Evidence map›Paper›PMID 32503419›Full record

ArticleBMC immunology2020

Can presepsin uniformly respond to various pathogens? - an in vitro assay of new sepsis marker.

Yusuke Koizumi, Daisuke Sakanashi, Tetsuo Mohri, Hiroki Watanabe, Arufumi Shiota, Nobuhiro Asai, Hideo Kato, Mao Hagihara, Kenta Murotani, Yuka Yamagishi and 2 more

Open access · goldAbstract read
In one paragraph

Article in BMC immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 19 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

12 authors at 3 institutions in 1 country.

Yusuke KoizumiDepartment of Clinical Infectious Diseases, Aichi Medical University Hospital, 1-1 Yazakokarimata, Nagakute, Aichi, 480-1195, Japan. ykoizumi@aichi-med-u.ac.jp.ORCID 0000-0001-9369-8767
Daisuke SakanashiDepartment of Infection Control, Aichi Medical University Hospital, Nagakute, Aichi, Japan.
Tetsuo MohriDepartment of Infection Control, Aichi Medical University Hospital, Nagakute, Aichi, Japan.
Hiroki WatanabeDepartment of Clinical Infectious Diseases, Aichi Medical University Hospital, 1-1 Yazakokarimata, Nagakute, Aichi, 480-1195, Japan.
Arufumi ShiotaDepartment of Infection Control, Aichi Medical University Hospital, Nagakute, Aichi, Japan.
Nobuhiro AsaiDepartment of Clinical Infectious Diseases, Aichi Medical University Hospital, 1-1 Yazakokarimata, Nagakute, Aichi, 480-1195, Japan.
Hideo KatoDepartment of Infection Control, Aichi Medical University Hospital, Nagakute, Aichi, Japan.
Mao HagiharaDepartment of Infection Control, Aichi Medical University Hospital, Nagakute, Aichi, Japan.
Kenta MurotaniBiostatistics center, Graduate School of Medicine, Kurume University, Kurume, Fukuoka, Japan.
Yuka YamagishiDepartment of Clinical Infectious Diseases, Aichi Medical University Hospital, 1-1 Yazakokarimata, Nagakute, Aichi, 480-1195, Japan.
Hiroyuki SuematsuDepartment of Infection Control, Aichi Medical University Hospital, Nagakute, Aichi, Japan.
Hiroshige MikamoDepartment of Clinical Infectious Diseases, Aichi Medical University Hospital, 1-1 Yazakokarimata, Nagakute, Aichi, 480-1195, Japan.
Aichi Medical University Hospital · JPAichi Medical University · JPKurume University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPresepsin (soluble CD14 subtype) is a novel biomarker of sepsis used for early diagnosis. Originally, CD14 is known as the pattern recognition receptor for the lipopolysaccharide (LPS)/LBP complexes, and the diagnostic value of this molecule for gram-positive bacteria, which contain less amount of LPS, is uncertain. To confirm its effectiveness in the diagnosis of bacteremia caused by gram positive bacteria, and to evaluate the interspecies difference of presepsin production against various bacterial strains, we conducted an in vitro assay to evaluate presepsin levels in response to five Gram negative and four Gram positive bacteria.

resultsWhole blood was yielded from five healthy volunteers and co-cultured with bacterial strains at 37 °C for 4 h. Twenty seven clinical isolates of nine species (E. coli, K. pneumoniae, E. cloacae, P. aeruginosa, S. maltophilia, S. aureus, S. pyogenes, B. cereus, and C. striatum) derived from blood cultures of non-neutropenic bacteremia patients were used. Culture supernatants were harvested and presepsin levels were measured. The presepsin level in the gram-negative bacteria 273 (218-352) pg/mL was significantly higher than in the gram-positive bacteria 200 (143-275) pg/mL (p = 0.0002). The presepsin levels were significantly lower in C. striatum, in comparison to other bacteria, and S. pyogenes showed similar results. And the presepsin levels in P. aeruginosa were significantly lower compared to E. cloacae, K. pneumoniae, and S. aureus.

conclusionsPresepsin production can also be evoked by gram-positive bacteria, and interspecies differences of presepsin response may exist, which should be considered in the diagnosis of sepsis, especially in certain gram-positive bacteremia such as S. pyogenes or C. striatum.

Indexed as

BacteremiaBacteriaBiomarkersCoculture TechniquesHumansLipopolysaccharide ReceptorsLipopolysaccharidesPeptide FragmentsSepsisBiomarkersLipopolysaccharide ReceptorsLipopolysaccharidesPeptide Fragmentspresepsin protein, humanBacteremiaCD14Gram-negative bacteriaGram-positive bacteriaIn vitro assayLipopolysaccharidePresepsin

Identifiers

PMID32503419
PMCPMC7275309
OpenAlexW3032943720

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Registered trials

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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.