Evidence map›Paper›PMID 28507082›Full record

Trial reportBlood2017

Association between diffuse myocardial fibrosis and diastolic dysfunction in sickle cell anemia.

Omar Niss, Robert Fleck, Fowe Makue, Tarek Alsaied, Payal Desai, Jeffrey A Towbin, Punam Malik, Michael D Taylor, Charles T Quinn

2 registry-linked trialsOpen access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Blood, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 65 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed, 1 pooled it
6.8field-weighted citation impact, top 3% 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.

NCT02410811 completednot on this map

Novel Cardiac Magnetic Resonance Imaging to Define a Unique Restrictive Cardiomyopathy in Sickle Cell Disease

TypeobservationalSponsorChildren's Hospital Medical Center, CincinnatiRan2014 to 2019Enrolled33ConditionsSickle Cell DiseaseArmsCardiac magnetic resonance imaging (CMR)
NCT05469828 phase1 / phase2not yet recruitingnot on this mapstarted 2024, after this paper: background citation

Crizanlizumab Improves Tissue Oxygen Supply Demand Matching in Patients With Sickle Cell Anemia

TypeinterventionalSponsorChildren's Hospital Los AngelesRan2024 to 2029Enrolled30ConditionsSickle Cell DiseaseArmsCrizanlizumab, control
3 · Its place in the literature

Who cites it

65 citing papers in PubMed, 1 synthesis or guideline pooled it, 111 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

5 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Omar NissDivision of Hematology.
Robert FleckDepartment of Radiology, and.
Fowe MakueDivision of Cardiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Tarek AlsaiedDivision of Cardiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Payal DesaiDepartment of Internal Medicine, The Ohio State University, Columbus, OH.
Jeffrey A TowbinThe Heart Institute, Le Bonheur Children's Hospital, Memphis, TN; and.
Punam MalikDivision of Hematology.
Michael D TaylorDivision of Cardiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Charles T QuinnDivision of Hematology.
Cincinnati Children's Hospital Medical Center · USLe Bonheur Children's Hospital · USThe Ohio State University · US

Funding

Cincinnati Center of Excellence in Hemoglobinopathies ResearchU01HL117709 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI MALIK, PUNAM · 2013 to 2017
$8.9M
NHLBI NIH HHS U01 HL117709
6 · The paper itself

Abstract

Sickle cell anemia (SCA)-related cardiomyopathy is characterized by diastolic dysfunction and hyperdynamic features. Diastolic dysfunction portends early mortality in SCA. Diastolic dysfunction is associated with microscopic myocardial fibrosis in SCA mice, but the cause of diastolic dysfunction in humans with SCA is unknown. We used cardiac magnetic resonance measurements of extracellular volume fraction (ECV) to discover and quantify diffuse myocardial fibrosis in 25 individuals with SCA (mean age, 23 ± 13 years) and determine the association between diffuse myocardial fibrosis and diastolic dysfunction. ECV was calculated from pre- and post-gadolinium T1 measurements of blood and myocardium, and diastolic function was assessed by echocardiography. ECV was markedly increased in all participants compared with controls (0.44 ± 0.08 vs 0.26 ± 0.02,

Indexed as

DiastoleAdolescentAdultAnemia, Sickle CellBiomarkersCardiomyopathiesChildEchocardiographyEndomyocardial FibrosisFemaleGene ExpressionHemoglobinsHumansLongitudinal StudiesMagnetic Resonance ImagingMaleBiomarkersHemoglobinsNatriuretic Peptide, BrainPeptide Fragmentspro-brain natriuretic peptide (1-76)

Identifiers

PMID28507082
PMCPMC5510791
OpenAlexW2614195538

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.