Evidence map›Paper›PMID 21304105›Full record

ArticleBlood2011

Mechanisms of enhanced thrombus formation in cerebral microvessels of mice expressing hemoglobin-S.

Felicity N E Gavins, Janice Russell, Elena L Senchenkova, Lidiana De Almeida Paula, Amílcar S Damazo, Charles T Esmon, Daniel Kirchhofer, Robert P Hebbel, D Neil Granger

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

36 citing papers in PubMed, 58 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Regulating Neutrophil PAD4/NOX-Dependent Cerebrovasular Thromboinflammation.International journal of biological sciences · 2023
    Article
  10. Cardiac pathophysiology in sickle cell disease.Journal of thrombosis and thrombolysis · 2021
    Review
  11. Article
  12. Article
  13. Article
  14. Sickle Cell Disease: A Paradigm for Venous Thrombosis Pathophysiology.International journal of molecular sciences · 2020
    Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. 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

9 authors at 5 institutions in 3 countries.

Felicity N E GavinsWolfson Neuroscience Laboratories, Faculty of Medicine, Imperial College, London, UK. f.gavins@imperial.ac.uk
Janice Russell
Elena L Senchenkova
Lidiana De Almeida Paula
Amílcar S Damazo
Charles T Esmon
Daniel Kirchhofer
Robert P Hebbel
D Neil Granger
Louisiana State University Health Sciences Center Shreveport · USImperial College London · GBOklahoma Medical Research Foundation · USUniversidade Federal de Mato Grosso · BRUniversity of Minnesota Medical Center · US

Funding

VASCULAR PATHOBIOLOGY OF SICKLE CELL DISEASEP01HL055552 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI HEBBEL, ROBERT P · 1995 to 2011
$17.3M
TRANSCAPILLARY FLUID EXCHANGER01HL026441 · NHLBI · UNIVERSITY OF SOUTH ALABAMA · PI GRANGER, D. NEIL · 1985 to 2013
$4.0M
Validation of extracellular histones as biomarker and therapeutic target in sepsiRC1GM091739 · NIGMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI ESMON, CHARLES T, KINASEWITZ, GARY · 2009 to 2010
$1.0M
Biotechnology and Biological Sciences Research Council BB/E52708X/1NHLBI NIH HHS HL26441NHLBI NIH HHS P01 HL055552NHLBI NIH HHS P01-HL55552NHLBI NIH HHS R01 HL026441NIGMS NIH HHS GM091739NIGMS NIH HHS RC1 GM091739
6 · The paper itself

Abstract

The microvasculature assumes an inflammatory and procoagulant state in a variety of different diseases, including sickle cell disease (SCD), which may contribute to the high incidence of ischemic stroke in these patients. This study provides evidence for accelerated thrombus formation in arterioles and venules in the cerebral vasculature of mice that express hemoglobin-S (β(s) mice). Enhanced microvascular thrombosis in β(s) mice was blunted by immunologic or genetic interventions that target tissue factor, endothelial protein C receptor, activated protein C, or thrombin. Platelets from β(s) mice also exhibited enhanced aggregation velocity after stimulation with thrombin but not ADP. Neutropenia also protected against the enhanced thrombosis response in β(s) mice. These results indicate that the cerebral microvasculature is rendered vulnerable to thrombus formation in β(s) mice via a neutrophil-dependent mechanism that is associated with an increased formation of and enhanced platelet sensitivity to thrombin.

Indexed as

Anemia, Sickle CellIntracranial ThrombosisAnimalsBlood PlateletsBone Marrow TransplantationCerebral ArteriesDisease Models, AnimalHemoglobin, SickleMaleMiceMice, 129 StrainMice, Inbred C57BLMice, Inbred DBAMice, Mutant StrainsMicrocirculationNeutrophilsHemoglobin, SickleProtein CThrombinThromboplastin

Identifiers

PMID21304105
PMCPMC3087535
OpenAlexW2039453307

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.