Evidence map›Paper›PMID 42141295›Full record

ArticlePediatric nephrology (Berlin, Germany)2026

Relapsing childhood steroid sensitive nephrotic syndrome: what determines eventual remission?

Evgenia Gurevich, Daniel Landau

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Article in Pediatric nephrology (Berlin, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Evgenia GurevichDepartment of Pediatrics, Barzilai University Medical Center, 7830604, Ashkelon, Israel. gurevichjeny@gmail.com.ORCID http://orcid.org/0000-0001-9095-362X
Daniel LandauNephrology Institute, Schneider Children's Medical Center of Israel, Petach Tikva, Israel.ORCID http://orcid.org/0000-0001-6347-7891

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChildhood idiopathic nephrotic syndrome (INS) responds to corticosteroids (CS), but tends to relapse, often requiring steroid sparing agents (SSA). Long standing treatment free remission (LTFR) evolves in most cases, but whether this is related to puberty or disease length is unknown.

methodsWe retrospectively analyzed the computerized database of Israel's largest health maintenance organization. Children with a new INS diagnosis between 2000-2010 were divided into 2 groups according to INS presentation age. Disease length was determined based on CS or SSA use. Children with disease shorter than 1 year or those not reaching LTFR, defined as more than 3 years from last purchase, were excluded.

resultsOut of 1,669,977 eligible children, 608 were diagnosed with INS, 524 relapsed, 174 were excluded, leaving 350 for analysis: 272 (77.7%) and 78 (22.2%) presented between 2-6.9 and 7-9.9 years, respectively. There was no difference in the need for SSA, time to SSA initiation and drug purchase count between the groups. After 15.5 ± 5.1 years of follow up, time until LTFR was longer in the older group (5.4 ± 4 vs. 7.1 ± 5.1 years, p = 0.002), without correlation between INS onset age and disease length. Many patients, especially in the older group, still relapsed beyond Tanner stage 3's 97th percentile age (age 14 years) (14.7% vs. 51.3%, p < 0.001), irrelevant of sex.

conclusionsIn this population-based study LTFR occurred in many cases well beyond puberty, in both groups, favoring the role for disease length on LTFR, probably due to maturational immune system changes.

Indexed as

Adrenal Cortex HormonesGlucocorticoidsNephrotic SyndromeAdolescentAge FactorsAge of OnsetChildChild, PreschoolFemaleFollow-Up StudiesHumansIsraelMalePubertyRecurrenceRemission InductionAdrenal Cortex HormonesGlucocorticoidsDisease lengthIdiopathic nephrotic syndromePubertySpontaneous remission

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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.