Evidence map›Paper›PMID 29606859›Full record

ArticleClinical interventions in aging2018

Bogna Grygiel-Górniak, Iwona Ziółkowska-Suchanek, Elżbieta Kaczmarek, Maria Mosor, Jerzy Nowak, Mariusz Puszczewicz

Open access · goldAbstract read
In one paragraph

Article in Clinical interventions in aging, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

6 authors at 2 institutions in 1 country.

Bogna Grygiel-GórniakDepartment of Rheumatology and Internal Diseases, Poznan University of Medical Sciences, Poznan, Poland.
Iwona Ziółkowska-SuchanekInstitute of Human Genetics, Polish Academy of Sciences, Poznan, Poland.
Elżbieta KaczmarekDepartment of Bioinformatics and Computational Biology, Poznan University of Medical Sciences, Poznan, Poland.
Maria MosorInstitute of Human Genetics, Polish Academy of Sciences, Poznan, Poland.
Jerzy NowakInstitute of Human Genetics, Polish Academy of Sciences, Poznan, Poland.
Mariusz PuszczewiczDepartment of Rheumatology and Internal Diseases, Poznan University of Medical Sciences, Poznan, Poland.
Poznan University of Medical Sciences · PLInstitute of Human Genetics · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe aim of the research genetic study was to investigate the association between variants (C1431T and Pro12Ala) of the peroxisome proliferator-activated receptor (

methodsAnthropometric and biochemical parameters were measured by routine methods, followed by genotyping (TagMan

resultsAlthough there were no differences between alleles and genotypes prevalence between CTD vs control groups, interesting lipid-gene associations were noted in this study. A higher level of triglycerides (TAG) and TAG/high-density lipoprotein (HDL) ratios was observed in CTD patients compared to controls. Similar differences were noted in CTD and control groups without statin treatment. Atherogenic markers: the atherogenic index of plasma, TAG/HDL and low-density lipoprotein/HDL ratio were low in the analyzed groups. Of the six analyzed polymorphisms, the Pro12Pro or C14131C or Trp64Trp genotypes were related to higher TAG and TAG/HDL ratios in patients with CTD; however, the highest TAG values were observed in the presence of the Trp64Trp genotype.

conclusionLipid disorders were present in both groups independent of statin treatment (mixed dyslipidemia and hypercholesterolemia were observed in the CTD and control groups, respectively). The risk of dyslipidemia increases with age. The presence of Pro12Pro, C14131C and Trp64Trp genotypes is related to higher TAG level in CTDs, and of these the Trp64Trp variant most reliably predicts hypertriglyceridemia.

Indexed as

AdultAgedAllelesCase-Control StudiesConnective Tissue DiseasesDyslipidemiasGenotypeHumansHydroxymethylglutaryl-CoA Reductase InhibitorsLipoproteins, HDLLipoproteins, LDLMiddle AgedPolandPolymorphism, GeneticPPAR gammaReceptors, Adrenergic, beta-3ADRB3 protein, humanHydroxymethylglutaryl-CoA Reductase InhibitorsLipoproteins, HDLLipoproteins, LDLPPAR gammaReceptors, Adrenergic, beta-3TriglyceridesC1431TlipoproteinsPro12Alarheumatic diseasesstatinsTrp64Arg polymorphisms

Identifiers

PMID29606859
PMCPMC5868601
OpenAlexW2790342058

What OpenQuestion holds

Texttitle and abstract
LicenceCC BY-NC
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.