Evidence map›Paper›PMID 24763863›Full record

ArticleClinical journal of the American Society of Nephrology : CJASN2014

Expression of fibroblast growth factor 23, vitamin D receptor, and sclerostin in bone tissue from hypercalciuric stone formers.

Viviane Barcellos Menon, Rosa Maria Affonso Moysés, Samirah Abreu Gomes, Aluizio Barbosa de Carvalho, Vanda Jorgetti, Ita Pfeferman Heilberg

Open access · greenAbstract read
In one paragraph

Article in Clinical journal of the American Society of Nephrology : CJASN, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

12 citing papers in PubMed, 22 citations in OpenAlex.

  1. Role of FGF23 in Pediatric Hypercalciuria.BioMed research international · 2017
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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 at 2 institutions in 1 country.

Viviane Barcellos MenonNephrology Division, Federal University of São Paulo, São Paulo, Brazil; and.
Rosa Maria Affonso MoysésNephrology Division, University of São Paulo, São Paulo, Brazil.
Samirah Abreu GomesNephrology Division, Federal University of São Paulo, São Paulo, Brazil; and.
Aluizio Barbosa de CarvalhoNephrology Division, Federal University of São Paulo, São Paulo, Brazil; and.
Vanda JorgettiNephrology Division, University of São Paulo, São Paulo, Brazil.
Ita Pfeferman HeilbergNephrology Division, Federal University of São Paulo, São Paulo, Brazil; and ita.heilberg@gmail.com.
Universidade Federal de São Paulo · BRUniversidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesIncreased bone resorption, low bone formation, and abnormal mineralization have been described in stone formers with idiopathic hypercalciuria. It has been previously shown that the receptor activator of NF-κB ligand mediates bone resorption in idiopathic hypercalciuria (IH). The present study aimed to determine the expression of fibroblast growth factor 23 (FGF-23), vitamin D receptor (VDR), and sclerostin in bone tissue from IH stone formers. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: Immunohistochemical analysis was performed in undecalcified bone samples previously obtained for histomorphometry from 30 transiliac bone biopsies of idiopathic hypercalciuria stone-forming patients between 1992 and 2002 and 33 healthy individuals (controls). Serum parameters were obtained from their medical records.

resultsHistomorphometry disclosed 21 IH patients with high and 9 IH patients with normal bone resorption. Importantly, eroded surfaces (ES/BS) from IH patients but not controls were significantly correlated with VDR immunostaining in osteoblasts (r=0.51; P=0.004), sclerostin immunostaining in osteocytes (r=0.41; P=0.02), and serum 1,25-dihydroxyvitamin D (r=0.55; P<0.01). Of note, both VDR and sclerostin immunostaining were significantly correlated with serum 1,25-dihydroxyvitamin D in IH patients (r=0.52; P=0.01 and r=0.53; P=0.02, respectively), although VDR and sclerostin expression did not differ between IH and controls. IH patients with high bone resorption exhibited a significantly stronger sclerostin immunostaining than IH patients with normal bone resorption. FGF-23 expression in osteocytes from IH patients did not differ from controls and was not correlated with any histomorphometric parameter.

conclusionsThese findings suggest the contribution of VDR and sclerostin, as well as 1,25-dihydroxyvitamin D, to increase bone resorption in idiopathic hypercalciuria but do not implicate FGF-23 in the bone alterations seen in these patients.

Indexed as

Adaptor Proteins, Signal TransducingAdultBone Morphogenetic ProteinsBone ResorptionFemaleFibroblast Growth Factor-23Fibroblast Growth FactorsGenetic MarkersHumansHypercalciuriaIliumImmunohistochemistryMaleMiddle AgedOsteoblastsOsteocytes1,25-dihydroxyvitamin DAdaptor Proteins, Signal TransducingBone Morphogenetic ProteinsFGF23 protein, humanFibroblast Growth Factor-23Fibroblast Growth FactorsGenetic MarkersReceptors, CalcitriolSOST protein, humanVDR protein, humanVitamin DFGF-23hypercalciuriaimmunohistochemistrysclerostinVDR

Identifiers

PMID24763863
PMCPMC4078962
OpenAlexW2130592591

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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.