Evidence map›Paper›PMID 29931411›Full record

ArticleStem cell reviews and reports2018

CD34+ Hematopoietic Stem Cell Count Is Predictive of Vascular Event Occurrence in Children with Sickle Cell Disease.

Manoelle Kossorotoff, Mariane De Montalembert, Valentine Brousse, Dominique Lasne, Emmanuel Curis, David M Smadja, Romaric Lacroix, Sebastien Bertil, Elodie Masson, Isabelle Desguerre and 2 more

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In one paragraph

Article in Stem cell reviews and reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 48% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

12 authors at 4 institutions in 1 country.

Manoelle KossorotoffInserm UMR-S1140, Faculté de Pharmacie, Paris, France. manoelle.kossorotoff@aphp.fr.ORCID 0000-0002-0813-9045
Mariane De MontalembertAP-HP, Pediatric Sickle Cell Clinic, Hôpital Universitaire Necker-Enfants malades and Laboratory of Excellence, GR-Ex, Paris, France.
Valentine BrousseAP-HP, Pediatric Sickle Cell Clinic, Hôpital Universitaire Necker-Enfants malades and Laboratory of Excellence, GR-Ex, Paris, France.
Dominique LasneInserm UMR-S1140, Faculté de Pharmacie, Paris, France.
Emmanuel CurisSorbonne Paris Cité, Université Paris Descartes, Paris, France.
David M SmadjaInserm UMR-S1140, Faculté de Pharmacie, Paris, France.
Romaric LacroixInserm UMR-S1076, UFR de Pharmacie, Aix Marseille Université, Marseille, France.
Sebastien BertilAP-HP, Service d'hématologie biologique, Hôpital Européen Georges Pompidou, Paris, France.
Elodie MassonInserm UMR-S1076, UFR de Pharmacie, Aix Marseille Université, Marseille, France.
Isabelle DesguerreAP-HP, Child Neurology, French center for pediatric stroke, Hôpital Universitaire Necker-Enfants malades, 149 rue de Sèvres, 75015, Paris, France.
Damien BonnetSorbonne Paris Cité, Université Paris Descartes, Paris, France.
Pascale GaussemInserm UMR-S1140, Faculté de Pharmacie, Paris, France.
Délégation Paris 5 · FRHôpital Necker-Enfants Malades · FRInserm · FRAssistance Publique – Hôpitaux de Paris · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectivesSickle cell disease (SCD) complications mostly result from vascular dysfunction, concerning systemic microvasculature and cerebral large vessels. The aim of this cohort study was to identify potential circulating biomarkers predictive for further vascular event occurrence in pediatric SCD.

methodsWe consecutively enrolled 108 children with SCD at steady state, aged 3-18 years old (median 9.8 years). Hematology, coagulation, hemolysis, endothelial, platelet and vascular activation parameters were recorded at inclusion. Neurovascular and systemic vascular events were prospectively recorded during a mean follow-up period of 27 months.

resultsPatients at steady state displayed significantly higher hemolysis and platelet activation markers, higher leukocyte, CD34+ hematopoietic stem cell and microvesicle counts, and a pro-coagulant profile compared to controls matched for age and ethnicity. Circulating endothelial cell or nucleosome level did not differ. During the follow-up period, 36 patients had at least one neurovascular (n = 12) or systemic vascular event (n = 25). In a multivariate model, high CD34+ cell count was the best predictor for the occurrence of a vascular event (OR 1.2 for 1000 cell/mL increase, 95% CI [1.049-1.4], p = 0.013, sensitivity 53%, specificity 84% for a threshold of 8675 cells/mL).

conclusionCD34+ cell count at steady state is a promising biomarker of further vascular event in children with SCD.

Indexed as

AdolescentAnemia, Sickle CellAntigens, CD34BiomarkersBlood PlateletsBlood VesselsCell-Derived MicroparticlesCerebellumChildChild, PreschoolFemaleHematopoietic Stem CellsHumansMaleAntigens, CD34BiomarkersCD34+ hematopoietic stem cellChildrenPrognostic factorsSickle-cell diseaseStrokeVascular disease

Identifiers

PMID29931411
OpenAlexW2808761584

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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.