Evidence map›Paper›PMID 26064953›Full record

ArticleBioMed research international2015

The Impact of Vitamin D3 Supplementation on Mechanisms of Cell Calcium Signaling in Chronic Kidney Disease.

Ingrid Lajdova, Viera Spustova, Adrian Oksa, Zuzana Kaderjakova, Dusan Chorvat, Marcela Morvova, Libusa Sikurova, Alzbeta Marcek Chorvatova

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2015. 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
0.8field-weighted citation impact, top 27% 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. Review
  2. Article
  3. Intracellular calcium increases in vascular smooth muscle cells with progression of chronic kidney disease in a rat model.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2017
    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

8 authors at 3 institutions in 1 country.

Ingrid LajdovaDepartment of Clinical and Experimental Pharmacology, Faculty of Medicine, Slovak Medical University, 833 03 Bratislava, Slovakia.
Viera SpustovaDepartment of Clinical and Experimental Pharmacology, Faculty of Medicine, Slovak Medical University, 833 03 Bratislava, Slovakia.
Adrian OksaDepartment of Clinical and Experimental Pharmacology, Faculty of Medicine, Slovak Medical University, 833 03 Bratislava, Slovakia.
Zuzana KaderjakovaDepartment of Nuclear Physics and Biophysics, Faculty of Mathematics, Physics and Informatics, Comenius University, 833 03 Bratislava, Slovakia.
Dusan ChorvatDepartment of Biophotonics, International Laser Centre, 833 03 Bratislava, Slovakia.
Marcela MorvovaDepartment of Nuclear Physics and Biophysics, Faculty of Mathematics, Physics and Informatics, Comenius University, 833 03 Bratislava, Slovakia.
Libusa SikurovaDepartment of Nuclear Physics and Biophysics, Faculty of Mathematics, Physics and Informatics, Comenius University, 833 03 Bratislava, Slovakia.
Alzbeta Marcek ChorvatovaDepartment of Biophotonics, International Laser Centre, 833 03 Bratislava, Slovakia.
Comenius University Bratislava · SKSlovak Medical University · SKInternational Laser Center · SK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intracellular calcium concentration in peripheral blood mononuclear cells (PBMCs) of patients with chronic kidney disease (CKD) is significantly increased, and the regulatory mechanisms maintaining cellular calcium homeostasis are impaired. The purpose of this study was to examine the effect of vitamin D3 on predominant regulatory mechanisms of cell calcium homeostasis. The study involved 16 CKD stages 2-3 patients with vitamin D deficiency treated with cholecalciferol 7000-14000 IU/week for 6 months. The regulatory mechanisms of calcium signaling were studied in PBMCs and red blood cells. After vitamin D3 supplementation, serum concentration of 25(OH)D3 increased (P < 0.001) and [Ca(2+)]i decreased (P < 0.001). The differences in [Ca(2+)]i were inversely related to differences in 25(OH)D3 concentration (P < 0.01). Vitamin D3 supplementation decreased the calcium entry through calcium release activated calcium (CRAC) channels and purinergic P2X7 channels. The function of P2X7 receptors was changed in comparison with their baseline status, and the expression of these receptors was reduced. There was no effect of vitamin D3 on P2X7 pores and activity of plasma membrane Ca(2+)-ATPases. Vitamin D3 supplementation had a beneficial effect on [Ca(2+)]i decreasing calcium entry via CRAC and P2X7 channels and reducing P2X7 receptors expression.

Indexed as

AdultAgedAged, 80 and overCalciumCalcium, DietaryCalcium SignalingCholecalciferolDietary SupplementsFemaleHumansLeukocytes, MononuclearMaleMiddle AgedReceptors, Purinergic P2X7Renal Insufficiency, ChronicVitamin D DeficiencyCalciumCalcium, DietaryCholecalciferolReceptors, Purinergic P2X7

Identifiers

PMID26064953
PMCPMC4434177
OpenAlexW1774312497

What OpenQuestion holds

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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.