Evidence map›Paper›PMID 30451719›Full record

Trial reportCurrent opinion in hematology2019

Neutropenia in Barth syndrome: characteristics, risks, and management.

Colin G Steward, Sarah J Groves, Carolyn T Taylor, Melissa K Maisenbacher, Birgitta Versluys, Ruth A Newbury-Ecob, Hulya Ozsahin, Michaela K Damin, Valerie M Bowen, Katherine R McCurdy and 3 more

Open 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. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

31 citing papers in PubMed, 54 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Cardiolipin preserves TNature metabolism · 2026
    Article
  5. Article
  6. Article
  7. Effects of Cannabidiol on TAFAZZIN-Deficient B-Lymphoblastoid Cells.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  8. Mitochondrial Transplantation as a Therapeutic Strategy for Inherited Mitochondrial Diseases.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  9. Review
  10. Review
  11. Article
  12. Mitochondria-Homing Drug Mitochonic Acid 5 Improves Barth Syndrome Myopathy in a Human-Induced Pluripotent Stem Cell Model and Barth Syndrome Drosophila Model.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  13. Article
  14. Barth Syndrome:Genes · 2025
    Review
  15. The metabolic basis of inherited neutropenias.British journal of haematology · 2024
    Review
  16. Review
  17. Article
  18. Review
  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 10 institutions in 5 countries.

Colin G StewardNHS Specialised Services Barth Syndrome Service, Royal Hospital for Children.
Sarah J GrovesSchool of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.
Carolyn T TaylorDepartment of Pediatrics, Division of Cardiology, Children's Hospital, Medical University of South Carolina, Charleston, South Carolina.
Melissa K MaisenbacherNatera, San Carlos, California, USA.
Birgitta VersluysDepartment of Immunology/Hematology and BMT, University Medical Center Utrecht, Utrecht, The Netherlands.
Ruth A Newbury-EcobDepartment of Clinical Genetics, St Michael's Hospital, Bristol, UK.
Hulya OzsahinFormer: University Children's Hospital, Geneva.
Michaela K DaminBarth Syndrome Trust, Romsey, UK.
Valerie M BowenBarth Syndrome Foundation, Inc., Larchmont, New York, USA.
Katherine R McCurdyBarth Syndrome Foundation, Inc., Larchmont, New York, USA.
Michael C MackeyDepartments of Physiology, Physics, and Mathematics, Centre for Applied Mathematics in Bioscience and Medicine, McGill University, Montreal, Québec, Canada.
Audrey A BolyardSevere Chronic Neutropenia International Registry.
David C DaleDepartment of Medicine, University of Washington, Seattle, Washington, USA.
Barth Syndrome Foundation · USMcGill University · CAMedical University of South Carolina · USNatera (United States) · USRoyal Hospital for Children · GBSt Michael's Hospital · GBSwissmedic · CHUniversity Medical Center Utrecht · NLUniversity of Bristol · GBUniversity of Washington · 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 reviewBarth syndrome (BTHS) is an X-linked disease characterized by defective remodeling of phospholipid side chains in mitochondrial membranes. Major features include neutropenia, dilated cardiomyopathy, motor delay and proximal myopathy, feeding problems, and constitutional growth delay. We conducted this review of neutropenia in BTHS to aid in the diagnosis of this disease, and to improve understanding of both the consequences of neutropenia and the benefits of treatment with granulocyte colony-stimulating factor (G-CSF). RECENT

findingsIn 88 patients with BTHS, neutropenia, that is, at least one count below 1.5 × 10/l, was detected in 74 (84%) and 44% had severe chronic neutropenia, with multiple counts below 0.5 × 10/l. The pattern of neutropenia varied between intermittent and unpredictable, chronic and severe, or cyclical with mathematically regular oscillations. Monocytosis, that is, monocytes more than 1.0 × 10/l, was observed at least once in 64 of 85 (75%) patients. G-CSF was administered to 39 of 88 patients (44%). Weekly average G-CSF doses ranged from 0.12 to 10.92 μg/kg/day (mean 1.16 μg/kg/day, median 1.16 μg/kg/day). Antibiotic prophylaxis was additionally employed in 21 of 26 neutropenic patients. Pretreatment bone marrow evaluations predominantly showed reduced myeloid maturation which normalized on G-CSF therapy in seven of 13 examined. Consistent clinical improvement, with reduced signs and symptoms of infections, was observed in response to prophylactic G-CSF ± prophylactic antibiotics. However, despite G-CSF and antibiotics, one adult patient died with multiple infections related to indwelling medical devices and gastrostomy site infection after 15.5 years on G-CSF and a pediatric patient required gastrostomy removal for recurrent abdominal wall cellulitis. SUMMARY: BTHS should be considered in any men with neutropenia accompanied by any of the characteristic features of this syndrome. Prophylaxis with G-CSF ± antibiotics prevents serious bacterial infections in the more severe neutropenic patients although infections remain a threat even in patients who are very compliant with therapy, especially in those with indwelling devices.

Indexed as

Anti-Bacterial AgentsBarth SyndromeBone MarrowGranulocyte Colony-Stimulating FactorHumansLeukocyte CountMaleRisk FactorsAnti-Bacterial AgentsGranulocyte Colony-Stimulating Factor

Identifiers

PMID30451719
PMCPMC6392059
OpenAlexW2900714311

What OpenQuestion holds

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Registered trials

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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.