Evidence map›Paper›PMID 42562797›Full record

ArticleBritish journal of haematology2026

Identification of predictive factors for reversal of cerebral vasculopathy in an original longitudinal cohort study in newborns with sickle cell anaemia.

Julie Sommet, Priscilla Boizeau, Zinedine Haouari, Berengère Koehl, Monique Elmaleh, Emmanuelle Lesprit, Florence Missud, Ghislaine Ithier, Laurent Holvoet, Valentine Brousse and 7 more

Abstract read
PubMed Publisher
In one paragraph

Article in British journal of haematology, 2026. 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
–field-weighted citation impact
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.

  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

17 authors.

Julie SommetINSERM, U 1123 ECEVE Robert-Debré University Hospital, Paris, France.ORCID https://orcid.org/0000-0002-9167-6836
Priscilla BoizeauINSERM, U 1123 ECEVE Robert-Debré University Hospital, Paris, France.ORCID https://orcid.org/0000-0003-4573-4617
Zinedine HaouariAP-HP, Robert-Debré University Hospital, Sickle Cell Disease Reference Centre, Paris, France.ORCID https://orcid.org/0000-0002-9636-4305
Berengère KoehlAP-HP, Robert-Debré University Hospital, Sickle Cell Disease Reference Centre, Paris, France.ORCID https://orcid.org/0000-0001-7087-7199
Monique ElmalehRadiology Department, AP-HP, Robert-Debré University Hospital, Paris, France.ORCID https://orcid.org/0000-0001-8190-8202
Emmanuelle LespritEtablissement Français du Sang, Robert-Debré University Hospital, Paris, France.ORCID https://orcid.org/0009-0006-7316-434X
Florence MissudAP-HP, Robert-Debré University Hospital, Sickle Cell Disease Reference Centre, Paris, France.ORCID https://orcid.org/0009-0007-5887-5300
Ghislaine IthierAP-HP, Robert-Debré University Hospital, Sickle Cell Disease Reference Centre, Paris, France.ORCID https://orcid.org/0009-0004-1835-5595
Laurent HolvoetAP-HP, Robert-Debré University Hospital, Sickle Cell Disease Reference Centre, Paris, France.ORCID https://orcid.org/0009-0007-3430-2487
Valentine BrousseAP-HP, Robert-Debré University Hospital, Sickle Cell Disease Reference Centre, Paris, France.ORCID https://orcid.org/0000-0002-4984-754X
Christophe DelclauxUniversité Paris Cité, AP-HP, Hôpital Robert Debré, Service de Physiologie Pédiatrique-Centre du Sommeil, INSERM NeuroDiderot, Paris, France.ORCID https://orcid.org/0000-0003-2786-0812
André DenjeanUniversité Paris Cité, AP-HP, Hôpital Robert Debré, Service de Physiologie Pédiatrique-Centre du Sommeil, INSERM NeuroDiderot, Paris, France.ORCID https://orcid.org/0009-0008-6616-3271
Suzanne VerlhacRadiology Department, AP-HP, Robert-Debré University Hospital, Paris, France.ORCID https://orcid.org/0000-0003-0449-2607
Corinne AlbertiINSERM, U 1123 ECEVE Robert-Debré University Hospital, Paris, France.ORCID https://orcid.org/0000-0002-9336-1395
André BaruchelPaediatric Haematology-Immunology Department, AP-HP, Robert-Debré University Hospital, Paris, France.ORCID https://orcid.org/0000-0003-0120-6089
Nathalie CouqueMolecular Genetics Department, AP-HP, Robert Debré University Hospital, Paris, France.ORCID https://orcid.org/0000-0002-5109-0857
Malika BenkerrouINSERM, U 1123 ECEVE Robert-Debré University Hospital, Paris, France.ORCID https://orcid.org/0000-0003-4462-8206

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cerebral macrovasculopathy (CV) is a major complication in children with sickle cell anaemia (SCA) and usually requires a long-term transfusion programme (TP) to prevent stroke. This study aimed to identify factors predicting reversal of CV on TP in a single-centre newborn cohort. Among 375 patients, 50 presented CV and received TP. Median age at diagnosis was 4.9 years [3.6-6.1], with median follow-up of 13.3 years (915 patient-years). Transcranial Doppler (TCD) velocities and magnetic resonance angiography (MRA) normalised in 35 patients, that is, they had reversal of CV (RCV group). Fifteen patients had no reversal of CV (No-RCV group). Kaplan-Meier analysis estimated that 48% (95% confidence interval [CI] [33-62]) still had abnormal TCD and/or MRA 5 years after diagnosis. In a multivariate Cox model, three baseline factors independently predicted CV reversal: age at CV onset, initial severity of stenosis and bronchial obstruction. Older age at diagnosis increased the likelihood of CV reversal (hazard ratio [HR] 1.31 per year, 95% CI [1.08-1.59], p = 0.01). In contrast, severe stenosis (HR 0.72 per 10% increase, 95% CI [0.62-0.85], p < 0.0001) and bronchial obstruction (HR 0.14, 95% CI [0.03-0.63], p = 0.001) reduced the likelihood of CV reversal. These results suggest that, beyond TP, managing bronchial obstruction may improve vascular outcomes.

Indexed as

Anemia, Sickle CellCerebrovascular DisordersBlood TransfusionChildChild, PreschoolCohort StudiesFemaleFollow-Up StudiesHumansInfant, NewbornLongitudinal StudiesMagnetic Resonance AngiographyMalePrognosisUltrasonography, Doppler, Transcranialbronchial obstructioncerebrovascular diseasechildrensickle cell anaemiatransfusion programme

Identifiers

PMID42562797

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.