Evidence map›Paper›PMID 25804941›Full record

ArticleDiabetes2015

Diabetes Limits Stem Cell Mobilization Following G-CSF but Not Plerixafor.

Gian Paolo Fadini, Mark Fiala, Roberta Cappellari, Marianna Danna, Soo Park, Nicol Poncina, Lisa Menegazzo, Mattia Albiero, John DiPersio, Keith Stockerl-Goldstein and 1 more

Abstract read
In one paragraph

Article in Diabetes, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
5.7field-weighted citation impact, top 4% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Transcriptomic Profile of LinBMC genomics · 2024
    Article
  6. Article
  7. Review
  8. Article
  9. Type 1 diabetes patients increase CXCR4Scientific reports · 2021
    Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Advances in bone marrow stem cell therapy for retinal dysfunction.Progress in retinal and eye research · 2017
    Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 2 countries.

Gian Paolo FadiniDivision of Metabolic Diseases, Department of Medicine, University of Padova, Padova, Italy Laboratory of Experimental Diabetology, Venetian Institute of Molecular Medicine, Padova, Italy gianpaolo.fadini@unipd.it.
Mark FialaDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, MO.
Roberta CappellariLaboratory of Experimental Diabetology, Venetian Institute of Molecular Medicine, Padova, Italy.
Marianna DannaDivision of Metabolic Diseases, Department of Medicine, University of Padova, Padova, Italy.
Soo ParkDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, MO.
Nicol PoncinaDivision of Metabolic Diseases, Department of Medicine, University of Padova, Padova, Italy Laboratory of Experimental Diabetology, Venetian Institute of Molecular Medicine, Padova, Italy.
Lisa MenegazzoDivision of Metabolic Diseases, Department of Medicine, University of Padova, Padova, Italy Laboratory of Experimental Diabetology, Venetian Institute of Molecular Medicine, Padova, Italy.
Mattia AlbieroDivision of Metabolic Diseases, Department of Medicine, University of Padova, Padova, Italy Laboratory of Experimental Diabetology, Venetian Institute of Molecular Medicine, Padova, Italy.
John DiPersioDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, MO.
Keith Stockerl-GoldsteinDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, MO.
Angelo AvogaroDivision of Metabolic Diseases, Department of Medicine, University of Padova, Padova, Italy Laboratory of Experimental Diabetology, Venetian Institute of Molecular Medicine, Padova, Italy.
University of Padua · ITWashington University in St. Louis · USVeneto Institute of Molecular Medicine · IT

Funding

TARGETING AML-STROMAL INTERACTIONSR01CA152329 · NCI · WASHINGTON UNIVERSITY · PI DIPERSIO, JOHN F. · 2011 to 2015
$2.5M
OPTIMIZING ALLOGENEIC TRANSPLANTATION USING CXCR4 BLOCKADER21CA141523 · NCI · WASHINGTON UNIVERSITY · PI DIPERSIO, JOHN F. · 2009 to 2010
$669k
NCI NIH HHS R01 CA152329NCI NIH HHS R01-CA-152329NCI NIH HHS R21 CA141523NCI NIH HHS R21-CA-141523-01
6 · The paper itself

Abstract

Previous studies suggest that diabetes impairs hematopoietic stem cell (HSC) mobilization in response to granulocyte colony-stimulating factor (G-CSF). In this study, we tested whether the CXCR4 antagonist plerixafor, differently from G-CSF, is effective in mobilizing HSCs in patients with diabetes. In a prospective study, individuals with and without diabetes (n = 10/group) were administered plerixafor to compare CD34(+) HSC mobilization; plerixafor was equally able to mobilize CD34(+) HSCs in the two groups, whereas in historical data, G-CSF was less effective in patients with diabetes. In a retrospective autologous transplantation study conducted on 706 patients, diabetes was associated with poorer mobilization in patients who received G-CSF with/without chemotherapy, whereas it was not in patients who received G-CSF plus plerixafor. Similarly in an allogeneic transplantation study (n = 335), diabetes was associated with poorer mobilization in patients who received G-CSF. Patients with diabetes who received G-CSF without plerixafor had a lower probability of reaching >50/μL CD34(+) HSCs, independent from confounding variables. In conclusion, diabetes negatively impacted HSC mobilization after G-CSF with or without chemotherapy but had no effect on mobilization induced by G-CSF with plerixafor. This finding has major implications for the care of patients with diabetes undergoing stem cell mobilization and transplantation and for the vascular regenerative potential of bone marrow stem cells.

Indexed as

Hematopoietic Stem Cell MobilizationAdultBenzylaminesCyclamsDiabetes Mellitus, Type 1FemaleGranulocyte Colony-Stimulating FactorHematopoietic Stem CellsHematopoietic Stem Cell TransplantationHeterocyclic CompoundsHumansMaleMiddle AgedProspective StudiesReceptors, CXCR4Retrospective StudiesBenzylaminesCyclamsGranulocyte Colony-Stimulating FactorHeterocyclic CompoundsplerixaforReceptors, CXCR4

Identifiers

PMID25804941
PMCPMC4512229
OpenAlexW1917663973

What OpenQuestion holds

Textmetadata
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.