Evidence map›Paper›PMID 41081331›Full record

ArticleFEBS open bio2026

Diabetes-induced vascular calcification is associated with low pyrophosphate and its oral supplementation prevents calcification in diabetic mice.

Krisztina Fülöp, Eszter Kozák, Natália Tőkési, Lilian Kocsis, Anikó Kelemen, Zsuzsanna Geszti, Adriána Kutás, Mariann Harangi, Ágnes Diószegi, Zsolt Rapi and 4 more

Abstract read
In one paragraph

Article in FEBS open bio, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

14 authors.

Krisztina FülöpInstitute of Molecular Life Sciences, Research Centre for Natural Sciences, Centre of Excellence of the Hungarian Academy of Sciences, HUN-REN, Budapest, Hungary.
Eszter KozákInstitute of Molecular Life Sciences, Research Centre for Natural Sciences, Centre of Excellence of the Hungarian Academy of Sciences, HUN-REN, Budapest, Hungary.
Natália TőkésiInstitute of Molecular Life Sciences, Research Centre for Natural Sciences, Centre of Excellence of the Hungarian Academy of Sciences, HUN-REN, Budapest, Hungary.
Lilian KocsisInstitute of Molecular Life Sciences, Research Centre for Natural Sciences, Centre of Excellence of the Hungarian Academy of Sciences, HUN-REN, Budapest, Hungary.
Anikó KelemenInstitute of Molecular Life Sciences, Research Centre for Natural Sciences, Centre of Excellence of the Hungarian Academy of Sciences, HUN-REN, Budapest, Hungary.
Zsuzsanna GesztiInstitute of Molecular Life Sciences, Research Centre for Natural Sciences, Centre of Excellence of the Hungarian Academy of Sciences, HUN-REN, Budapest, Hungary.
Adriána KutásInstitute of Molecular Life Sciences, Research Centre for Natural Sciences, Centre of Excellence of the Hungarian Academy of Sciences, HUN-REN, Budapest, Hungary.
Mariann HarangiDivision of Metabolism, Department of Internal Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Ágnes DiószegiDivision of Metabolism, Department of Internal Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Zsolt RapiDepartment of Organic Chemistry and Technology, Budapest University of Technology and Economics, Budapest, Hungary.
József BallaVascular Pathophysiology Research Group 11003, University of Debrecen, HUN-REN, Debrecen, Hungary.
Olivier Le SauxDepartment of Cell and Molecular Biology, John A. Burns School of Medicine, University of Hawaii, Honolulu, HI, USA.
András VáradiInstitute of Molecular Life Sciences, Research Centre for Natural Sciences, Centre of Excellence of the Hungarian Academy of Sciences, HUN-REN, Budapest, Hungary.
Viola PomoziInstitute of Molecular Life Sciences, Research Centre for Natural Sciences, Centre of Excellence of the Hungarian Academy of Sciences, HUN-REN, Budapest, Hungary.ORCID https://orcid.org/0000-0002-5435-4993

Funding

TRPA1 Physiology in Diabetes, Metabolic Syndrome, and MetabolismP20GM113134 · NIGMS · UNIVERSITY OF HAWAII AT MANOA · PI Kathryn Jaques Schunke · 2017 to 2026
$21.5M
Hungarian Research Network ELKH-POC-2022-011National Research, Development and Innovation Office of Hungary K-OTKA 127933National Research, Development and Innovation Office of Hungary K-OTKA 127957National Research, Development and Innovation Office of Hungary PD-OTKA 128003NIH HHS P20GM113134
6 · The paper itself

Abstract

The predominant cause of death among diabetic patients comes from cardiovascular complications, including vascular calcification. The objectives of this study were to improve the understanding of the molecular mechanisms involved in diabetes-related calcification and to test potential preventive therapies. We found that levels of plasma pyrophosphate-a potent inhibitor of calcification-were decreased in type 1 and type 2 diabetic patients with cardiovascular symptoms. To further investigate vascular calcification, we developed a diabetic mouse model that showed increased aorta and renal calcification compared to control. Alkaline phosphatase activity was also increased in the circulation of diabetic mice, which resulted in a significant decrease in plasma pyrophosphate. Oral treatment with pyrophosphate prevented diabetes-induced calcification in mice, providing a direct translational value for clinical applications.

Indexed as

Diabetes Mellitus, ExperimentalDiphosphatesVascular CalcificationAdministration, OralAlkaline PhosphataseAnimalsDiabetes Mellitus, Type 1Diabetes Mellitus, Type 2Dietary SupplementsDisease Models, AnimalFemaleHumansMaleMiceMice, Inbred C57BLAlkaline PhosphataseDiphosphatesdiphosphoric acidcardiovascular calcificationdiabetesmouse modelpyrophosphate

Identifiers

PMID41081331
PMCPMC12955752

What OpenQuestion holds

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Registered trials

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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.