Evidence map›Paper›PMID 25296717›Full record

ArticleJournal of human hypertension2015

Quantitative and functional characteristics of endothelial progenitor cells in newly diagnosed hypertensive patients.

M Skrzypkowska, J Myśliwska, B Słomiński, J Siebert, P Gutknecht, M Ryba-Stanisławowska

Abstract read
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In one paragraph

Article in Journal of human hypertension, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Preserved endothelial progenitor cell angiogenic activity in African American essential hypertensive patients.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2018
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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.

M SkrzypkowskaDepartment of Immunology, Faculty of Medicine, Medical University of Gdańsk, Gdańsk, Poland.
J MyśliwskaDepartment of Immunology, Faculty of Medicine, Medical University of Gdańsk, Gdańsk, Poland.
B SłomińskiDepartment of Immunology, Faculty of Medicine, Medical University of Gdańsk, Gdańsk, Poland.
J SiebertDepartment of Family Medicine, Faculty of Medicine, Medical University of Gdańsk, Gdańsk, Poland.
P GutknechtDepartment of Family Medicine, Faculty of Medicine, Medical University of Gdańsk, Gdańsk, Poland.
M Ryba-StanisławowskaDepartment of Immunology, Faculty of Medicine, Medical University of Gdańsk, Gdańsk, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Populations of peripheral blood CD34(+) cells comprise precursors of endothelial cells. These precursors are crucial to cardiovascular homeostasis. Hypertension, as one of the main risk factors for cardiovascular disease, is associated with the loss of endothelium structural integrity and its functional impairment. The aim of our study was to evaluate the subsets of endothelial precursor cells in patients with newly diagnosed arterial hypertension. Twenty-four newly diagnosed, previously untreated hypertensive patients aged 59.5 ± 12.5 years, were enrolled into the study group, whereas the control group comprised 45 healthy subjects, 55.5±10.0 years old. Endothelial progenitor cells (EPCs) were analysed by flow cytometry. The results showed that hypertensive patients were characterized by a significantly higher percentage and number of the CD34(+) cells and simultaneously less differentiated CD34(+)CD45(dim/neg)CD133(+) progenitors. The percentage and number of CD34(+)CD45(neg)VEGFR2(+) and CD34(+)CD45(neg)CD133(+)VEGFR2(+) cells were not different from the control group. Moreover, patients had a significantly lower percentage and number of the CD34(+)CD45(neg)VEGFR2(+)CXCR4(+) and CD34(+)CD45(neg)VEGFR2(+)ICAM-1(+) cells than healthy individuals. These changes were paralleled by early symptoms of nephropathy, that is, lower glomerular filtration rate (GFR) values and borderline micro albuminuria. Our results indicate that an elevation in the number of less differentiated progenitors may be a mechanism compensating for defects of migration and adhesion, present in a more differentiated subset.

Indexed as

HypertensionAgedAntigens, CD34Blood Pressure DeterminationCell AdhesionCell MovementEndothelial Progenitor CellsEndothelium, VascularFemaleFlow CytometryGlomerular Filtration RateHumansIntercellular Adhesion Molecule-1MaleMiddle AgedReceptors, CXCR4Antigens, CD34Intercellular Adhesion Molecule-1Receptors, CXCR4Vascular Endothelial Growth Factor Receptor-2

Identifiers

PMID25296717

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.