Evidence map›Paper›PMID 27671905›Full record

ArticleInternational urology and nephrology2016

Association between functional variant of inflammatory system gene (PSMA6) and end-stage kidney disease.

Monika Buraczynska, Anna Stec, Aleksandra Filipczak, Andrzej Ksiazek

Open access · hybridAbstract read
In one paragraph

Article in International urology and nephrology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 31% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Whole-Genome and Poly(A)+Transcriptome Analysis of theInternational journal of molecular sciences · 2024
    Article
  3. Article
  4. Article
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 1 institution in 1 country.

Monika BuraczynskaDepartment of Nephrology, Medical University of Lublin, Jaczewskiego 8, 20-954, Lublin, Poland. monika.buraczynska@umlub.pl.
Anna StecDepartment of Nephrology, Medical University of Lublin, Jaczewskiego 8, 20-954, Lublin, Poland.
Aleksandra FilipczakDepartment of Nephrology, Medical University of Lublin, Jaczewskiego 8, 20-954, Lublin, Poland.
Andrzej KsiazekDepartment of Nephrology, Medical University of Lublin, Jaczewskiego 8, 20-954, Lublin, Poland.
Medical University of Lublin · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe proteasome system is involved in several disorders. The 5' untranslated region of PSMA6 gene contains a single nucleotide polymorphism (SNP) -8 C/G, associated with diabetes, myocardial infarction and coronary artery disease.

methodsWe examined 584 patients with end-stage kidney disease (ESKD) and 430 controls. All were genotyped for -8 C/G SNP by polymerase chain reaction and restriction analysis.

resultsWe observed lower frequency of CG + GG genotypes in patients than in controls (20 vs. 42 %, p = 0.0038). The odds ratio of 0.34 (95 % CI 0.26-0.45) suggests association of CG + GG with decreased risk of ESKD. We investigated the association between PSMA6 polymorphism and LVH present in 54 % of patients. There was a significant association of CG + GG genotype with LVH, with over 75 % of CG + GG in patients with LVH. This effect was independent from other common causes of LVH-age (OR 1.12, p = 0.643) and hypertension (OR 1.72, p = 0.422).

conclusionWe demonstrated for the first time that PSMA6 polymorphism might be a protective factor for ESKD. On the other hand, CG + GG genotypes are independently related to LVH in ESKD patients.

Indexed as

AdultAgedFemaleGene FrequencyGenetic Predisposition to DiseaseHumansHypertensionHypertrophy, Left VentricularKidney Failure, ChronicMaleMiddle AgedPolandPolymorphism, Single NucleotideProteasome Endopeptidase ComplexProtective FactorsProteasome Endopeptidase ComplexPSMA6 protein, humanEnd-stage renal diseaseGenotypingLVHPSMA6Single nucleotide polymorphism

Identifiers

PMID27671905
PMCPMC5099367
OpenAlexW2524878053

What OpenQuestion holds

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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.