Evidence map›Paper›PMID 22915644›Full record

ArticleBlood2012

Protective anti-inflammatory effect of ADAMTS13 on myocardial ischemia/reperfusion injury in mice.

Simon F De Meyer, Alexander S Savchenko, Michael S Haas, Daphne Schatzberg, Michael C Carroll, Alexandra Schiviz, Barbara Dietrich, Hanspeter Rottensteiner, Friedrich Scheiflinger, Denisa D Wagner

Open access · bronzeAbstract readEvaluation Study
In one paragraph

Article in Blood, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed, 1 pooled it
6.0field-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.

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

68 citing papers in PubMed, 1 synthesis or guideline pooled it, 117 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Arginine Methylation by PRMT1 Affects ADAMTS13 Secretion and Enzymatic Activity.Arteriosclerosis, thrombosis, and vascular biology · 2025
    Article
  8. Article
  9. The effect of ADAMTS13 on graft-versus-host disease.Journal of cellular and molecular medicine · 2024
    Article
  10. Thromboinflammation and the Role of Platelets.Arteriosclerosis, thrombosis, and vascular biology · 2024
    Article
  11. Review
  12. Article
  13. Article
  14. Mechanisms of ADAMTS13 regulation.Journal of thrombosis and haemostasis : JTH · 2022
    Review
  15. Review
  16. Altered VWF:ADAMTS13 homeostasis is a target for therapeutic intervention in sickle cell disease.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  17. Article
  18. Anti-inflammatory protective effect of ADAMTS-13 in murine arthritis models.Journal of thrombosis and haemostasis : JTH · 2022
    Article
  19. Thromboinflammation: From Atherosclerosis to COVID-19.Arteriosclerosis, thrombosis, and vascular biology · 2022
    Review
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 3 countries.

Simon F De MeyerImmune Disease Institute, Boston, MA 02115, USA.
Alexander S Savchenko
Michael S Haas
Daphne Schatzberg
Michael C Carroll
Alexandra Schiviz
Barbara Dietrich
Hanspeter Rottensteiner
Friedrich Scheiflinger
Denisa D Wagner
Baxter (Austria) · ATBoston Biomedical Research Institute · USBoston Children's Hospital · USDecImmune Therapeutics (United States) · USHarvard University · US

Funding

WEIBEL-PALADE BODY FORMATION AND ROLE IN HEMOSTASISR01HL041002 · NHLBI · TUFTS MEDICAL CENTER · PI WAGNER, DENISA D · 1988 to 2013
$2.0M
NHLBI NIH HHS R01 HL041002
6 · The paper itself

Abstract

Coronary heart disease is a major cause of death in the western world. Although essential for successful recovery, reperfusion of ischemic myocardium is inevitably associated with reperfusion injury. To investigate a potential protective role of ADAMTS13, a protease cleaving von Willebrand factor multimers, during myocardial ischemia/reperfusion, we used a mouse model of acute myocardial infarction. We found that Adamts13(-/-) mice developed larger myocardial infarctions than wild-type control mice, whereas treatment of wild-type mice with recombinant human ADAMTS13 (rhADAMTS13) led to smaller infarctions. The protective effect of ADAMTS13 was further confirmed by a significant reduction of cardiac troponin-I release and less myocardial apoptosis in mice that received rhADAMTS13 compared with controls. Platelets adherent to the blood vessel wall were observed in few areas in the heart samples from mice treated with vehicle and were not detected in samples from mice treated with rhADAMTS13. However, we observed a 9-fold reduction in number of neutrophils infiltrating ischemic myocardium in mice that were treated with rhADAMTS13, suggesting a potent anti-inflammatory effect of ADAMTS13 during heart injury. Our data show that ADAMTS13 reduces myocardial ischemia/reperfusion injury in mice and indicate that rhADAMTS13 could be of therapeutic value to limit myocardial ischemia/reperfusion injury.

Indexed as

ADAM ProteinsADAMTS13 ProteinAnimalsAnti-Inflammatory AgentsCardiotonic AgentsCHO CellsCricetinaeCricetulusCytoprotectionHumansMaleMetalloendopeptidasesMiceMice, Inbred C57BLMice, KnockoutMyocardial Reperfusion InjuryADAM ProteinsADAMTS13 ProteinADAMTS13 protein, humanADAMTS13 protein, mouseAnti-Inflammatory AgentsCardiotonic AgentsMetalloendopeptidasesRecombinant Proteins

Identifiers

PMID22915644
PMCPMC3537313
OpenAlexW2103323679

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.