Evidence map›Paper›PMID 35744013›Full record

ArticleMedicina (Kaunas, Lithuania)2022

Georgia Matthiopoulou, Maria I Zervou, Chrysoula Stathopoulou, Petros Ioannou, John A Papadakis, Vasiliki N Daraki, Angelos Pappas, Sotiris Souris, George Samonis, George N Goulielmos and 1 more

Open access · goldAbstract read
In one paragraph

Article in Medicina (Kaunas, Lithuania), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 91% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

11 authors at 4 institutions in 1 country.

Georgia MatthiopoulouFirst Department of Internal Medicine, General Hospital of Heraklion Venizeleion, 71409 Heraklion, Greece.
Maria I ZervouSection of Molecular Pathology and Human Genetics, Department of Internal Medicine, School of Medicine, University of Crete, 71003 Heraklion, Greece.
Chrysoula StathopoulouLaboratory of Rheumatology, Autoimmunity and Inflammation, Institute of Molecular Biology and Biotechnology, FORTH, 70013 Heraklion, Greece.
Petros IoannouDepartment of Internal Medicine & Infectious Diseases, University Hospital of Heraklion, 71110 Heraklion, Greece.ORCID 0000-0003-1082-5674
John A PapadakisDepartment of Internal Medicine & Infectious Diseases, University Hospital of Heraklion, 71110 Heraklion, Greece.
Vasiliki N DarakiDepartment of Endocrinology, University Hospital of Heraklion, 71110 Heraklion, Greece.
Angelos PappasDiabetes Unit, General Hospital of Heraklion Venizeleion, 71409 Heraklion, Greece.
Sotiris SourisFirst Department of Internal Medicine, General Hospital of Heraklion Venizeleion, 71409 Heraklion, Greece.
George SamonisDepartment of Internal Medicine & Infectious Diseases, University Hospital of Heraklion, 71110 Heraklion, Greece.
George N GoulielmosSection of Molecular Pathology and Human Genetics, Department of Internal Medicine, School of Medicine, University of Crete, 71003 Heraklion, Greece.ORCID 0000-0002-9797-2310
Diamantis P KofteridisDepartment of Internal Medicine & Infectious Diseases, University Hospital of Heraklion, 71110 Heraklion, Greece.ORCID 0000-0003-0255-5926
University Hospital of Heraklion · GRUniversity of Crete · GRThe General Hospital of Heraklion "Venizeleio-Pananio" · GRFORTH Institute of Molecular Biology and Biotechnology · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Objectives: Asymptomatic bacteriuria (ASB) appears to have a higher prevalence in diabetics and has been associated with various genetic polymorphisms of the innate immune system. Single nucleotide polymorphisms (SNPs) of the C1q gene that encodes for the trigger molecule of the classical complement pathway increase the risk of bacterial infections as well as other diseases. In the present study, we sought to investigate the association of C1q rs292001 (G > A) SNP with ASB in patients with type 2 diabetes (T2D). Materials and Methods: In this case-control study, performed at the University and the Venizeleion General Hospital of Heraklion, Crete, Greece, 75 adult male and female Cretan patients with T2D and ASB and 75 adult male and female Cretan patients with T2D but without ASB were enrolled and genotyped for rs292001 SNP of C1q gene. Genetic analysis was based on the polymerase chain reaction (PCR) and restriction fragment length polymorphisms (RLFPs) methods. Results: Τhe frequency of homozygotes for the G/G genotype of C1q rs292001 was significantly higher in patients with T2D and ASB than in the control group (p-value = 0.0480, OR = 2.952, 95% CI: 1.052−7.542). Conclusions: Τhe present study provides the first evidence of an association between the C1q rs292001 SNP and an increased susceptibility for ASB in an adult Cretan population with T2D, thus suggesting that this SNP can be encountered as a risk factor for the presence of ASB in patients with T2D.

Indexed as

BacteriuriaDiabetes Mellitus, Type 2AdultCase-Control StudiesComplement C1qFemaleGenetic Predisposition to DiseaseHumansMalePolymorphism, Single NucleotideComplement C1qasymptomatic bacteriuriaC1qgene polymorphisminnate immunitytype 2 diabetes

Identifiers

PMID35744013
PMCPMC9230576
OpenAlexW4281887754

What OpenQuestion holds

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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.