Evidence map›Paper›PMID 30239013›Full record

ArticleArtificial organs2018

Biocompatibility of Polysulfone Hemodialysis Membranes and Its Mechanisms: Involvement of Fibrinogen and Its Integrin Receptors in Activation of Platelets and Neutrophils.

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

Open access · hybridAbstract read
In one paragraph

Article in Artificial organs, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
6.4field-weighted citation impact, top 3% 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

37 citing papers in PubMed, 85 citations in OpenAlex.

  1. Trial
  2. Correlation between real sieving coefficient determined using novel lab-scale module and pore structure of hemodiafiltration membranes.Journal of artificial organs : the official journal of the Japanese Society for Artificial Organs · 2026
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  7. In Vitro Thrombogenicity Evaluation of Hemodialyzers.International journal of molecular sciences · 2026
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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

7 authors at 1 institution in 2 countries.

Yoko KogaDepartment of Pharmacology Laboratory, Pharmaceutical Research Laboratories, Toray Industries, Inc., Kamakura, Kanagawa.ORCID http://orcid.org/0000-0002-0908-7718
Hiroaki FujiedaDepartment of Medical Devices and Materials Research Laboratory, Advanced Material Research Laboratories, Toray Industries, Inc., Otsu, Siga, Japan.
Hiroyuki MeguroDepartment of Pharmacology Laboratory, Pharmaceutical Research Laboratories, Toray Industries, Inc., Kamakura, Kanagawa.
Yoshiyuki UenoDepartment of Medical Devices and Materials Research Laboratory, Advanced Material Research Laboratories, Toray Industries, Inc., Otsu, Siga, Japan.
Takao AokiDepartment of Medical Devices and Materials Research Laboratory, Advanced Material Research Laboratories, Toray Industries, Inc., Otsu, Siga, Japan.
Keishi MiwaDepartment of Medical Devices and Materials Research Laboratory, Advanced Material Research Laboratories, Toray Industries, Inc., Otsu, Siga, Japan.
Mie KainohDepartment of Pharmacology Laboratory, Pharmaceutical Research Laboratories, Toray Industries, Inc., Kamakura, Kanagawa.
Toray (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Activation of blood cells during hemodialysis is considered to be a significant determinant of biocompatibility of the hemodialysis membrane because it may affect patient health adversely through microvascular inflammation and oxidative stress. This study found very different cell activation among various polysulfone (PSf) hemodialysis membranes. For example, CX-U, a conventional PSf membrane, induced marked adhesion of platelets to its surface and increased surface expression of activated CD11b and production of reactive oxygen species (ROS) by neutrophils; while NV-U, a hydrophilic polymer-immobilized PSf membrane, caused little platelet adhesion and slight CD11b expression and ROS production by neutrophils. Analysis of the molecular mechanisms of the above phenomena on CX-U and NV-U indicated that anti-integrin GPIIb/IIIa antibody blocked platelet adhesion, and that the combination of anti-CD11b (integrin α subunit of Mac-1) and anti-integrin αvβ3 antibodies blocked ROS production by neutrophils. Plasma-derived fibrinogen, a major ligand of GPIIb/IIIa, Mac-1, and αvβ3 on membranes, was thus analyzed and found to be more adsorbed to CX-U than to NV-U. Moreover, comparison between five PSf membranes showed that the number of adherent platelets and neutrophil ROS production increased with increasing fibrinogen adsorption. These results suggested that fibrinogen, adsorbed on membranes, induced GPIIb/IIIa-mediated platelet activation and Mac-1/αvβ3-mediated neutrophil activation, depending on the amount of adsorption. In conclusion, the use of biocompatible membranes like NV-U, which show lower adsorption of fibrinogen, is expected to reduce hemodialysis-induced inflammation and oxidative stress by minimizing cell activation.

Indexed as

Biocompatible MaterialsMembranes, ArtificialPolymersSulfonesBlood PlateletsFibrinogenHumansNeutrophil ActivationNeutrophilsOxidative StressPlatelet ActivationPlatelet AdhesivenessReactive Oxygen SpeciesBiocompatible MaterialsFibrinogenMembranes, ArtificialPolymerspolysulfone P 1700Reactive Oxygen SpeciesSulfonesBiocompatibilityFibrinogenHemodialysis membraneNeutrophilPlatelet

Identifiers

PMID30239013
PMCPMC6220809
OpenAlexW2890712628

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.