Evidence map›Paper›PMID 27382979›Full record

ArticleMolecular biology reports2016

The GG genotype of the -152 G/A vascular endothelial growth factor (VEGF) polymorphism predisposes to hypertension-related chronic kidney disease.

Anna Małkiewicz, Maria Skrzypkowska, Bartosz Słomiński, Janusz Siebert, Piotr Gutknecht, Jolanta Myśliwska

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Article in Molecular biology reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed, 1 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Anna MałkiewiczDepartment of Immunology, Medical University of Gdańsk, 80-211, Gdańsk, Poland. biotechnoania@gumed.edu.pl.
Maria SkrzypkowskaDepartment of Immunology, Medical University of Gdańsk, 80-211, Gdańsk, Poland.
Bartosz SłomińskiDepartment of Immunology, Medical University of Gdańsk, 80-211, Gdańsk, Poland.
Janusz SiebertDepartment of Family Medicine, Medical University of Gdańsk, 80-210, Gdańsk, Poland.
Piotr GutknechtDepartment of Family Medicine, Medical University of Gdańsk, 80-210, Gdańsk, Poland.
Jolanta MyśliwskaDepartment of Immunology, Medical University of Gdańsk, 80-211, Gdańsk, Poland.
Gdańsk Medical University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our purpose was to determine whether the VEGF -152 G/A polymorphism could be associated with chronic kidney disease and endothelial dysfunction in hypertensive patients. There were 100 healthy volunteers enrolled into the control group. The group of patients was constituted by 99 consecutively admitted hypertensive patients referred to our Institution by their general practitioner. All patients were treated with anti-hypertensive polytherapy. Presented study revealed that the hypertensive patients bearing the GG genotype were characterized by the highest values of diastolic blood pressure and markers of endothelial damage such as Angiogenin, Endostatin, CRP as well as von Willebrandt factor. In addition, higher number of immature endothelial progenitor cells with CD34(+)CD133(+), CD34(+)CD133(-) markers was observed in GG hypertensive carriers while in normotensive individuals no differences were found. Such phenomenon may indicate an increased mobilization of bone-marrow derived endothelial progenitors. It may testify to the preserved compensatory mechanism in chronic kidney disease (CKD) patients until the G3a stage of the disease. Moreover, patients with higher estimated glomerular filtration rate (eGFR) level had lower of vWf and Endostatin values, and higher level of VEGF. Taken together our findings clearly indicate the -152 GG hypertensive carriers as more prone to develop CKD. We can suspect that the VEGF -152 GG genotype is strongly associated with hypertension-dependent CKD.

Indexed as

AdultAgedCase-Control StudiesFemaleGenetic Association StudiesGenetic Predisposition to DiseaseGlomerular Filtration RateHumansHypertensionMaleMiddle AgedPolymorphism, Single NucleotideRenal Insufficiency, ChronicVascular Endothelial Growth Factor AVascular Endothelial Growth Factor AVEGFA protein, humanEndothelial precursorsKidney diseaseVEGF polymorphism

Identifiers

PMID27382979
OpenAlexW2464187978

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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.