Evidence map›Paper›PMID 38435796›Full record

ArticleCellular and molecular bioengineering2024

Influence of Hematocrit Level and Integrin α

Connor T Watson, Shane C Ward, Stefano A Rizzo, Alberto Redaelli, Keefe B Manning

Open access · greenAbstract read
In one paragraph

Article in Cellular and molecular bioengineering, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
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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

5 authors at 2 institutions in 2 countries.

Connor T WatsonDepartment of Biomedical Engineering, The Pennsylvania State University, University Park, PA USA.
Shane C WardDepartment of Biomedical Engineering, The Pennsylvania State University, University Park, PA USA.
Stefano A RizzoDepartment of Electronics, Information and Bioengineering, Politecnico di Milano, Milano, Italy.
Alberto RedaelliDepartment of Electronics, Information and Bioengineering, Politecnico di Milano, Milano, Italy.
Keefe B ManningDepartment of Biomedical Engineering, The Pennsylvania State University, University Park, PA USA.ORCID 0000-0001-9029-5217
Pennsylvania State University · USPolitecnico di Milano · IT

Funding

Penn State Clinical and Translational Science InstituteUL1TR002014 · NCATS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI KRASCHNEWSKI, JENNIFER L. · 2016 to 2025
$33.7M
A Structured Approach to the Design of Minimally Traumatic Blood PumpsR01HL136369 · NHLBI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI CYSYK, JOSHUA P, MANNING, KEEFE B · 2018 to 2021
$2.6M
NCATS NIH HHS UL1 TR002014NHLBI NIH HHS R01 HL136369
6 · The paper itself

Abstract

Purpose: Shear-mediated thrombosis is a clinically relevant phenomenon that underlies excessive arterial thrombosis and device-induced thrombosis. Red blood cells are known to mechanically contribute to physiological hemostasis through margination of platelets and vWF, facilitating the unfurling of vWF multimers, and increasing the fraction of thrombus-contacting platelets. Shear also plays a role in this phenomenon, increasing both the degree of margination and the near-wall forces experienced by vWF and platelets leading to unfurling and activation. Despite this, the contribution of red blood cells in shear-induced platelet aggregation has not been fully investigated-specifically the effect of elevated hematocrit has not yet been demonstrated. Methods: Here, a microfluidic model of a sudden expansion is presented as a platform for investigating platelet adhesion at hematocrits ranging from 0 to 60% and shear rates ranging from 1000 to 10,000 s Results: Increasing shear rates at physiological and elevated hematocrit levels facilitate robust platelet adhesion and formation of large aggregates. Shear-induced platelet aggregation is demonstrated to be dependent on both α Conclusions: This study highlights driving factors in vWF-mediated platelet adhesion that are relevant to clinical suppression of shear-induced thrombosis and in vitro assays of platelet adhesion. Primarily, increasing hematocrit promotes platelet margination, permitting shear-induced platelet aggregation through α Supplementary Information: The online version contains supplementary material available at 10.1007/s12195-024-00796-0.

Indexed as

MarginationPlateletsShearThrombosisvon Willebrand factor

Identifiers

PMID38435796
PMCPMC10902252
OpenAlexW4391878635

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.