Evidence map›Paper›PMID 28872708›Full record

ArticleJournal of clinical laboratory analysis2018

Validation of an automated immune turbidimetric assay for serum gelsolin and its possible clinical utility in sepsis.

Zoltán Horváth-Szalai, Péter Kustán, Balázs Szirmay, Ágnes Lakatos, Per H Christensen, Tamás Huber, Beáta Bugyi, Diána Mühl, Andrea Ludány, Attila Miseta and 2 more

Open access · bronzeAbstract read
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Article in Journal of clinical laboratory analysis, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 31% 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

6 citing papers in PubMed, 9 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 2 institutions in 2 countries.

Zoltán Horváth-SzalaiDepartment of Laboratory Medicine, University of Pécs, Pécs, Hungary.
Péter KustánDepartment of Laboratory Medicine, University of Pécs, Pécs, Hungary.
Balázs SzirmayDepartment of Laboratory Medicine, University of Pécs, Pécs, Hungary.
Ágnes LakatosDepartment of Laboratory Medicine, University of Pécs, Pécs, Hungary.
Per H ChristensenAgilent Technologies Denmark Aps, Glostrup, Denmark.
Tamás HuberDepartment of Biophysics, University of Pécs, Pécs, Hungary.
Beáta BugyiDepartment of Biophysics, University of Pécs, Pécs, Hungary.
Diána MühlDepartment of Anaesthesiology and Intensive Therapy, University of Pécs, Pécs, Hungary.
Andrea LudányDepartment of Laboratory Medicine, University of Pécs, Pécs, Hungary.
Attila MisetaDepartment of Laboratory Medicine, University of Pécs, Pécs, Hungary.
Gábor L KovácsDepartment of Laboratory Medicine, University of Pécs, Pécs, Hungary.
Tamás KőszegiDepartment of Laboratory Medicine, University of Pécs, Pécs, Hungary.ORCID http://orcid.org/0000-0002-3910-5745
University of Pecs · HUAgilent Technologies (Denmark) · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundStudies showing the potential predictive value of the actin-binding protein gelsolin, in critically ill patients are scarce. Moreover, even up to now a rapid automated measurement of gelsolin has still remained a challenge. Therefore, we developed and validated an automated serum gelsolin immune turbidimetric assay for possible clinical use.

methodsValidation of serum gelsolin assay was performed on a Cobas 8000/c502 analyzer (Roche) according to the second edition of Eurachem guidelines. Furthermore, we also studied the diagnostic value of serum gelsolin in sepsis when investigating sera of septic (n = 25), systemic inflammatory response syndrome (SIRS; n = 8) and control patients (n = 14). We compared our previously published Western blot data with those of the new turbidimetric assay.

resultsThe sample volume was 7 μL and the assay time was 10 minutes. The detection limit was 0.72 mg/L, intra- and inter-assay imprecision remained in most cases less than 5% expressed as CV. Recovery was found to be 84.56%-93.52% and linearity study gave an appropriate correlation coefficient by linear regression analysis (r

conclusionBased on the results, our immune turbidimetric measurement offers a rapid and accurate quantitation of gelsolin in human serum samples. Serum gelsolin seems a promising additional diagnostic marker of sepsis which has to be further investigated.

Indexed as

AdultAgedAged, 80 and overAutomation, LaboratoryFemaleGelsolinHumansLimit of DetectionLinear ModelsMaleMiddle AgedNephelometry and TurbidimetryReproducibility of ResultsROC CurveSepsisGelsolinautomationdiagnostic markerimmune turbidimetrysepsisserum gelsolin

Identifiers

PMID28872708
PMCPMC6817119
OpenAlexW2750754579

What OpenQuestion holds

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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.