Evidence map›Paper›PMID 34850378›Full record

ArticleBritish journal of haematology2022

Longitudinal assessment of adhesion to vascular cell adhesion molecule-1 at steady state and during vaso-occlusive crises in sickle cell disease.

Jennell White, Michael U Callaghan, Xiufeng Gao, Ke Liu, Ahmar Zaidi, Michael Tarasev, Patrick C Hines

Open access · hybridAbstract read
In one paragraph

Article in British journal of haematology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. Optimizing the right time to start sickle cell therapies.Hematology. American Society of Hematology. Education Program · 2025
    Review
  2. Article
  3. Stratification of βAntioxidants (Basel, Switzerland) · 2023
    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

7 authors at 2 institutions in 1 country.

Jennell WhiteDepartment of Pharmacology, Wayne State University School of Medicine, Detroit, MI, USA.ORCID 0000-0003-2909-4779
Michael U CallaghanDivision of Pediatric Hematology and Oncology, Children's Hospital of Michigan, Detroit, MI, USA.
Xiufeng GaoFunctional Fluidics, Children's Hospital of Michigan, Detroit, MI, USA.
Ke LiuFunctional Fluidics, Children's Hospital of Michigan, Detroit, MI, USA.
Ahmar ZaidiDivision of Pediatric Hematology and Oncology, Children's Hospital of Michigan, Detroit, MI, USA.ORCID 0000-0003-4551-661X
Michael TarasevFunctional Fluidics, Children's Hospital of Michigan, Detroit, MI, USA.
Patrick C HinesFunctional Fluidics, Children's Hospital of Michigan, Detroit, MI, USA.
Children's Hospital of Michigan · USWayne State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sickle cell disease (SCD) is characterized by frequent and unpredictable vaso-occlusive crises (VOCs). Sickle erythrocytes (SSRBCs) contribute to VOCs by participating in a series of adhesive events with blood cells and the vascular endothelium. Adhesion assays have been used to evaluate the relationship between SSRBC adhesion and SCD severity. We developed a standardized, clinical flow adhesion assay of whole blood to vascular cell adhesion molecule (FA-WB-VCAM). The objective of this study was to assess the variability and clinical predictive value of FA-WB-VCAM in a six-month longitudinal, observational study (ELIPSIS) in SCD subjects during at-home, steady-state and self-reported VOCs, and following VOC resolution. We observed a strong relationship between FA-WB-VCAM and SCD severity. Adhesion indices were significantly lower in SCD subjects on hydroxycarbamide and increased during VOCs; at-home VOCs had significantly higher FA-WB-VCAM than steady-state and contact VOCs. SCD subjects with a high frequency of self-reported VOCs had a pro-adhesive phenotype at steady state and were stratified into a high-adhesive phenotype cohort; two years prospectively we observed a higher frequency of VOCs in the high-adhesion cohort. This study supports stratifying SCD subjects based on steady-state FA-WB-VCAM and suggests that FA-WB-VCAM may be a plausible surrogate end-point for SCD severity.

Indexed as

Anemia, Sickle CellCase-Control StudiesHumansLongitudinal StudiesVascular Cell Adhesion Molecule-1Vascular Cell Adhesion Molecule-1adhesionsickle cell diseasevascular cell adhesion molecule-1vaso-occlusionvery late antigen-4

Identifiers

PMID34850378
PMCPMC9299835
OpenAlexW3216048923

What OpenQuestion holds

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LicenceCC BY-NC
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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.