Evidence map›Paper›PMID 24902941›Full record

ArticlePediatric nephrology (Berlin, Germany)2014

Bone health in children and adolescents with steroid-sensitive nephrotic syndrome assessed by DXA and QUS.

Gabriella Aceto, Olinda D'Addato, Giovanni Messina, Vincenza Carbone, Luciano Cavallo, Giacomina Brunetti, Maria Felicia Faienza

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Article in Pediatric nephrology (Berlin, Germany), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

14 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Observational
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  5. Article
  6. Mechanisms of Bone Impairment in Sickle Bone Disease.International journal of environmental research and public health · 2021
    Review
  7. Article
  8. Bone Health in Glomerular Kidney Disease.Current osteoporosis reports · 2019
    Review
  9. Article
  10. Article
  11. Skeletal status assessment by quantitative ultrasound and bone densitometry in children with different renal conditions.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2018
    Article
  12. Article
  13. Article
  14. 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

7 authors at 3 institutions in 2 countries.

Gabriella AcetoDivision of Pediatric Nephrology, Children's Hospital Giovanni XXIII, Bari, Italy.
Olinda D'Addato
Giovanni Messina
Vincenza Carbone
Luciano Cavallo
Giacomina Brunetti
Maria Felicia Faienza
University of Bari Aldo Moro · ITBoston Children's Hospital · USOspedale Pediatrico Giovanni XXIII · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe management of steroid-sensitive nephrotic syndrome (SSNS) requires treatment with high-dose glucocorticoids (GCs), but GC usage causes the most frequent form of drug-induced osteoporosis. The aim of our study was to evaluate the impact of GCs on bone mineralization in patients with SSNS using two diagnostic tools, dual-energy X-ray densitometry (DXA) and quantitative ultrasound (QUS), and to compare the diagnostic efficacy of these two imaging tools.

methodsA total of 30 children with SSNS (age 5.20 ± 2.20 years) were evaluated at the start (T0) and after 1 (T1), 2.44 ± 0.75 (T2, 18 patients) and 5.96 ± 2.33 years (T4, 12 patients) of GC treatment. Patients who stopped at T2 were also evaluated at the 1-year timepoint after ceasing GC treatment (T3).

resultsOf the patients assessed at T2, 11 had bone mineralization at the lower limit of normal versus those at T0 and T1, with bone mineralization rescue at the 1-year timepoint after GC discontinuation. At T4, 6/12 patients had densitometric parameters at the lower limit of normal values, and 3/12 patients showed reduced bone mineralization. The parameters derived from measurements of DXA and QUS were significantly related to each timepoint.

conclusionsPatients with SSNS receiving GC therapy undergo bone status alteration related to the dosage and duration of the therapy. In terms of diagnostic efficacy, DXA and QUS were comparable, indicating that QUS is a reliable tool to evaluate bone health in children with SSNS.

Indexed as

Absorptiometry, PhotonAdolescentAnti-Inflammatory AgentsBone and BonesCalcification, PhysiologicChildChild, PreschoolFemaleGlucocorticoidsHumansInfantMaleNephrotic SyndromeOsteoporosisPubertySteroidsAnti-Inflammatory AgentsGlucocorticoidsSteroids

Identifiers

PMID24902941
OpenAlexW1984656479

What OpenQuestion holds

Textmetadata
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.