Evidence map›Paper›PMID 36396711›Full record

ArticleScientific reports2022

Relationship between red blood cell aggregation and dextran molecular mass.

Maciej Bosek, Blanka Ziomkowska, Jerzy Pyskir, Tomasz Wybranowski, Małgorzata Pyskir, Michał Cyrankiewicz, Marta Napiórkowska, Maciej Durmowicz, Stefan Kruszewski

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

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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

9 authors at 1 institution in 1 country.

Maciej BosekBiophysics Department, Collegium Medicum of Nicolaus Copernicus University, Jagiellońska St. 13, 85-067, Bydgoszcz, Poland.
Blanka ZiomkowskaBiophysics Department, Collegium Medicum of Nicolaus Copernicus University, Jagiellońska St. 13, 85-067, Bydgoszcz, Poland.
Jerzy PyskirBiophysics Department, Collegium Medicum of Nicolaus Copernicus University, Jagiellońska St. 13, 85-067, Bydgoszcz, Poland. jerzy_pyskir@cm.umk.pl.
Tomasz WybranowskiBiophysics Department, Collegium Medicum of Nicolaus Copernicus University, Jagiellońska St. 13, 85-067, Bydgoszcz, Poland.
Małgorzata PyskirDepartment of Rehabilitation, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University, Toruń, Poland.
Michał CyrankiewiczBiophysics Department, Collegium Medicum of Nicolaus Copernicus University, Jagiellońska St. 13, 85-067, Bydgoszcz, Poland.
Marta NapiórkowskaBiophysics Department, Collegium Medicum of Nicolaus Copernicus University, Jagiellońska St. 13, 85-067, Bydgoszcz, Poland.
Maciej DurmowiczDepartment of Physiotherapy, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University, Toruń, Poland.
Stefan KruszewskiBiophysics Department, Collegium Medicum of Nicolaus Copernicus University, Jagiellońska St. 13, 85-067, Bydgoszcz, Poland.
Nicolaus Copernicus University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to investigate the aggregation of red blood cells (RBCs) suspended in dextran solution at various levels of molecular mass. Dextran solutions at molecular mass 40, 70, 100 and 500 kDa at concentration from 2 to 5 g/dL were used to suspend the RBCs. The radius and velocity of sedimenting RBC aggregates were investigated using image analysis. The radius and sedimentation velocity of aggregates increased initially, then decreased after achieving maxima. The maximal velocity of RBC aggregates showed a bell-shaped dependence on dextran molecular mass and concentration, whereas maximal radius showed monotonic increase with both factors. Difference between aggregate and solution density was estimated using aggregate radius and sedimentation velocity and dextran solution viscosity, and was consistent across most molecular mass and concentration levels. This allowed to calculate the porosity of aggregates and to show that it monotonically decreased with the increase in the solution density, caused by the increase in the dextran concentration. The results provide insight into the RBC aggregation process in solutions of proteins of different size, reflecting various pathological conditions. The currently reported data can be potentially applied to specific pathophysiological conditions giving an interpretation that is not yet fully discussed in the literature.

Indexed as

DextransErythrocyte AggregationErythrocyte CountErythrocytesMolecular WeightDextrans

Identifiers

PMID36396711
PMCPMC9670059
OpenAlexW4309475465

What OpenQuestion holds

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LicenceCC BY
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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.