Evidence map›Paper›PMID 36136575›Full record

SynthesisToxins2022

Serum Calcification Propensity Represents a Good Biomarker of Vascular Calcification: A Systematic Review.

Maxime Pluquet, Said Kamel, Gabriel Choukroun, Sophie Liabeuf, Solène M Laville

Open access · goldAbstract readSystematic Review
In one paragraph

Synthesis in Toxins, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

19 citing papers in PubMed, 25 citations in OpenAlex.

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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

5 authors at 2 institutions in 1 country.

Maxime PluquetMP3CV Laboratory, EA7517, Jules Verne University of Picardie, F-80000 Amiens, France.ORCID 0000-0003-4330-2925
Said KamelMP3CV Laboratory, EA7517, Jules Verne University of Picardie, F-80000 Amiens, France.
Gabriel ChoukrounMP3CV Laboratory, EA7517, Jules Verne University of Picardie, F-80000 Amiens, France.
Sophie LiabeufMP3CV Laboratory, EA7517, Jules Verne University of Picardie, F-80000 Amiens, France.ORCID 0000-0001-5384-9006
Solène M LavilleMP3CV Laboratory, EA7517, Jules Verne University of Picardie, F-80000 Amiens, France.ORCID 0000-0002-0214-5567
Centre Hospitalier Universitaire Amiens-Picardie · FRMécanismes physiopathologiques et conséquences des calcifications cardiovasculaires · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vascular calcification contributes to cardiovascular morbidity and mortality. A recently developed serum calcification propensity assay is based on the half-transformation time (T50) from primary calciprotein particles (CPPs) to secondary CPPs, reflecting the serum's endogenous capacity to prevent calcium phosphate precipitation. We sought to identify and review the results of all published studies since the development of the T50-test by Pasch et al. in 2012 (whether performed in vitro, in animals or in the clinic) of serum calcification propensity. To this end, we searched PubMed, Elsevier EMBASE, the Cochrane Library and Google Scholar databases from 2012 onwards. At the end of the selection process, 57 studies were analyzed with regard to the study design, sample size, characteristics of the study population, the intervention and the main results concerning T50. In patients with primary aldosteronism, T50 is associated with the extent of vascular calcification in the abdominal aorta. In chronic kidney disease (CKD), T50 is associated with the severity and progression of coronary artery calcification. T50 is also associated with cardiovascular events and all-cause mortality in CKD patients, patients on dialysis and kidney transplant recipients and with cardiovascular mortality in patients on dialysis, kidney transplant recipients, patients with ischemic heart failure and reduced ejection fraction, and in the general population. Switching from acetate-acidified dialysate to citrate-acidified dialysate led to a longer T50, as did a higher dialysate magnesium concentration. Oral administration of magnesium (in CKD patients), phosphate binders, etelcalcetide and spironolactone (in hemodialysis patients) was associated with a lower serum calcification propensity. Serum calcification propensity is an overall marker of calcification associated with hard outcomes but is currently used in research projects only. This assay might be a valuable tool for screening serum calcification propensity in at-risk populations (such as CKD patients and hemodialyzed patients) and, in particular, for monitoring changes over time in T50.

Indexed as

Renal Insufficiency, ChronicVascular CalcificationBiomarkersCalcium PhosphatesCitratesDialysis SolutionsHumansMagnesiumSpironolactoneBiomarkersCalcium PhosphatesCitratesDialysis SolutionsMagnesiumSpironolactonecalcificationchronic kidney diseaseserum calcification propensity testT50

Identifiers

PMID36136575
PMCPMC9501050
OpenAlexW4296282352

What OpenQuestion holds

Textmetadata
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.