Evidence mapPaperPMID 35205271Full record

ArticleGenes2022

Marco Guarneri, Letizia Scola, Rosa Maria Giarratana, Manuela Bova, Caterina Carollo, Loredana Vaccarino, Leonardo Calandra, Domenico Lio, Carmela Rita Balistreri, Santina Cottone

Open access · goldAbstract read
In one paragraph

Article in Genes, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 33% 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

10 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
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  9. Genes · 2022
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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

10 authors at 2 institutions in 1 country.

Marco GuarneriUnit of Nephrology & Hypertension, European Society of Hypertension Excellence Center, Department of Health Promotion Sciences, Maternal & Infant Care, Internal Medicine & Medical Specialties (PROMISE), University of Palermo, "Paolo Giaccone" University Hospital, 90127 Palermo, Italy.ORCID 0000-0002-2827-8245
Letizia ScolaClinical Pathology, Department of Bio-Medicine, Neuroscience, and Advanced Diagnostics, University of Palermo, 90100 Palermo, Italy.
Rosa Maria GiarratanaClinical Pathology, Department of Bio-Medicine, Neuroscience, and Advanced Diagnostics, University of Palermo, 90100 Palermo, Italy.
Manuela BovaClinical Pathology, Department of Bio-Medicine, Neuroscience, and Advanced Diagnostics, University of Palermo, 90100 Palermo, Italy.
Caterina CarolloUnit of Nephrology & Hypertension, European Society of Hypertension Excellence Center, Department of Health Promotion Sciences, Maternal & Infant Care, Internal Medicine & Medical Specialties (PROMISE), University of Palermo, "Paolo Giaccone" University Hospital, 90127 Palermo, Italy.
Loredana VaccarinoClinical Pathology, Department of Bio-Medicine, Neuroscience, and Advanced Diagnostics, University of Palermo, 90100 Palermo, Italy.
Leonardo CalandraUnit of Nephrology & Hypertension, European Society of Hypertension Excellence Center, Department of Health Promotion Sciences, Maternal & Infant Care, Internal Medicine & Medical Specialties (PROMISE), University of Palermo, "Paolo Giaccone" University Hospital, 90127 Palermo, Italy.ORCID 0000-0003-0127-4751
Domenico LioClinical Pathology, Department of Bio-Medicine, Neuroscience, and Advanced Diagnostics, University of Palermo, 90100 Palermo, Italy.ORCID 0000-0003-4550-1389
Carmela Rita BalistreriClinical Pathology, Department of Bio-Medicine, Neuroscience, and Advanced Diagnostics, University of Palermo, 90100 Palermo, Italy.ORCID 0000-0002-5393-1007
Santina CottoneUnit of Nephrology & Hypertension, European Society of Hypertension Excellence Center, Department of Health Promotion Sciences, Maternal & Infant Care, Internal Medicine & Medical Specialties (PROMISE), University of Palermo, "Paolo Giaccone" University Hospital, 90127 Palermo, Italy.
University of Palermo · ITEuropean Society of Hypertension · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic kidney disease (CKD) is characterized by an increased risk of kidney failure and end-stage renal disease (ESRD). Aging and comorbidities as cardiovascular diseases, metabolic disorders, infectious diseases, or tumors, might increase the risk of dialysis. In addition, genetic susceptibility factors might modulate kidney damage evolution. We have analyzed, in a group of ESRD patients and matched controls, a set of SNPs of genes (

Indexed as

Interleukin-6Kidney Failure, ChronicMacrophage Migration-Inhibitory FactorsCase-Control StudiesFemaleGene FrequencyGenetic Predisposition to DiseaseHumansIntramolecular OxidoreductasesKidneyMaleMiddle AgedPolymorphism, Single NucleotideIL6 protein, humanInterleukin-6Intramolecular OxidoreductasesMacrophage Migration-Inhibitory FactorsMIF protein, humanCKDESRDIL6MIFSNP

Identifiers

PMID35205271
PMCPMC8872268
OpenAlexW4210809150

What Socratic 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 Socratic graph.