Evidence map›Paper›PMID 26001742›Full record

ArticleJournal of mathematical biology2016

Modelling of platelet-fibrin clot formation in flow with a DPD-PDE method.

A Tosenberger, F Ataullakhanov, N Bessonov, M Panteleev, A Tokarev, V Volpert

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PubMed Publisher
In one paragraph

Article in Journal of mathematical biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 20% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 5 citations in OpenAlex.

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  9. A model of fluid-structure and biochemical interactions for applications to subclinical leaflet thrombosis.International journal for numerical methods in biomedical engineering · 2023
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  19. Mathematical and Computational Modeling of Device-Induced Thrombosis.Current opinion in biomedical engineering · 2021
    Article
  20. Patient-Specific Modelling of Blood Coagulation.Bulletin of mathematical biology · 2021
    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

6 authors at 4 institutions in 2 countries.

A TosenbergerInstitut des Hautes Etudes Scientifiques, Bures-sur-Yvette, France. tosenberger@math.univ-lyon1.fr.
F AtaullakhanovFederal Research and Clinical Centre of Pediatric Hematology, Oncology and Immunology, Ministry of Healthcare of the Russian Federation, Moscow, Russian Federation.
N BessonovInstitute of Mechanical Engineering Problems, Saint Petersburg, Russian Federation.
M PanteleevFederal Research and Clinical Centre of Pediatric Hematology, Oncology and Immunology, Ministry of Healthcare of the Russian Federation, Moscow, Russian Federation.
A TokarevFederal Research and Clinical Centre of Pediatric Hematology, Oncology and Immunology, Ministry of Healthcare of the Russian Federation, Moscow, Russian Federation.
V VolpertInstitut Camille Jordan, UMR 5208 CNRS, University Lyon 1, Lyon, France.
Ministry of Health of the Russian Federation · RUCentre National de la Recherche Scientifique · FRInstitute of Problems of Mechanical Engineering · RUUniversité Claude Bernard Lyon 1 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The paper is devoted to mathematical modelling of clot growth in blood flow. Great complexity of the hemostatic system dictates the need of usage of the mathematical models to understand its functioning in the normal and especially in pathological situations. In this work we investigate the interaction of blood flow, platelet aggregation and plasma coagulation. We develop a hybrid DPD-PDE model where dissipative particle dynamics (DPD) is used to model plasma flow and platelets, while the regulatory network of plasma coagulation is described by a system of partial differential equations. Modelling results confirm the potency of the scenario of clot growth where at the first stage of clot formation platelets form an aggregate due to weak inter-platelet connections and then due to their activation. This enables the formation of the fibrin net in the centre of the platelet aggregate where the flow velocity is significantly reduced. The fibrin net reinforces the clot and allows its further growth. When the clot becomes sufficiently large, it stops growing due to the narrowed vessel and the increase of flow shear rate at the surface of the clot. Its outer part is detached by the flow revealing the inner part covered by fibrin. This fibrin cap does not allow new platelets to attach at the high shear rate, and the clot stops growing. Dependence of the final clot size on wall shear rate and on other parameters is studied.

Indexed as

Models, BiologicalAnimalsBlood CoagulationBlood PlateletsComputational BiologyFibrinHemorheologyHemostasisHumansMathematical ConceptsPlatelet AdhesivenessPlatelet AggregationFibrinBlood coagulationClot growthDissipative particle dynamicsHybrid models

Identifiers

PMID26001742
OpenAlexW1755633269

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.