Evidence map›Paper›PMID 29315078›Full record

ArticleAging2018

Associations between the components of metabolic syndrome and the polymorphisms in the peroxisome proliferator-activated receptor gamma (

Małgorzata Szkup, Aleksander Jerzy Owczarek, Daria Schneider-Matyka, Jacek Brodowski, Beata Łój, Elżbieta Grochans

Open access · greenAbstract read
In one paragraph

Article in Aging, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 2 pooled it
0.6field-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

13 citing papers in PubMed, 2 syntheses or guidelines pooled it, 19 citations in OpenAlex.

  1. Pooled it
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  13. PPARInternational journal of nephrology · 2020
    Review
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

6 authors at 3 institutions in 2 countries.

Małgorzata SzkupDepartment of Nursing, Pomeranian Medical University in Szczecin, Szczecin, 71-210, Poland.
Aleksander Jerzy OwczarekDepartment of Statistics, Department of Instrumental Analysis, School of Pharmacy with the Division of Laboratory Medicine in Sosnowiec, Medical University of Silesia, Katowice, Sosnowiec, 41-200, Poland.
Daria Schneider-MatykaDepartment of Nursing, Pomeranian Medical University in Szczecin, Szczecin, 71-210, Poland.
Jacek BrodowskiPrimary Care Department, Pomeranian Medical University in Szczecin, Szczecin, 71-210, Poland.
Beata ŁójKlinik für Gynäkologie und Geburtshilfe, Sana HANSE-Klinikum Wismar GmbH, Wismar, 23966, Germany.
Elżbieta GrochansDepartment of Nursing, Pomeranian Medical University in Szczecin, Szczecin, 71-210, Poland.
Pomeranian Medical University · PLMedical University of Silesia · PLWismar University of Applied Sciences · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMetabolic syndrome (MetS) is regarded as a set of abnormalities, increasing the risk of serious functioning disorders. It can develop as a result of genetic predisposition.

aimThe aim of this study was to establish associations between MetS-related abnormalities and the MATERIAL AND

methodsThe study involved 425 women aged 45-60 years. The participants were surveyed and subjected to anthropometric, biochemical and genetic analysis.

resultsIn the recessive inheritance model for the

conclusions1. MetS-related abnormalities can be genetically determined, however only some of these relationships can be demonstrated due to the categorical division of symptoms according to the IDF criteria from 2009. 2. The A/A genotype of the

Indexed as

Alpha-Ketoglutarate-Dependent Dioxygenase FTOBlood PressureFemaleGenetic Association StudiesGenetic Predisposition to DiseaseHumansHyperglycemiaHypertriglyceridemiaMetabolic SyndromeMiddle AgedOdds RatioPolymorphism, Single NucleotidePPAR gammaReceptor, Melanocortin, Type 4Alpha-Ketoglutarate-Dependent Dioxygenase FTOFTO protein, humanMC4R protein, humanPPAR gammaReceptor, Melanocortin, Type 4FTO proteinhumanmelanocortinmetabolic syndrome XPPAR gammareceptortype 4

Identifiers

PMID29315078
PMCPMC5811243
OpenAlexW2782638761

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.