Evidence map›Paper›PMID 37052692›Full record

Observational studyPediatric nephrology (Berlin, Germany)2023

Changes in bone turnover markers after discontinuing long-term glucocorticoid administration in children with idiopathic nephrotic syndrome: a multicenter retrospective observational study.

Yasuhiro Ueda, Takayuki Okamoto, Yasuyuki Sato, Asako Hayashi, Toshiyuki Takahashi, Ryota Suzuki, Hayato Aoyagi, Michihiko Ueno, Norio Kobayashi, Kimiaki Uetake and 3 more

Abstract readObservational StudyMulticenter Study
PubMed Publisher
In one paragraph

Observational study in Pediatric nephrology (Berlin, Germany), 2023. 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, top 67% 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

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. 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

13 authors at 6 institutions in 1 country.

Yasuhiro UedaDepartment of Pediatrics, Hokkaido University Graduate School of Medicine, North 15, West 7, Sapporo, Hokkaido, Japan.ORCID http://orcid.org/0000-0003-4205-320X
Takayuki OkamotoDepartment of Pediatrics, Hokkaido University Graduate School of Medicine, North 15, West 7, Sapporo, Hokkaido, Japan. okamon@med.hokudai.ac.jp.ORCID http://orcid.org/0000-0002-6029-451X
Yasuyuki SatoDepartment of Pediatrics, Hokkaido University Graduate School of Medicine, North 15, West 7, Sapporo, Hokkaido, Japan.ORCID http://orcid.org/0000-0002-7804-5490
Asako HayashiDepartment of Pediatrics, Hokkaido University Graduate School of Medicine, North 15, West 7, Sapporo, Hokkaido, Japan.ORCID http://orcid.org/0000-0002-9023-0904
Toshiyuki TakahashiDepartment of Pediatrics, Hokkaido University Graduate School of Medicine, North 15, West 7, Sapporo, Hokkaido, Japan.ORCID http://orcid.org/0000-0002-8783-3528
Ryota SuzukiDepartment of Pediatrics, Hokkaido University Graduate School of Medicine, North 15, West 7, Sapporo, Hokkaido, Japan.ORCID http://orcid.org/0000-0002-3021-8348
Hayato AoyagiDepartment of Pediatrics, Obihiro Kyokai Hospital, Obihiro, Hokkaido, Japan.
Michihiko UenoDepartment of Pediatrics, Nikko Memorial Hospital, Muroran, Hokkaido, Japan.ORCID http://orcid.org/0000-0002-6542-3173
Norio KobayashiDepartment of Pediatrics, Oji General Hospital, Tomakomai, Hokkaido, Japan.
Kimiaki UetakeDepartment of Pediatrics, Obihiro Kosei Hospital, Obihiro, Hokkaido, Japan.
Masanori NakanishiDepartment of Pediatrics, Kushiro Red Cross Hospital, Kushiro, Hokkaido, Japan.
Tadashi ArigaDepartment of Pediatrics, Hokkaido University Graduate School of Medicine, North 15, West 7, Sapporo, Hokkaido, Japan.
Atsushi ManabeDepartment of Pediatrics, Hokkaido University Graduate School of Medicine, North 15, West 7, Sapporo, Hokkaido, Japan.ORCID http://orcid.org/0000-0002-6698-2348
Hokkaido University · JPKushiro Rosai Hospital · JPNikko Memorial Hospital · JPObihiro Kosei General Hospital · JPObihiro National Hospital · JPOji General Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGlucocorticoids affect bone turnover. Little is known about how bone turnover changes when glucocorticoids are discontinued following long-term administration.

methodsThis retrospective observational study was conducted on the relationship between discontinuation of long-term administration of glucocorticoid and bone turnover markers (BTMs) in patients with childhood-onset idiopathic nephrotic syndrome. Serum bone alkaline phosphatase (BAP), intact procollagen type 1 N-terminal propeptide (P1NP), and tartrate-resistant acid phosphatase-5b (TRACP-5b) were evaluated as BTMs.

resultsThirty-eight pairs of BTMs at glucocorticoid administration and after discontinuation were analyzed in 29 patients. The median age at baseline was 12.4 (interquartile range, 9.0-14.5) years, and the median time from the onset of nephrotic syndrome was 5.9 (3.3-9.7) years. The mean period from prednisolone discontinuation to the measurement of BTMs after glucocorticoid discontinuation was 3.5 ± 1.0 months. Changes in BTMs after glucocorticoid discontinuation were modest when the daily prednisolone dose was < 0.25 mg/kg/day (ln BAP standard deviation [SD] score, p = 0.19; log intact P1NP SD score, p = 0.70; TRACP-5b, p = 0.95). When the daily prednisolone dose was ≥ 0.25 mg/kg/day, all BTMs increased significantly after glucocorticoid discontinuation (ln BAP SD score, p < 0.01; log intact P1NP SD score, p < 0.01; TRACP-5b, p < 0.01).

conclusionsDecreased BTMs can rise within a few months of discontinuing long-term glucocorticoid administration. When the administered glucocorticoid dose is low, changes in BTMs may be small. A higher resolution version of the Graphical abstract is available as Supplementary information.

Indexed as

GlucocorticoidsNephrotic SyndromeAlkaline PhosphataseBiomarkersBone DensityBone RemodelingChildHumansPrednisoloneTartrate-Resistant Acid PhosphataseAlkaline PhosphataseBiomarkersGlucocorticoidsPrednisoloneTartrate-Resistant Acid PhosphataseBone turnover markersChildrenGlucocorticoidNephrotic syndromeRituximab

Identifiers

PMID37052692
OpenAlexW4365443825

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.