Evidence map›Paper›PMID 41683831›Full record

ArticleInternational journal of molecular sciences2026

Role of Inositol Hexakisphosphate Kinases in Vascular Smooth Muscle Cell Calcification.

Sheyda Bahiraii, Isratul Jannat, Sarah Plösser, Mehdi Razazian, Jakob Voelkl, Ioana Alesutan

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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

1 citing paper in PubMed.

  1. Review
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.

Sheyda BahiraiiInstitute for Physiology and Pathophysiology, Johannes Kepler University Linz, Altenbergerstrasse 69, 4040 Linz, Austria.
Isratul JannatInstitute for Physiology and Pathophysiology, Johannes Kepler University Linz, Altenbergerstrasse 69, 4040 Linz, Austria.
Sarah PlösserInstitute for Physiology and Pathophysiology, Johannes Kepler University Linz, Altenbergerstrasse 69, 4040 Linz, Austria.
Mehdi RazazianInstitute for Physiology and Pathophysiology, Johannes Kepler University Linz, Altenbergerstrasse 69, 4040 Linz, Austria.ORCID 0000-0001-8806-6773
Jakob VoelklInstitute for Physiology and Pathophysiology, Johannes Kepler University Linz, Altenbergerstrasse 69, 4040 Linz, Austria.
Ioana AlesutanInstitute for Physiology and Pathophysiology, Johannes Kepler University Linz, Altenbergerstrasse 69, 4040 Linz, Austria.

Funding

Austrian Science Fund (FWF) 10.55776/P34724
6 · The paper itself

Abstract

Phosphate-induced vascular calcification in chronic kidney disease is linked to cardiovascular mortality. This calcification process involves vascular smooth muscle cells (VSMCs), which can promote a pro-calcific environment in the vascular wall. However, the mechanisms underlying a putative phosphate sensing of VSMCs to modulate pro-calcific signaling are insufficiently clarified. In mammals, three isoforms of the inositol hexakisphosphate kinase (IP6K) exist, which have been implicated in cellular phosphate homeostasis. Therefore, each IP6K isoform was silenced in calcifying primary human aortic VSMCs.

Indexed as

Muscle, Smooth, VascularMyocytes, Smooth MusclePhosphotransferases (Phosphate Group Acceptor)Vascular CalcificationCells, CulturedHumansPhosphatesPhosphorylationProto-Oncogene Proteins c-aktSignal Transductioninositol hexakisphosphate kinasePhosphatesPhosphotransferases (Phosphate Group Acceptor)Proto-Oncogene Proteins c-akt5-IP7AKTchronic kidney diseaseinositol hexakisphosphate kinaseIP6KphosphateSGK1vascular calcificationvascular smooth muscle cells

Identifiers

PMID41683831
PMCPMC12897964

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.