Evidence map›Paper›PMID 19054699›Full record

ArticleBlood cells, molecules & diseases

Fibrin architecture in clots: a quantitative polarized light microscopy analysis.

Peter Whittaker, Karin Przyklenk

Open access · greenAbstract readEvaluation Study
In one paragraph

Article in Blood cells, molecules & diseases. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

23 citing papers in PubMed, 54 citations in OpenAlex.

  1. Fibrin as a Versatile Fibrous Biopolymer.Sub-cellular biochemistry · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Fibrin Formation, Structure and Properties.Sub-cellular biochemistry · 2017
    Review
  9. Article
  10. Biophysical Mechanisms Mediating Fibrin Fiber Lysis.BioMed research international · 2017
    Review
  11. Article
  12. Article
  13. Efficacy of histotripsy combined with rt-PA in vitro.Physics in medicine and biology · 2016
    Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  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

2 authors at 1 institution in 1 country.

Peter WhittakerCardiovascular Research Institute, Department of Emergency Medicine, Wayne State University, School of Medicine, Detroit, MI 48201, USA. peter.whittaker@wayne.edu
Karin Przyklenk
Wayne State University · US

Funding

Preconditioning Improves Coronary PatencyR01HL072684 · NHLBI · WAYNE STATE UNIVERSITY · PI PRZYKLENK, KARIN · 2002 to 2012
$2.2M
Preconditioning Improves Coronary PatencyR56HL072684 · NHLBI · WAYNE STATE UNIVERSITY · PI PRZYKLENK, KARIN · 2007 to 2007
$394k
NHLBI NIH HHS R01 HL072684NHLBI NIH HHS R01 HL 72684NHLBI NIH HHS R56 HL072684NHLBI NIH HHS R56 HL72684
6 · The paper itself

Abstract

Fibrin plays a vital structural role in thrombus integrity. Thus, the ability to assess fibrin architecture has a potential to provide insight into thrombosis and thrombolysis. Fibrin has an anisotropic molecular structure, which enables it to be seen with polarized light. Therefore, we aimed to determine if automated polarized light microscopy methods of quantifying two structural parameters; fibrin fiber bundle orientation and fibrin's optical retardation (OR: a measure of molecular anisotropy) could be used to assess thrombi. To compare fibrin fiber bundle orientation we analyzed picrosirius red-stained sections obtained from clots formed: (A) in vitro, (B) in injured and stenotic coronary arteries, and (C) in surgically created aortic aneurysms (n=6 for each group). To assess potential changes in OR, we examined fibrin in picrosirius red-stained clots formed after ischemic preconditioning (10 min ischemia+10 min reflow; a circumstance shown to enhance lysability) and in control clots (n=8 each group). The degree of fibrin organization differed significantly according to the location of clot formation; fibrin was most aligned in the aneurysms and least aligned in vitro whereas fibrin in the coronary clots had an intermediate organization. The OR of fibrin in the clots formed after ischemic preconditioning was lower than that in controls (2.9+/-0.5 nm versus 5.4+/-1.0 nm, P<0.05). The automated polarized light analysis methods not only enabled fibrin architecture to be assessed, but also revealed structural differences in clots formed under different circumstances.

Indexed as

AnimalsBlood CoagulationColoring AgentsFibrinHumansMicroscopy, PolarizationThrombosisColoring AgentsFibrin

Identifiers

PMID19054699
PMCPMC2649791
OpenAlexW1993401250

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.