Evidence map›Paper›PMID 30271792›Full record

ReviewJournal of immunology research2018

Inflammation-Related Mechanisms in Chronic Kidney Disease Prediction, Progression, and Outcome.

Simona Mihai, Elena Codrici, Ionela Daniela Popescu, Ana-Maria Enciu, Lucian Albulescu, Laura Georgiana Necula, Cristina Mambet, Gabriela Anton, Cristiana Tanase

Open access · goldAbstract readReview
In one paragraph

Review in Journal of immunology research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 389 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
389citing papers in PubMed, 5 pooled it
17.2field-weighted citation impact, top 1% 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

389 citing papers in PubMed, 5 syntheses or guidelines pooled it, 643 citations in OpenAlex.

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  10. GLP-1 receptor agonists-a potential therapy for chronic kidney disease?Clinical science (London, England : 1979) · 2026
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329 more citing papers are in PubMed but not listed here.

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

9 authors at 3 institutions in 1 country.

Simona MihaiVictor Babes National Institute of Pathology, 050096 Bucharest, Romania.ORCID 0000-0001-5624-2058
Elena CodriciVictor Babes National Institute of Pathology, 050096 Bucharest, Romania.
Ionela Daniela PopescuVictor Babes National Institute of Pathology, 050096 Bucharest, Romania.ORCID 0000-0001-8751-0043
Ana-Maria EnciuVictor Babes National Institute of Pathology, 050096 Bucharest, Romania.ORCID 0000-0002-8122-1096
Lucian AlbulescuVictor Babes National Institute of Pathology, 050096 Bucharest, Romania.ORCID 0000-0002-8838-2642
Laura Georgiana NeculaVictor Babes National Institute of Pathology, 050096 Bucharest, Romania.
Cristina MambetStefan S. Nicolau Institute of Virology, Molecular Virology Department, 030304 Bucharest, Romania.
Gabriela AntonStefan S. Nicolau Institute of Virology, Molecular Virology Department, 030304 Bucharest, Romania.
Cristiana TanaseVictor Babes National Institute of Pathology, 050096 Bucharest, Romania.ORCID 0000-0002-2122-0235
Institutul National Victor Babes · ROCarol Davila University of Medicine and Pharmacy · ROTitu Maiorescu University · RO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Persistent, low-grade inflammation is now considered a hallmark feature of chronic kidney disease (CKD), being involved in the development of all-cause mortality of these patients. Although substantial improvements have been made in clinical care, CKD remains a major public health burden, affecting 10-15% of the population, and its prevalence is constantly growing. Due to its insidious nature, CKD is rarely diagnosed in early stages, and once developed, its progression is unfortunately irreversible. There are many factors that contribute to the setting of the inflammatory status in CKD, including increased production of proinflammatory cytokines, oxidative stress and acidosis, chronic and recurrent infections, altered metabolism of adipose tissue, and last but not least, gut microbiota dysbiosis, an underestimated source of microinflammation. In this scenario, a huge step forward was made by the increasing progression of omics approaches, specially designed for identification of biomarkers useful for early diagnostic and follow-up. Recent omics advances could provide novel insights in deciphering the disease pathophysiology; thus, identification of circulating biomarker panels using state-of-the-art proteomic technologies could improve CKD early diagnosis, monitoring, and prognostics. This review aims to summarize the recent knowledge regarding the relationship between inflammation and CKD, highlighting the current proteomic approaches, as well as the inflammasomes and gut microbiota dysbiosis involvement in the setting of CKD, culminating with the troubling bidirectional connection between CKD and renal malignancy, raised on the background of an inflammatory condition.

Indexed as

BiomarkersCytokinesDisease ProgressionGastrointestinal MicrobiomeHumansInflammationOxidative StressPredictive Value of TestsPrognosisProteomicsRenal Insufficiency, ChronicTreatment OutcomeBiomarkersCytokines

Identifiers

PMID30271792
PMCPMC6146775
OpenAlexW2890296042

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.