Evidence map›Paper›PMID 28808355›Full record

ArticleDisease markers2017

New Markers of Inflammation and Tubular Damage in Children with Chronic Kidney Disease.

Kinga Musiał, Agnieszka Bargenda, Dorota Drożdż, Danuta Zwolińska

Open access · hybridAbstract read
In one paragraph

Article in Disease markers, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

8 citing papers in PubMed, 18 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

4 authors at 2 institutions in 1 country.

Kinga MusiałDepartment of Pediatric Nephrology, Wrocław Medical University, Wrocław, Poland.ORCID 0000-0002-9000-7585
Agnieszka BargendaDepartment of Pediatric Nephrology, Wrocław Medical University, Wrocław, Poland.
Dorota DrożdżDepartment of Pediatric Nephrology, Jagiellonian University, Kraków, Poland.ORCID 0000-0002-1281-1164
Danuta ZwolińskaDepartment of Pediatric Nephrology, Wrocław Medical University, Wrocław, Poland.
Wroclaw Medical University · PLJagiellonian University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

INTRODUCTION AND

aimsMonocyte chemoattractant protein- (MCP-) 1, macrophage colony-stimulating factor (MCSF), and neopterin are connected with monocyte migration and transition into macrophages, leading to fibrosis and tubular damage in the course of CKD. The aim of the study was to analyze the applicability of urinary fractional excretion (FE) of MCP1, MCSF, and neopterin, as markers of inflammation and tubular damage, in children with CKD.

methodsThe study group consisted of 61 children with CKD stages 1-5 and 23 age-matched controls. The serum and urine concentrations of MCP1, MCSF, and neopterin were assessed by ELISA and then the fractional excretion (FE) was calculated.

resultsFE MCSF and neopterin values exceeded 1% already in controls. FE MCSF rose significantly since CKD stages 1-2, FE neopterin since CKD stages 3-5. FE MCP1 was below 1% in healthy controls and in CKD stages 1-2, then increased significantly in CKD stages 3-5.

conclusionsThe FE MCP-1 values show that inflammation precedes the tubular dysfunction. FE MCSF and FE neopterin may be considered new markers of the renal parenchyma progressive damage. Fractional excretion may become a useful tool in the assessment of inflammation and tubular damage in children with CKD.

Indexed as

AdolescentBiomarkersCase-Control StudiesChemokine CCL2ChildFemaleHumansKidney TubulesMacrophage Colony-Stimulating FactorMaleNeopterinRenal Insufficiency, ChronicBiomarkersCCL2 protein, humanChemokine CCL2Macrophage Colony-Stimulating FactorNeopterin

Identifiers

PMID28808355
PMCPMC5541796
OpenAlexW2739185722

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.