Evidence map›Paper›PMID 30638104›Full record

ArticleThe International journal of artificial organs2019

A new hydrophilic polysulfone hemodialysis membrane can prevent platelet-neutrophil interactions and successive neutrophil activation.

Yoko Koga, Hiroyuki Meguro, Hiroaki Fujieda, Yoshiyuki Ueno, Keishi Miwa, Mie Kainoh

Open access · bronzeAbstract read
In one paragraph

Article in The International journal of artificial organs, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

10 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
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  9. In vitro blood compatibility evaluation method: incubating while rotating hemodialyzers filled with fresh human blood.Journal of artificial organs : the official journal of the Japanese Society for Artificial Organs · 2021
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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

6 authors at 1 institution in 1 country.

Yoko Koga1 Pharmaceutical Research Laboratories, Toray Industries, Inc., Kamakura, Japan.
Hiroyuki Meguro1 Pharmaceutical Research Laboratories, Toray Industries, Inc., Kamakura, Japan.
Hiroaki Fujieda2 Advanced Material Research Laboratories, Toray Industries, Inc., Otsu, Japan.
Yoshiyuki Ueno2 Advanced Material Research Laboratories, Toray Industries, Inc., Otsu, Japan.
Keishi Miwa2 Advanced Material Research Laboratories, Toray Industries, Inc., Otsu, Japan.
Mie Kainoh1 Pharmaceutical Research Laboratories, Toray Industries, Inc., Kamakura, Japan.
Toray Industries, Inc. (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose: Microaggregates have often been observed during hemodialysis and are clearly associated with complications of hemodialysis therapy. In this study, we aimed to clarify the effects of two polysulfone membranes, with different abilities to activate blood cells, on the formation of these microaggregates; we also investigated their molecular mechanisms.

methods: Human whole blood was circulated through a mini-module dialyzer using the membranes in vitro; platelet-neutrophil complexes in blood were determined by flow cytometry. Isolated human neutrophils were incubated with the membranes in plasma, in the presence or absence of platelets, followed by flow cytometric analysis of intracellular reactive oxygen species and cell-surface activated CD11b on neutrophils.

results: CX-U, a conventional polysulfone membrane with remarkable cell activation, induced the formation of platelet-neutrophil complexes; however, NV-U, a new hydrophilic polysulfone membrane with slight or no cell activation, did not cause complex formation. Moreover, CX-U-induced reactive oxygen species production and the increase in activated CD11b expression on neutrophils were enhanced by platelets. On the other hand, NV-U hardly affected neutrophil activation, regardless of whether platelets were present or not. The enhancement of CX-U-induced neutrophil activations by platelets was greatly inhibited by anti-CD62P antibody.

conclusion: The ability of polysulfone membranes to activate blood cells is closely related to platelet-neutrophil interaction. Therefore, a biocompatible membrane, like NV-U, can be expected to prevent microaggregate formation during hemodialysis and avoid subsequent cell activation.

Indexed as

Membranes, ArtificialRenal DialysisBiocompatible MaterialsBlood PlateletsCD11b AntigenCell CommunicationFlow CytometryHumansNeutrophil ActivationNeutrophilsPlatelet ActivationPolymersP-SelectinReactive Oxygen SpeciesSulfonesSurface PropertiesBiocompatible MaterialsCD11b AntigenITGAM protein, humanMembranes, ArtificialPolymerspolysulfone P 1700P-SelectinReactive Oxygen SpeciesSELP protein, humanSulfonesadhesion moleculesapheresis and detoxification techniquesartificial kidneyblood compatibilitycharacterization of biomaterial surface propertiesHemodialysisplatelet–material interactions

Identifiers

PMID30638104
PMCPMC6421590
OpenAlexW2910181981

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LicenceCC BY-NC
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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.