged

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Child

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Child, Preschool

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Female

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Male

dc.title

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

dc.type

Journal article

duke.contributor.orcid

Kishnani, Priya S|0000-0001-8251-909X

duke.contributor.orcid

Kurtzberg, Joanne|0000-0002-3370-0703

pubs.begin-page

16

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21

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1

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Duke

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School of Medicine

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Basic Science Departments

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Clinical Science Departments

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Institutes and Centers

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Molecular Genetics and Microbiology

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Pathology

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Pediatrics

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Pediatrics, Medical Genetics

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Duke Cancer Institute

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Duke Clinical Research Institute

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Institutes and Provost's Academic Units

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Initiatives

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Duke Innovation & Entrepreneurship

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Pediatrics, Transplant and Cellular Therapy

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Published

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26

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