Evidence map›Paper›PMID 23314441›Full record

Trial reportPediatric nephrology (Berlin, Germany)2013

Prospective 5-year follow-up of cyclosporine treatment in children with steroid-resistant nephrosis.

Yuko Hamasaki, Norishige Yoshikawa, Hitoshi Nakazato, Satoshi Sasaki, Kazumoto Iijima, Koichi Nakanishi, Takeshi Matsuyama, Kenji Ishikura, Shuichi Ito, Tetsuji Kaneko and 2 more

Abstract readClinical TrialMulticenter Study
PubMed Publisher
In one paragraph

Trial report in Pediatric nephrology (Berlin, Germany), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 9% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Guideline
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  4. [Efficacy and safety of rituximab in children with refractory nephrotic syndrome].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2026
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  10. Review
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  17. AKI in Children Hospitalized with Nephrotic Syndrome.Clinical journal of the American Society of Nephrology : CJASN · 2015
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  18. Article
  19. Spectrum of steroid-resistant and congenital nephrotic syndrome in children: the PodoNet registry cohort.Clinical journal of the American Society of Nephrology : CJASN · 2015
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 1 country.

Yuko HamasakiDepartment of Nephrology, Tokyo Metropolitan Children's Medical Center, Fuchu, Japan. yuhamasaki@med.toho-u.ac.jp
Norishige Yoshikawa
Hitoshi Nakazato
Satoshi Sasaki
Kazumoto Iijima
Koichi Nakanishi
Takeshi Matsuyama
Kenji Ishikura
Shuichi Ito
Tetsuji Kaneko
Masataka Honda
for Japanese Study Group of Renal Disease in Children
Tokyo Metropolitan Children's Medical Center · JPWakayama Medical University · JPHokkaido University · JPNational Center For Child Health and Development · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCyclosporine has improved remission rates in children with steroid-resistant nephrotic syndrome (SRNS). However, little prospective long-term follow-up data is available.

methodsWe prospectively followed and analyzed 5-year outcomes of all 35 patients enrolled in our previous prospective multicenter trial with cyclosporine and steroids in children with SRNS. At enrollment, 23 cases were classified as minimal change (MC), five as diffuse mesangial proliferation (DMP), and seven as focal segmental glomerulosclerosis (FSGS).

resultsRenal survival at 5 years (median 7.7 years) was 94.3 %. Patient status was complete remission (CR) in 31 (88.6 %) (MC/DMP, 25; FSGS, 6); partial remission in one (FSGS); and non-remission in three (MC/DMP), including chronic kidney disease and end-stage kidney disease in one each. Among 31 patients with CR, 22 (71.0 %) were receiving treatment with immunosuppressants at 5 years, including cyclosporine in 19, and seven of these 22 continued to show frequent relapse. Response to cyclosporine at 4 months predicted 5-year outcome in 31 of 35 patients.

conclusionsAlthough SRNS treatment with cyclosporine provides high renal survival and remission rates, many children require ongoing immunosuppression. Management has advanced from the prevention of end-stage kidney disease to the long-term maintenance of remission and management of relapse after induction therapy.

Indexed as

AdolescentChildCyclosporineDisease ProgressionDrug Therapy, CombinationFemaleFollow-Up StudiesGlomerulosclerosis, Focal SegmentalHumansImmunosuppressive AgentsJapanKidneyKidney Failure, ChronicMaleMethylprednisoloneNephrosis, LipoidCyclosporineImmunosuppressive AgentsMethylprednisolone

Identifiers

PMID23314441
OpenAlexW2050498243

What OpenQuestion holds

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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.