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Predictive value of serum gelsolin and Gc globulin in sepsis – a pilot study

  • Zoltán Horváth-Szalai , Péter Kustán , Balázs Szirmay , Ágnes Lakatos , Per Hjort Christensen , Tamás Huber , Beáta Bugyi , Diána Mühl , Andrea Ludány , Attila Miseta , Gábor L. Kovács and Tamás Kőszegi EMAIL logo
Published/Copyright: January 10, 2018

Abstract

Background:

Simultaneous determination of the two main actin scavenger proteins in sepsis has not been investigated until now. In our pilot study, we elucidated the predictive values of Gc globulin and gelsolin (GSN) in sepsis by comparing them to classic laboratory and clinical parameters.

Methods:

A 5-day follow-up was performed, including 46 septic patients, 28 non-septic patients and 35 outpatients as controls. Serum Gc globulin and GSN levels were determined by automated immune turbidimetric assay on a Cobas 8000/c502 analyzer. Patients were retrospectively categorized according to the sepsis-3 definitions, and 14-day mortality was also investigated.

Results:

First-day GSN also differentiated sepsis from non-sepsis (AUC: 0.88) similarly to C-reactive protein (AUC: 0.80) but was slightly inferior to procalcitonin (PCT) (AUC: 0.98) with a cutoff value of GSN at 22.29 mg/L (sensitivity: 83.3%; specificity: 86.2%). Only first-day SOFA scores (0.88) and GSN (0.71) distinguished septic survivors from non-survivors, whereas lactate (0.99), Gc globulin (0.76) and mean arterial pressure (MAP) (0.74) discriminated septic shock from sepsis. Logistic regression analyses revealed SOFA scores and GSN being significant factors regarding 14-day mortality. First-day GSN levels were higher (p<0.05) in septic survivors than in non-survivors. Gc globulin levels remained higher (p<0.01) in sepsis when compared with septic shock during the follow-up period.

Conclusions:

Both serum GSN and Gc globulin may have predictive values in sepsis. Considering the small sample size of our study, further measurements are needed to evaluate our results. Measurement of Gc globulin and GSN maybe useful in assessment of sepsis severity and in therapeutic decision-making.


Corresponding author: Prof. Dr. Tamás Kőszegi, Department of Laboratory Medicine, University of Pécs, Medical School, Ifjúság u. 13, 7624 Pécs, Hungary, Phone: +36 30 491 7719, Fax: +36 72 536 121, E-mail:

Acknowledgments

The present scientific contribution is dedicated to the 650th anniversary of the foundation of the University of Pécs, Hungary. We are grateful to Agilent Technologies for providing us the GSN reagents.

  1. Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Research funding: This research was partly supported by GINOP-2.3.2-15-2016-00021 “The use of chip-technology in increasing the effectiveness of human in vitro fertilization” and NKFI-EPR K/115394/2015 “Early biochemical indicators of embryo viability”, and KA-2016-04 grants. Our work was also supported by the Hungarian Science Foundation (OTKA) grant nos. K109689 and 115394 by the European Union and the State of Hungary, co-financed by the European Social Fund in the framework of TÁMOP 4.2.4.A/2-11-1-2012-0001 “National Excellence Program” and the New National Excellence Program of the Ministry of Human Capacities. Also supported by the ÚNKP-16-4 and the by the ÚNKP-17-3-III New National Excellence Program of the Ministry of Human Capacities.

  3. Employment or leadership: None declared.

  4. Honorarium: None declared.

  5. Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

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Received: 2017-08-31
Accepted: 2017-11-09
Published Online: 2018-01-10
Published in Print: 2018-07-26

©2018 Walter de Gruyter GmbH, Berlin/Boston

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