Evidence map›Paper›PMID 27698480›Full record

Observational studyScientific reports2016

Mode of renal replacement therapy determines endotoxemia and neutrophil dysfunction in chronic kidney disease.

Sandra Lemesch, Werner Ribitsch, Gernot Schilcher, Walter Spindelböck, Hildegard Hafner-Gießauf, Gunther Marsche, Lisa Pasterk, Doris Payerl, Bianca Schmerböck, Monika Tawdrous and 9 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 15% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
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  8. Oral dysbiosis initiates periodontal disease in experimental kidney disease.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2025
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  12. Disease severity and proton pump inhibitor use impact strongest on faecal microbiome composition in liver cirrhosis.Liver international : official journal of the International Association for the Study of the Liver · 2020
    Article
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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

19 authors at 1 institution in 1 country.

Sandra LemeschDepartment of Internal Medicine, Division of Gastroenterology and Hepatology, Medical University of Graz, Graz, Austria.
Werner RibitschDepartment of Internal Medicine, Clinical Division of Nephrology, Medical University of Graz, Graz, Austria.
Gernot SchilcherDepartment of Internal Medicine, Clinical Division of Nephrology, Medical University of Graz, Graz, Austria.
Walter SpindelböckDepartment of Internal Medicine, Division of Gastroenterology and Hepatology, Medical University of Graz, Graz, Austria.
Hildegard Hafner-GießaufDepartment of Internal Medicine, Clinical Division of Nephrology, Medical University of Graz, Graz, Austria.
Gunther MarscheInstitute of Experimental and Clinical Pharmacology, Medical University of Graz, Graz, Austria.
Lisa PasterkInstitute of Experimental and Clinical Pharmacology, Medical University of Graz, Graz, Austria.
Doris PayerlInstitute of Physiological Chemistry, Center of Physiological Medicine, Medical University of Graz, Graz, Austria.
Bianca SchmerböckDepartment of Surgery, Division of Transplantation Surgery, Medical University of Graz, Graz, Austria.
Monika TawdrousDepartment of Internal Medicine, Division of Gastroenterology and Hepatology, Medical University of Graz, Graz, Austria.
Alexander R RosenkranzDepartment of Internal Medicine, Clinical Division of Nephrology, Medical University of Graz, Graz, Austria.
Philipp StieglerDepartment of Surgery, Division of Transplantation Surgery, Medical University of Graz, Graz, Austria.
Gerd KagerInstitute of Physiological Chemistry, Center of Physiological Medicine, Medical University of Graz, Graz, Austria.
Seth HallströmInstitute of Physiological Chemistry, Center of Physiological Medicine, Medical University of Graz, Graz, Austria.
Karl OettlInstitute of Physiological Chemistry, Center of Physiological Medicine, Medical University of Graz, Graz, Austria.
Katharina EberhardCore Facility Computational Bioanalytics, Center for Medical Research, Medical University of Graz, Graz, Austria.
Angela HorvathDepartment of Internal Medicine, Division of Gastroenterology and Hepatology, Medical University of Graz, Graz, Austria.
Bettina LeberDepartment of Surgery, Division of Transplantation Surgery, Medical University of Graz, Graz, Austria.
Vanessa StadlbauerDepartment of Internal Medicine, Division of Gastroenterology and Hepatology, Medical University of Graz, Graz, Austria.
Medical University of Graz · AT

Funding

Austrian Science Fund FWF W 1241
6 · The paper itself

Abstract

Bacterial infection and sepsis are common complications of chronic kidney disease (CKD). A vicious cycle of increased gut permeability, endotoxemia, inadequate activation of the innate immune system and resulting innate immune dysfunction is hypothesized. We assessed endotoxemia, neutrophil function and its relation to oxidative stress, inflammation and gut permeability in patients with CKD grade 3-5 without renal replacement therapy (CKD group, n = 57), patients with CKD stage 5 undergoing haemodialysis (HD, n = 32) or peritoneal dialysis (PD, n = 28) and patients after kidney transplantation (KT, n = 67) in a cross-sectional observational study. In HD patients, endotoxin serum levels were elevated and neutrophil phagocytic capacity was decreased compared to all other groups. Patients on HD had a significantly higher mortality, due to infections during follow up, compared to PD (p = 0.022). Oxidative stress, neutrophil energy charge, systemic inflammation and gut permeability could not completely explain these differences. Our findings suggest that dialysis modality and not renal function per se determine the development of neutrophil dysfunction and endotoxemia in CKD-patients. HD patients are particularly prone to neutrophil dysfunction and endotoxemia whereas neutrophil function seems to improve after KT. Multi-target approaches are therefore warranted to improve neutrophil function and potentially reduce the rate of infections with patients undergoing haemodialysis.

Indexed as

Renal Replacement TherapyAdultAgedAged, 80 and overBacterial InfectionsCross-Sectional StudiesEndotoxemiaFemaleHumansMaleMiddle AgedNeutrophilsOxidative StressRenal Insufficiency, Chronic

Identifiers

PMID27698480
PMCPMC5048306
OpenAlexW2529300699

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.