Evidence map›Paper›PMID 26648775›Full record

ArticleCentral-European journal of immunology2015

Innate immunity gene expression changes in critically ill patients with sepsis and disease-related malnutrition.

Robert Słotwiński, Agnieszka Sarnecka, Aleksandra Dąbrowska, Katarzyna Kosałka, Ewelina Wachowska, Barbara J Bałan, Marta Jankowska, Teresa Korta, Grzegorz Niewiński, Andrzej Kański and 4 more

Open access · goldAbstract read
In one paragraph

Article in Central-European journal of immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

9 citing papers in PubMed, 20 citations in OpenAlex.

  1. Deciphering the Inflammatory Network in Pediatric Recurrent Tonsillitis: The Role of TRAF6, IRAK1, and miR-146a-5p.Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery · 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

14 authors at 3 institutions in 1 country.

Robert SłotwińskiDepartment of Surgical Research and Transplantology, Mossakowski Medical Research Center, Polish Academy of Sciences, Warsaw, Poland ; Department of Immunology, Biochemistry and Nutrition, Medical University of Warsaw, Poland.
Agnieszka SarneckaDepartment of Surgical Research and Transplantology, Mossakowski Medical Research Center, Polish Academy of Sciences, Warsaw, Poland.
Aleksandra DąbrowskaDepartment of Immunology, Biochemistry and Nutrition, Medical University of Warsaw, Poland.
Katarzyna KosałkaDepartment of Immunology, Biochemistry and Nutrition, Medical University of Warsaw, Poland.
Ewelina WachowskaDepartment of Immunology, Biochemistry and Nutrition, Medical University of Warsaw, Poland.
Barbara J BałanDepartment of Immunology, Biochemistry and Nutrition, Medical University of Warsaw, Poland.
Marta JankowskaDepartment of Immunology, Biochemistry and Nutrition, Medical University of Warsaw, Poland.
Teresa KortaSecond Department of Anesthesiology and Intensive Care, Medical University of Warsaw, Poland.
Grzegorz NiewińskiSecond Department of Anesthesiology and Intensive Care, Medical University of Warsaw, Poland.
Andrzej KańskiSecond Department of Anesthesiology and Intensive Care, Medical University of Warsaw, Poland.
Małgorzata Mikaszewska-SokolewiczFirst Department of Anesthesiology and Intensive Care, Medical University of Warsaw, Poland.
Mohammad OmidiDepartment of General Surgery and Nutrition, Medical University of Warsaw, Poland.
Krystyna MajewskaDepartment of General Surgery and Nutrition, Medical University of Warsaw, Poland.
Sylwia M SłotwińskaDepartment of Conservative Dentistry, Medical University of Warsaw, Poland.
Medical University of Warsaw · PLMossakowski Medical Research Institute, Polish Academy of Sciences · PLPolish Academy of Sciences · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was an attempt to determine whether the expression of genes involved in innate antibacterial response (TL R2, NOD 1, TRAF6, HMGB 1 and Hsp70) in peripheral blood leukocytes in critically ill patients, may undergo significant changes depending on the severity of the infection and the degree of malnutrition. The study was performed in a group of 128 patients with infections treated in the intensive care and surgical ward. In 103/80.5% of patients, infections had a severe course (sepsis, severe sepsis, septic shock, mechanical ventilation of the lungs). Clinical monitoring included diagnosis of severe infection (according to the criteria of the ACC P/SCC M), assessment of severity of the patient condition and risk of death (APACHE II and SAPS II), nutritional assessment (NRS 2002 and SGA scales) and the observation of the early results of treatment. Gene expression at the mRNA level was analyzed by real-time PCR. The results of the present study indicate that in critically ill patients treated in the IC U there are significant disturbances in the expression of genes associated with innate antimicrobial immunity, which may have a significant impact on the clinical outcome. The expression of these genes varies depending on the severity of the patient condition, severity of infection and nutritional status. Expression disorders of genes belonging to innate antimicrobial immunity should be diagnosed as early as possible, monitored during the treatment and taken into account during early therapeutic treatment (including early nutrition to support the functions of immune cells).

Indexed as

gene expressioninnate immunitymalnutritionsepsis

Identifiers

PMID26648775
PMCPMC4655381
OpenAlexW2418727000

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.