Evidence map›Paper›PMID 23590132›Full record

ArticleBritish journal of haematology2013

Paradoxical protection from atherosclerosis and thrombosis in a mouse model of sickle cell disease.

Hui Wang, Wei Luo, Jintao Wang, Chiao Guo, Stephanie L Wolffe, Julia Wang, Eddy B Sun, Kori N Bradley, Andrew D Campbell, Daniel T Eitzman

Open access · greenAbstract read
In one paragraph

Article in British journal of haematology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

13 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Accelerated atherosclerosis in beta-thalassemia.American journal of physiology. Heart and circulatory physiology · 2023
    Article
  5. Article
  6. Sickle Cell Disease: A Paradigm for Venous Thrombosis Pathophysiology.International journal of molecular sciences · 2020
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. 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

10 authors at 2 institutions in 1 country.

Hui WangDepartment of Internal Medicine, Cardiovascular Research Center, University of Michigan, Ann Arbor, MI, USA.
Wei Luo
Jintao Wang
Chiao Guo
Stephanie L Wolffe
Julia Wang
Eddy B Sun
Kori N Bradley
Andrew D Campbell
Daniel T Eitzman
University of Michigan–Ann Arbor · USMichigan Medicine · US

Funding

Leptin in Vascular DiseaseR01HL073150 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI EITZMAN, DANIEL T · 2003 to 2012
$3.3M
NETs in the development of lupus and its cardiovascular complicationsR01HL088419 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI EITZMAN, DANIEL T · 2009 to 2016
$3.1M
Regulation of Adipose Tissue Inflammation by P-selectin Glycoprotein Ligand-1I01BX000353 · VA · VETERANS HEALTH ADMINISTRATION · PI EITZMAN, DANIEL T · 2009 to 2013
–
BLRD VA I01 BX000353NHLBI NIH HHS HL073150NHLBI NIH HHS R01 HL073150NHLBI NIH HHS R01 HL088419
6 · The paper itself

Abstract

Sickle cell disease (SCD) is associated with vascular complications including premature stroke. The role of atherothrombosis in these vascular complications is unclear. To determine the effect of SCD on atherosclerosis and thrombosis, mice with SCD along with controls were generated by transplantation of bone marrow from mice carrying the homozygous sickle cell mutation (Hbb(hβs/hβs) ) or wild-type mice (Hbb(+/+) ) into C57BL6/J or apolipoprotein E deficient (Apoe(-/-) ) recipient mice. At the time of sacrifice, 23-28 weeks following bone marrow transplantation, anaemia, reticulocytosis, and splenomegaly were present in mice receiving Hbb(hβs/hβs) bone marrow compared with control mice. Analysis of atherosclerosis involving the aortic root revealed reduced atherosclerotic lesion area with reduced macrophage content and increased collagen content in Apoe(-/-) , Hbb(hβs/hβs) mice compared to Apoe(-/-) , Hbb(+/+) mice. In a carotid thrombosis model, the time to thrombosis was prolonged in Hbb(hβs/hβs) mice compared to Hbb(+/+) mice. This apparent protective effect of SCD on atherosclerosis and thrombosis was diminished by inhibition of heme oxygenase-1 (HMOX1) using zinc protoporphyrin IX. We conclude that SCD in mice is paradoxically protective against atherosclerosis and thrombosis, highlighting the complexity of vascular events in SCD. This protective effect is at least partially mediated by induction of HMOX1.

Indexed as

Anemia, Sickle CellAnimalsAortaApolipoproteins EAtherosclerosisCarotid ArteriesDisease Models, AnimalHeme Oxygenase-1LipidsMaleMiceMice, KnockoutProtoporphyrinsThrombosisApolipoproteins EHeme Oxygenase-1LipidsProtoporphyrinszinc protoporphyrin

Identifiers

PMID23590132
PMCPMC4780334
OpenAlexW2059495092

What OpenQuestion holds

Textmetadata
LicenceTDM
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.